Allyl Methyl Carbonate Suppliers USA
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Product | Description | |
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Allyl methyl carbonate Quick inquiry Where to buy Suppliers range | Allyl methyl carbonate. Group: Polymer/Macromolecule. Alternative Names: CARBONIC ACID ALLYL METHYL ESTER;ALLYL METHYL CARBONATE;Allyl methyl carbonate ,98%;3-(Methoxycarbonyloxy)propene;Carbonic acid O-allyl O-methyl ester;Methyl allyl carbonate;Allyl Methyl carbonate 98%. CAS No. 35466-83-2. Molecular formula: C5H8O3. Mole weight: 116.12. | |
(2-Methylallyl)palladium(II) chloride dimer Quick inquiry Where to buy Suppliers range | yellow powder. Uses: Catalyst for: &bull Asymmetric allylic alkylation reactions &bull Suzuki-Miyaura reactions &bull Reductive cleavage reactions &bull Reaction of alkenyloxiranes with carbon monoxide. Group: Palladium series catalysts. Alternative Names: Chloro(2-methylallyl)palladium(II) dimer. Grades: 0.99. CAS No. 12081-18-4. Molecular formula: [CH2=C(CH3)CH2PdCl]2. Mole weight: 393.94. IUPAC Name: dichloropalladium; 2-methanidylprop-1-ene; palladium(2+). Exact Mass: 501.96400. Symbol: GHS07. Melting Point: 168.2-174.0ºC. InChIKey: CZAHDNZKZMLMCE-UHFFFAOYSA-L. H-Bond Donor: 0. H-Bond Acceptor: 4. Safty Description: 26. Hazard statements: Xi: Irritant. | |
(4R,5R)-(-)-2,2-Dimethyl-α,α,α',α'-tetra(1-naphthyl)-1,3-dioxolane-4,5-dimethanolatotitanium(IV) dichloride acetonitrile adduct Quick inquiry Where to buy Suppliers range | (4R,5R)-(-)-2,2-Dimethyl-α,α,α',α'-tetra(1-naphthyl)-1,3-dioxolane-4,5-dimethanolatotitanium(IV) dichloride acetonitrile adduct. Uses: Catalyst used in the enantioselective fluorination of β-ketoesters. Versatile catalyst used in the enantioselective 1,2 and 1,4 additions to carbonyl compounds, transfer of allyl groups to aldehydes, cycloadditions and others. Group: Heterocyclic Organic Compound. Alternative Names: 197389-47-2;(4R,5R)-(-)-2,2-DIMETHYL-A,A,A',A'-TETRA(1-NAPHTHYL)-1,3-DIOXOLANE-4,5-DIMETHANOLATOTITANIUM(IV) DICHLORIDE ACETONITRILE ADDUCT;MFCD05861615;SC10832;(4R,5R)-(-)-2,2-DIMETHYL-ALPHA,ALPHA,ALPHA',ALPHA'-TETRA(1-NAPHTHYL)-1,3-DIOXOLANE-4,5-DIMETHANOLATOTITANIUM (IV) DICHLORIDE;(4R,5R)-(-)-2,2-DIMETHYL-ALPHA,ALPHA,ALPHA',ALPHA'-TETRA(1-NAPHTHYL)-1,3-DIOXOLANE-4,5-DIMETHANOLATOTITANIUM(IV) DICHLORIDE ACETONITRILE ADDUCT;Titanium,dichloro[2,2-dimethyl-a,a,a',a'-tetra-1-naphthalenyl-1,3-dioxolane-4,5-dimethanolato(2-)-ko4,ko5]-,[t-4-(4r-trans)]-(9ci). CAS No. 197389-47-2. Molecular formula: C49H42Cl2N2O3Ti. Mole weight: 825.653g/mol. IUPAC Name: acetonitrile;dichlorotitanium;[(4R, 5R)-5-[hydroxy(dinaphthalen-1-yl)methyl]-2, 2-dimethyl-1, 3-oxazolidin-4-yl]-dinaphthalen-1-ylmethanol. Rotatable Bond Count: 4. Exact Mass: 824.205g/mol. SMILES: CC#N. CC1 (NC (C (O1)C (C2=CC=CC3=CC=CC=C32) (C4=CC=CC5=CC=CC=C54)O)C (C6=CC=CC7=CC=CC=C76) (C8=CC=CC9=CC=CC=C98)O)C. Cl[Ti]Cl. InChI: InChI=1S/C47H39NO3.C2H3N.2ClH.Ti/c1-45(2)48-43(46(49,39-27-11-19-31-15-3-7-23-35(31)39)40-28-12-20-32-16-4-8-24-36(32)40)44(51-45)47(50,41-29-13-21-33-17-5-9-25-37(33)41)42-30-14-22-34-18-6-10-26-38(34)42;1-2-3;;;/h3-30,43-44,48-50H,1-2H3;1H3;2*1H;/q;;;;+2/p-2/t43-,44-;;;;/m1./s1. InChIKey: WINAMCRSRUMNBX-VCYTWFGNSA-L. H-Bond Donor: 3. H-Bond Acceptor: 5. Monoisotopic Mass: 824.205g/mol. | |
