Find where to buy products from suppliers in the USA, including: distributors, industrial manufacturers in America, bulk supplies and wholesalers of raw ingredients & finished goods.
Search for products or services, then visit the American suppliers website for prices, SDS or more information. You can also view suppliers in Australia, NZ or the UK.
| Product | Description | |
|---|---|---|
| Triphenyl phosphine | Triphenyl phosphine. Group: Biochemicals. Grades: Highly Purified. CAS No. 603-35-0. Pack Sizes: 250g, 500g, 1kg, 2kg, 5kg. Molecular Formula: C18H15P. US Biological Life Sciences. |  Worldwide |
| Bis(triphenylphosphine)iminium chloride | suzuki reaction. Group: Other phosphine ligands. Alternative Names: Bis (triphenylphosphoranylidene)ammonium chloride; PPNCl, Hexaphenyldiphosphazenium chloride. CAS No. 21050-13-5. Molecular formula: C36H30ClNP2. Mole weight: 574.03. Appearance: Solid. Purity: 0.98. IUPACName: triphenyl-[(triphenyl-lambda5-phosphanylidene)amino]phosphanium; chloride. Canonical SMILES: C1=CC=C (C=C1)P (=N[P+] (C2=CC=CC=C2) (C3=CC=CC=C3)C4=CC=CC=C4) (C5=CC=CC=C5)C6=CC=CC=C6. [Cl-]. ECNumber: 258-552-5. Catalog: ACM21050135-1. |  |
| Bis(triphenylphosphine)nickel(II) dichloride | dichloridobis (triphenylphosphane)nickel (II) is a metal phosphine complex with the formula NiCl2[P(C6H5)3]2. It is a dark blue crystalline solid. It is used as a catalyst for organic synthesis. Uses: Ni(pph3)2cl2 may be used to undertake nickel assisted phosphination of biaryl o,n triflates with chlorodiphenylphosphine. Group: Vapor deposition precursorspolymerization reagents. Alternative Names: Dichlorobis (triphenylphosphine)nickel (II), NiCl2(PPh3)2, Nickel(II)bis(triphenylphosphine) dichloride. CAS No. 14264-16-5. Pack Sizes: 10 g in glass bottle. Product ID: dichloronickel; triphenylphosphane. Molecular formula: 654.17. Mole weight: C36H32Cl2NiP2-. Cl[Ni]Cl. c1ccc(cc1)P(c2ccccc2)c3ccccc3. c4ccc(cc4)P(c5ccccc5)c6ccccc6. 1S/2C18H15P. 2ClH. Ni/c2*1-4-10-16 (11-5-1) 19 (17-12-6-2-7-13-17) 18-14-8-3-9-15-18; ; ; /h2*1-15H; 2*1H; /q; ; ; ; +2/p-2, ZBRJXVVKPBZPAN-UHFFFAOYSA-L. ZBRJXVVKPBZPAN-UHFFFAOYSA-L. |  |
| Bis(triphenylphosphine)palladium(II) Diacetate | suzuki reaction. Group: Palladium series catalysts. Alternative Names: bis(triphenyl phosphine)palladium(II) acetate; M-7910; AC1L37OG; bis(triphenylphosphine) palladium(II)acetate; Palladium, bis(acetato-kO)bis(triphenylphosphine)- (9CI); EINECS 238-628-4; AKOS015898550; bis(triphenylphosphine)-palladium (II) acetate; palladium(2+); I10-0287. CAS No. 14588-08-0. Molecular formula: C40H36O4P2Pd. Mole weight: 749.092g/mol. IUPACName: palladium(2+); triphenylphosphane; diacetate. Canonical SMILES: CC (=O)[O-]. CC (=O)[O-]. C1=CC=C (C=C1)P (C2=CC=CC=C2)C3=CC=CC=C3. C1=CC=C (C=C1)P (C2=CC=CC=C2)C3=CC=CC=C3. [Pd+2]. ECNumber: 238-628-4. Catalog: ACM14588080. | |
| Bromotris(triphenylphosphine)rhodium | Rhodium-catalyzed regio- and stereoselective addition of diphenylphosphine oxide to alkynes. Rhodium- catalyzed hydrophosphinylation. Group: Rhodium series of catalysts. Alternative Names: bromide; Bromotris (triphenylphosphine)rhodium; EINECS 239-050-5; Bromotris (triphenylphosphine)rhodium (I); Jsp002843; phosphine, triphenyl-, bromide, rhodium salt(3:1); RL01906; AC1Q1R7U; triphenylphosphane. CAS No. 14973-89-8. Molecular formula: C54H45BrP3Rh-. Mole weight: 969.685g/mol. IUPACName: rhodium;triphenylphosphane;bromide. Canonical SMILES: C1=CC=C (C=C1)P (C2=CC=CC=C2)C3=CC=CC=C3. C1=CC=C (C=C1)P (C2=CC=CC=C2)C3=CC=CC=C3. C1=CC=C (C=C1)P (C2=CC=CC=C2)C3=CC=CC=C3. [Br-]. [Rh]. ECNumber: 239-050-5. Catalog: ACM14973898. | |
| Cyclopentadienylbis (triphenylphosphine) ruthenium Chloride | Cyclopentadienylbis (triphenylphosphine) ruthenium Chloride. Group: Biochemicals. Alternative Names: η 5-Cyclopentadienylbis (triphenylphosphine) ruthenium Chloride; , Chloro-?-cyclopentadienylbis (triphenylphosphine) Ruthenium; Bis (tri phenyl phosphine) (chloro) cyclopentadienyl ruthenium ; Bis (triphenylphosphine) (cyclopentadiene) ruthenium chloride; Bis (tri phenyl phosphine) cyclopentadienyl ruthenium chloride; Chloro (cyclopentadienyl) bis (triphenylphosphine) ruthenium; Chloro (cyclopentadienyl) bis (triphenylphosphine) ruthenium (II) ; Chloro (η -cyclopentadienyl) bis (triphenylphosphine) ruthenium; Chloro (η 5-2, 4-cyclopentadien-1-yl) bis (triphenylphosphine) ruthenium; Chloro (η 5-cyclopentadienyl) bis (triphenylphosphine) ruthenium; Chloro-?-cyclopentadienylbis (triphenylphosphine) ruthenium. Grades: Highly Purified. CAS No. 32993-05-8. Pack Sizes: 1g. Molecular Formula: C41H35ClP2Ru, Molecular Weight: 726.19. US Biological Life Sciences. | Worldwide |
| N-(β-D-glucopyranosyl)triphenyl-phosphine imide | N-(β-D-glucopyranosyl)triphenyl-phosphine imide, a chemical compound with intriguing potential, has garnered significant interest in the medical industry to treat complex diseases like cancer and diabetes. Its compositions unique nature enables it to be utilized for targeted pharmaceutical delivery and enhanced efficacy. Preliminary testing in preclinical studies displays remarkably encouraging results. As such, this compound proves to be a promising candidate for further investigations in its therapeutic applications. Synonyms: (2R, 3S, 4S, 5R, 6R) -2- (Hydroxymethyl) -6- ( (triphenylphosphoranylidene) amino) tetrahydro-2H-pyran-3, 4, 5-triol; beta-D-Glucopyranosylamine, N-(triphenylphosphoranylidene)-; N-(-D-glucopyranosyl)triphenylphosphine imide. Grades: 98%. CAS No. 100639-11-0. Molecular formula: C24H26NO5P. Mole weight: 439.44. |  |
| Poly(ethylene glycol) triphenylphosphine | Poly(ethylene glycol) triphenylphosphine can be used as a hydrogenation catalyst in a water/substrate two-phase medium. Group: Other phosphine ligands. Alternative Names: Poly(ethylene glycol) triphenylphosphine;238403-28-6. CAS No. 238403-28-6. Molecular formula: C20H21O2P. Mole weight: 324.36g/mol. IUPACName: ethane-1,2-diol;triphenylphosphane. Canonical SMILES: C1=CC=C (C=C1)P (C2=CC=CC=C2)C3=CC=CC=C3. C (CO)O. Catalog: ACM238403286. | |
| Triphenylphosphine | In organic synthesis; polymerization initiator. Group: Other phosphine ligandscoupling. Alternative Names: SCHEMBL1679860; triphenyl phophine; Trifenylfosfin; Triphenyl phosphine; Triphenylphosphine, ReagentPlus(R), 99%; 7817AH; Triphenyl phosphine pound>>Triphenyl phosphorous; Copolymer of styrene and divinylbenzene, diphenylphosphinated; Triphenylphosphine, ReagentPlus(R), >=98.5%. CAS No. 603-35-0. Molecular formula: C18H15P;(C6H5)3P;C18H15P. Mole weight: 262.292g/mol. IUPACName: triphenylphosphane. Canonical SMILES: C1=CC=C (C=C1)P (C2=CC=CC=C2)C3=CC=CC=C3. Density: 1.194 at 77 ° F (NTP, 1992);1.075 @ 80 DEG C/4 DEG C;1.1 g/cm3. ECNumber: 238-154-8. Catalog: ACM603350. | |
| Triphenylphosphine | Triphenylphosphine is a member of the class of tertiary phosphines that is phosphane in which the three hydrogens are replaced by phenyl groups. It has a role as a reducing agent. It is a member of benzenes and a tertiary phosphine. CAS No. 603-35-0. Product ID: PE-0666. Molecular formula: C18H15P. Category: Synthetic catalyst. Product Keywords: Catalysts; Triphenylphosphine; PE-0666; Synthetic catalyst; C18H15P; 603-35-0. Color: White. EC Number: 210-036-0. Physical State: Crystals, Crystalline Powder or Flakes. Solubility: water: soluble0.00017 g/L at 22°C. Storage: Store below +30°C. Applications: Triphenylphosphine is used as a polymerization initiator and an intermediate to make pharmaceuticals, phosphonium salts, and other phosphorus compounds. Boiling Point: 377 °C(lit.). Melting Point: 79-81 °C(lit.). Density: 1.132. Product Description: Triphenylphosphine is used as a polymerization initiator and an intermediate to make pharmaceuticals, phosphonium salts, and other phosphorus compounds. |  |
| Triphenylphosphine | Triphenylphosphine. Uses: In organic synthesis; polymerization initiator. Group: Polymerization reagents. Alternative Names: SCHEMBL1679860; triphenyl phophine; Trifenylfosfin; Triphenyl phosphine; Triphenylphosphine, ReagentPlus(R), 99%; 7817AH; Triphenyl phosphine pound>>Triphenyl phosphorous; Copolymer of styrene and divinylbenzene, diphenylphosphinated; Triphenylphosphine, ReagentPlus(R), >=98.5%. CAS No. 603-35-0. Product ID: triphenylphosphane. Molecular formula: 262.292g/mol. Mole weight: C18H15P;(C6H5)3P;C18H15P. C1=CC=C (C=C1)P (C2=CC=CC=C2)C3=CC=CC=C3. InChI=1S/C18H15P/c1-4-10-16 (11-5-1) 19 (17-12-6-2-7-13-17) 18-14-8-3-9-15-18/h1-15H. RIOQSEWOXXDEQQ-UHFFFAOYSA-N. | |
| Triphenylphosphine oxide | Flame Retardant. Alternative Names: Phosphine oxide, triphenyl-; Triphenyl phosphorus oxide; (C6H5)3P=O; Triphenylphosphanoxid; Triphenylphosphanoxide; (C6H5)3PO;Triphenylphosphine oxide;Triphenyl phosphorus oxide. CAS No. 791-28-6. Molecular formula: C18H15OP. Mole weight: 278.28. Appearance: Solid. Purity: 0.99. IUPACName: diphenylphosphorylbenzene. Canonical SMILES: C1=CC=C (C=C1)P (=O) (C2=CC=CC=C2)C3=CC=CC=C3. Density: 1.212 g/cm3. ECNumber: 212-338-8. Catalog: ACM791286-1. | |
| Triphenylphosphine oxide | Triphenylphosphine oxide. Uses: Flame retardant. Group: Ligands for functional metal complexes. Alternative Names: Phosphine oxide, triphenyl-; Triphenyl phosphorus oxide; (C6H5)3P=O; Triphenylphosphanoxid; Triphenylphosphanoxide; (C6H5)3PO; Triphenylphosphine oxide; Triphenyl phosphorus oxide. CAS No. 791-28-6. Product ID: diphenylphosphorylbenzene. Molecular formula: 278.28. Mole weight: C18H15OP. C1=CC=C (C=C1)P (=O) (C2=CC=CC=C2)C3=CC=CC=C3. 1S/C18H15OP/c19-20 (16-10-4-1-5-11-16, 17-12-6-2-7-13-17) 18-14-8-3-9-15-18/h1-15H. FIQMHBFVRAXMOP-UHFFFAOYSA-N. 99%. | |
| Triphenylphosphine, polymer-bound | Triphenylphosphine resin is used for the preparation of polymer bound ylids which are useful for Wittig reactions. Group: Heterocyclic organic compound. Alternative Names: Triphenylphosphine, flakes; CHEMBL1448331; 39319-11-4; P(C6H5)3; 58079-51-9; triphenyl phosphin; NCGC00259663-01; ZX-AT007677; FT-0689298; Triphenylphosphine, powder. CAS No. 39319-11-4. Molecular formula: C18H15P;(C6H5)3P;C18H15P. Mole weight: 262.292g/mol. IUPACName: triphenylphosphane. Canonical SMILES: C1=CC=C (C=C1)P (C2=CC=CC=C2)C3=CC=CC=C3. Density: 1.194 at 77 ° F (NTP, 1992);1.075 @ 80 DEG C/4 DEG C;1.1 g/cm³. ECNumber: 238-154-8. Catalog: ACM39319114. | |
| (2,4-Dichlorobenzyl)triphenylphosphonium Chloride | suzuki reaction. Group: Organic phosphine compounds. Alternative Names: Triphenyl(2,4-dichlorobenzyl)phosphonium Chloride. CAS No. 2492-23-1. Molecular formula: C25H20Cl3P. Mole weight: 457.76. Appearance: Solid. Purity: 0.98. IUPACName: (2,4-dichlorophenyl)methyl-triphenylphosphanium;chloride. Canonical SMILES: C1=CC=C (C=C1)[P+] (CC2=C (C=C (C=C2)Cl)Cl) (C3=CC=CC=C3)C4=CC=CC=C4. [Cl-]. ECNumber: 219-659-2. Catalog: ACM2492231-1. | |
| (3-Bromopropyl)triphenylphosphonium bromide | (3-Bromopropyl)triphenylphosphonium Bromide is used in rearrangement reactions of cyclic organic molecules and in organic synthesis. Group: Organic phosphine compounds. Alternative Names: I01-9357; 3-bromopropyl(triphenyl)phosphonium bromide; NSC84074; MFCD00011866; (3-Bromo-propyl)-triphenyl-phosphonium bromide; 3-(Bromopropyl)triphenylphosphonium; EINECS 222-770-9; Bromo(3-bromopropyl)triphenylphosphorus; FT-0604703; Acm³607178. CAS No. 3607-17-8. Molecular formula: C21H21Br2P. Mole weight: 464.18. Appearance: Solid. Purity: 0.98. IUPACName: 3-bromopropyl(triphenyl)phosphanium; bromide. Canonical SMILES: C1=CC=C (C=C1)[P+] (CCCBr) (C2=CC=CC=C2)C3=CC=CC=C3. [Br-]. ECNumber: 222-770-9. Catalog: ACM3607178-1. | |
| 4- (Di methyl amino) phenyl diphenyl phosphine | 4- (Di methyl amino) phenyl diphenyl phosphine. Group: Biochemicals. Alternative Names: 4- (Dimethylamino) triphenylphosphine; 4-(Diphenylphosphino)-N,N-dimethylaniline. Grades: Highly Purified. CAS No. 739-58-2. Pack Sizes: 2g, 5g, 10g, 25g, 50g. US Biological Life Sciences. | Worldwide |
| 5-Carboxypentyl triphenylphosphonium bromide | (5-Carboxypentyl)(triphenyl)phosphonium bromide is used in medicine and as pharmaceutical intermediate. It is also employed as catalyst. Reactant for: Preparation of inhibitor of protein tyrosine phosphatase 1B for treatment of diabetes and obesity. Synthesis of folate receptor-specific glycinamide ribonucleotide formyltransferase inhibitors with antitumor activity. Preparation of peptide nucleic acids (PNA) with high specific activity. Synthesis of roseophilin via Wittig/aldol methodology. Group: Organic phosphine compounds. Alternative Names: (5-Carboxypentyl)(Triphenyl)Phosphonium Bromide. CAS No. 50889-29-7. Molecular formula: C24H26BrO2P. Mole weight: 457.35. Appearance: Solid. Purity: 0.98. IUPACName: 5-carboxypentyl(triphenyl)phosphanium; bromide. Canonical SMILES: C1=CC=C (C=C1)[P+] (CCCCCC (=O)O) (C2=CC=CC=C2)C3=CC=CC=C3. [Br-]. Catalog: ACM50889297-3. | |
| (Carbethoxymethyl) triphenylphosphonium bromide | suzuki reaction. Group: Organic phosphine compounds. Alternative Names: (Ethoxycarbonylmethyl) triphenylphosphonium bromide; (Carboxymethyl)triphenylphosphonium bromide ethyl ester. CAS No. 1530-45-6. Molecular formula: C22H22BrO2P. Mole weight: 429.29. Appearance: Solid. Purity: 0.98. IUPACName: (2-ethoxy-2-oxoethyl)-triphenylphosphanium; bromide. Canonical SMILES: CCOC (=O)C[P+] (C1=CC=CC=C1) (C2=CC=CC=C2)C3=CC=CC=C3. [Br-]. ECNumber: 216-230-1. Catalog: ACM1530456-2. | |
| Ethyl (triphenylphosphoranylidene)acetate | A common Wittig reagent. A cholinesterase inhibitor. Group: Other phosphine ligands. Alternative Names: (Carbethoxymethylene) Triphenylphosphorane; Triphenylcarbethoxy methyl enephosphorane. CAS No. 1099-45-2. Molecular formula: C22H21O2P. Mole weight: 348.37. Appearance: Solid. Purity: 0.97. IUPACName: ethyl 2-(triphenyl-lambda5-phosphanylidene)acetate. Canonical SMILES: CCOC (=O)C=P (C1=CC=CC=C1) (C2=CC=CC=C2)C3=CC=CC=C3. Density: 1.086 g/cm3. ECNumber: 214-151-7. Catalog: ACM1099452-1. | |
| I-propyl triphenylphosphonium iodide | Isopropyltriphenylphosphonium Iodide is a synthetic reagent used in various olfeination and chiral-auxiliary-mediated synthesis of pharmaceutical goods. Group: Organic phosphine compounds. Alternative Names: (1-Methylethyl)triphenylphosphonium iodide; (2-Propyl)triphenylphosphonium iodide. CAS No. 24470-78-8. Molecular formula: C21H22IP. Mole weight: 432.28. Appearance: Solid. Purity: 0.98. IUPACName: triphenyl(propan-2-yl)phosphanium;iodide. Canonical SMILES: CC (C)[P+] (C1=CC=CC=C1) (C2=CC=CC=C2)C3=CC=CC=C3. [I-]. ECNumber: 246-281-5. Catalog: ACM24470788-2. | |
| Methyltriphenylphosphonium iodide | suzuki reaction. Group: Organic phosphine compounds. Alternative Names: Triphenylmethylphosphine iodide. CAS No. 2065-66-9. Molecular formula: C19H18PI. Mole weight: 404.22. Appearance: Solid. Purity: 0.98. IUPACName: methyl(triphenyl)phosphanium;iodide. Canonical SMILES: C[P+] (C1=CC=CC=C1) (C2=CC=CC=C2)C3=CC=CC=C3. [I-]. ECNumber: 218-178-5. Catalog: ACM2065669-1. | |
| P-Xylylenebis(triphenylphosphonium bromide) | suzuki reaction. Group: Organic phosphine compounds. Alternative Names: (1, 4-Phenylenebis (methylene))bis (triphenylphosphonium) bromide. CAS No. 40817-03-6. Molecular formula: C44H38Br2P2. Mole weight: 788.55. Appearance: Solid. Purity: 98%+. IUPACName: triphenyl-[[4- (triphenylphosphaniumylmethyl) phenyl]methyl]phosphanium; dibromide. Canonical SMILES: C1=CC=C (C=C1)[P+] (CC2=CC=C (C=C2)C[P+] (C3=CC=CC=C3) (C4=CC=CC=C4)C5=CC=CC=C5) (C6=CC=CC=C6)C7=CC=CC=C7. [Br-]. [Br-]. ECNumber: 255-092-7. Catalog: ACM40817036-1. | |
| P-Xylylenebis(triphenylphosphonium chloride) | suzuki reaction. Group: Organic phosphine compounds. Alternative Names: (1, 4-Phenylenebis (methylene))bis (triphenylphosphonium) chloride. CAS No. 1519-47-7. Molecular formula: C44H38Cl2P2. Mole weight: 699.63. Appearance: Solid. Purity: 0.98. IUPACName: triphenyl-[[4- (triphenylphosphaniumylmethyl) phenyl]methyl]phosphanium; dichloride. Canonical SMILES: C1=CC=C (C=C1)[P+] (CC2=CC=C (C=C2)C[P+] (C3=CC=CC=C3) (C4=CC=CC=C4)C5=CC=CC=C5) (C6=CC=CC=C6)C7=CC=CC=C7. [Cl-]. [Cl-]. ECNumber: 216-184-2. Catalog: ACM1519477-1. | |
| (R)-(-)-3,3'-Bis(triphenylsilyl)-1,1'-binaphthyl-2,2'-diyl hydrogen phosphate, min. 98% [(R)-TiPSY] | A chiral phosphoric acid catalyst providing a convenient strategy for the enantioselective construction of protected primary amines and a highly stereoselective method for the reductive amination of heterocyclic amines. Chiral phosphoric acid used for the enantioselective Biginelli and Biginelli-like reactions. Chiral phosphoric acid organocatalyst used in the asymmetric, three-component Povarov reaction involving 2-hydroxystyrenes. An efficient method to access structurally diverse cis-disubstituted tetrahydroquinolines in high stereoselectivities of up to >99:1 dr and 97% ee. A gold/chiral phosphoric acid catalyst used for the highly stereoselective, three-component reaction of salicylaldehydes, anilines, and alkynols to give aromatic spiroacetals in high yields and stereoselectivities. The first highly enantioselective catalytic protocol for the reductive coupling of ketones and hydrozones. Reagent-controlled regioselectivity enabled by dual activation. Group: Organic phosphine compounds. Alternative Names: (S)-(+)-3,3'-Bis(triphenylsilyl)-1,1'-binaphthyl-2,2'-diyl hydrogen phosphate; RD-0080; (11bR)-4-Hydroxy-2,6-bis(triphenylsilyl)dinaphtho-[2,1-d:1 inverted exclamation marka,2 inverted exclamation markaf]-1,3,2-dioxaphosphepin 4-oxide; Carreira SALDIPAC Ligand; (R)-(-)-3,3'-Bis(triphenylsilyl)-1,1'-binaphthyl-2,2'-diyl hydrogen phosp | |
| Triphenyl trithiophosphite | Heterocyclic Organic Compound. Alternative Names: triphenyl trithiophosphite; Tris(phenylthio)phosphine; Trithiophosphorous acid triphenyl ester. CAS No. 1095-04-1. Molecular formula: C18H15PS3. Mole weight: 358.480461. Catalog: ACM1095041. | |
| TSPO1 | TSPO1 is an electon transfer layer (ETL) or hole blocking layer (HBL) in OLED devices. Uses: Tspo1 is a phosphine oxide-based blocking and host material with triplet energy excitons. it is mainly used in the formation of a blocking layer that enhances the performance of organic electronic devices like organic light-emitting diodes (oleds), and delayed fluorescent devices. Group: Organic light emitting diode (oled). Alternative Names: Diphenyl-4-triphenylsilylphenyl-phosphine oxide. CAS No. 1286708-86-8. Molecular formula: C36H29OPSi. Mole weight: 536.67 g/mol. Appearance: Solid. Purity: 95%+. IUPACName: (4-diphenylphosphorylphenyl) -triphenylsilane. Canonical SMILES: C1=CC=C (C=C1)[Si] (C2=CC=CC=C2) (C3=CC=CC=C3)C4=CC=C (C=C4)P (=O) (C5=CC=CC=C5)C6=CC=CC=C6. Catalog: ACM1286708868. | |
| TSPO1 | TSPO1 is an electon transfer layer (ETL) or hole blocking layer (HBL) in OLED devices. Uses: Tspo1 is a phosphine oxide-based blocking and host material with triplet energy excitons. it is mainly used in the formation of a blocking layer that enhances the performance of organic electronic devices like organic light-emitting diodes (oleds), and delayed fluorescent devices. Group: Organic light-emitting diode (oled) materials. Alternative Names: Diphenyl[4- (triphenylsilyl) phenyl]phosphineoxide. CAS No. 1286708-86-8. Product ID: (4-diphenylphosphorylphenyl) -triphenylsilane. Molecular formula: 536.67. Mole weight: C36H29OPSi. C1=CC=C (C=C1)[Si] (C2=CC=CC=C2) (C3=CC=CC=C3)C4=CC=C (C=C4)P (=O) (C5=CC=CC=C5)C6=CC=CC=C6. InChI=1S/C36H29OPSi/c37-38 (30-16-6-1-7-17-30, 31-18-8-2-9-19-31) 32-26-28-36 (29-27-32) 39 (33-20-10-3-11-21-33, 34-22-12-4-13-23-34) 35-24-14-5-15-25-35/h1-29H. TXBFHHYSJNVGBX-UHFFFAOYSA-N. 95%+. | |
| 2-? [ [Hydroxy [ (2R) ?-?2-? [ (1-?oxohexadecyl) ?oxy] ?-?3-? (triphenylmethoxy) ?propoxy] ?phosphinyl] ?oxy] ?-?N, ?N, ?N-?trimethyl-?ethanaminium Inner Salt | 2-? [ [Hydroxy [ (2R) ?-?2-? [ (1-?oxohexadecyl) ?oxy] ?-?3-? (triphenylmethoxy) ?propoxy] ?phosphinyl] ?oxy] ?-?N, ?N, ?N-?trimethyl-?ethanaminium Inner Salt is an intermediate in synthesizing 2-Palmitoyl-sn-glycero-3-phosphocholine (P157350), a food preservative, having the ability to form complexes with starch, retarding its retrodegradation during storage. Group: Biochemicals. Grades: Highly Purified. CAS No. 123231-97-0. Pack Sizes: 5mg, 25mg. Molecular Formula: C43H64NO7P. US Biological Life Sciences. | Worldwide |
| [(2S,6R)-6-{N2-(Isobutyryl)-O6-(diphenylcarbomoyl)guanin-9-yl}-4-tritylmorpholin-2-yl]methyl dimethyl-phosphoramidochloridate | [(2S,6R)-6-{N2-(Isobutyryl)-O6-(diphenylcarbomoyl)guanin-9-yl}-4-tritylmorpholin-2-yl]methyl dimethyl-phosphoramidochloridate, a highly potent chemotherapeutic compound extensively employed in the biomedical industry, showcases exceptional efficiency in the treatment of an array of cancer types. Synonyms: DTXSID301098928; 1357354-76-7; Carbamic acid, N,N-diphenyl-, 9-[ (2R, 6S) -6-[[[chloro (dimethylamino) phosphinyl]oxy]methyl]-4- (triphenylmethyl) -2-morpholinyl]-2-[ (2-methyl-1-oxopropyl) amino]-9H-purin-6-yl ester. CAS No. 1357354-76-7. Molecular formula: C48H48ClN8O6P. Mole weight: 899.37. | |
| 5-[Di(1-adamantyl)phosphino]-1', 3', 5'-triphenyl-1'H-[1, 4']bipyrazole | Other Ligands. Alternative Names: 5-[Di(1-adamantyl)phosphino]-1', 3', 5'-triphenyl-1'H-[1, 4']bipyrazole; 1239478-87-5; 5-[Di(1-adamantyl)phosphino](1,3,5-triphenyl-1H-pyrazol-4-yl)-1H-pyrazole; 5-(di(adamantan-1-yl)phosphino)-1',3',5'-triphenyl-1'H-1,4'-bipyrazole; 5-[Di(1-adamantyl)phosphino]-1', 3', 5'-triphenyl-1, 4'-bi[1H-pyrazole]; ZINC97944277. CAS No. 1239478-87-5. Molecular formula: C44H47N4P. Mole weight: 662.862g/mol. IUPACName: bis(1-adamantyl)-[2-(1,3,5-triphenylpyrazol-4-yl)pyrazol-3-yl]phosphane. Canonical SMILES: C1C2CC3CC1CC (C2) (C3) P (C4=CC=NN4C5=C (N (N=C5C6=CC=CC=C6) C7=CC=CC=C7) C8=CC=CC=C8) C91CC2CC (C9) CC (C2) C1. Catalog: ACM1239478875. | |
Our database is helping our users find suppliers everyday.