(4R,5R)-(-)-2,2-Dimethyl-α,α,α',α'-tetraphenyl-1,3-dioxolane-4,5-dimethanolato[1,2-bis(dimethoxy)ethane]titanium(IV) dichloride acetonitrile adduct Quick inquiry Where to buy Suppliers range | (4R,5R)-(-)-2,2-Dimethyl-α,α,α',α'-tetraphenyl-1,3-dioxolane-4,5-dimethanolato[1,2-bis(dimethoxy)ethane]titanium(IV) dichloride acetonitrile adduct. Uses: Catalyst used in the enantioselective fluorination of β-ketoesters. Versatile catalyst used in the enantioselective 1,2 and 1,4 additions to carbonyl compounds, transfer of allyl groups to aldehydes, cycloadditions and others. Group: Heterocyclic Organic Compound. Alternative Names: 328123-04-2;(4R,5R)-(-)-2,2-DIMETHYL-ALPHA,ALPHA,ALPHA',ALPHA'-TETRAPHENYL-1,3-DIOXOLANE-4,5-DIMETHANOLATO[1,2-BIS(DIMETHOXY)ETHANE]TITANIUM (IV) DICHLORIDE; MFCD04973054; SC10833; Tetraphenyl-TADDOL-DME-titaniumdichloride; 123D042; (4R, 5R)-(-)-2, 2-Di-Me-tetraphenyl-1, 3-dioxolane-4, 5-dimethanolato[1, 2-bis(diMeO)ethane]Ti(IV) dichloride CH3CN adduct;(4R,5R)-(-)-2,2-Dimethyl-alpha,alpha,alpha',alpha'-tetraphenyl-1,3-dioxolane-4,5-dimethanolato(1,2-bis(dimethoxy)ethane)titanium(IV) dichloride;(4R,5R)-(-)-2,2-DIMETHYL-ALPHA,ALPHA,ALPHA',ALPHA'-TETRAPHENYL-1,3-DIOXOLANE-4,5-DIMETHANOLATO[1,2-BIS(DIMETHOXY)ETHANE]TITANIUM(IV) DICHLORIDE ACETONITRILE ADDUCT. CAS No. 328123-04-2. Molecular formula: C37H45Cl2NO6Ti. Mole weight: 718.535g/mol. IUPAC Name: acetonitrile;cyclohexa-1,3-dien-1-yl-[(4R,5R)-5-[hydroxy(diphenyl)methyl]-2,2-dimethyl-1,3-dioxolan-4-yl]-phenylmethanol;dichlorotitanium;1,2-dimethoxyethane. Rotatable Bond Count: 7. Exact Mass: 717.21g/mol. SMILES: CC#N. CC1 (OC (C (O1)C (C2=CC=CC=C2) (C3=CC=CC=C3)O)C (C4=CC=CCC4) (C5=CC=CC=C5)O)C. COCCOC. Cl[Ti]Cl. InChI: InChI=1S/C31H32O4. C4H10O2. C2H3N. 2ClH. Ti/c1-29(2)34-27(30(32, 23-15-7-3-8-16-23)24-17-9-4-10-18-24)28(35-29)31(33, 25-19-11-5-12-20-25)26-21-13-6-14-22-26; 1-5-3-4-6-2; 1-2-3; ; ; /h3-13, 15-21, 27-28, 32-33H, 14, 22H2, 1-2H3; 3-4H2, 1-2H3; 1H3; 2*1H; /q; ; ; ; ; +2/p-2/t27-, 28-, 31 ;;;;;/m1../s1. InChIKey: YTJMLZYQYKUFOH-IWLCBTADSA-L. H-Bond Donor: 2. H-Bond Acceptor: 7. Monoisotopic Mass: 717.21g/mol. | |
5-Methyl-5-allyloxycarbonyl-1,3-dioxan-2-one Quick inquiry Where to buy Suppliers range | 5-Methyl-5-allyloxycarbonyl-1,3-dioxan-2-one. Uses: This monomer contains a pendant allyl group for thiol-ene click chemistry; to be copolymerized with lactides or glycolides for biodegradable polymers containing pendant functional groups. Group: CHO Containing Functional Groups. Alternative Names: Allyl 5-methyl-2-oxo-1,3-dioxane-5-carboxylate, Allyl functionalized carbonate monomer, 5-Methyl-2-oxo-1,3-dioxane-5-carboxylic acid, 2-propen-1-yl ester, MAC. CAS No. 532424-75-2. Molecular Weight: 200.19. SMILES: O=C1OCC(C(OCC=C)=O)(C)CO1. Flash Point: 97%. | |
Acarbose-N-allyl Formate Tridecaacetate Quick inquiry Where to buy Suppliers range | Acarbose-N-allyl Formate Tridecaacetate is an intermediate formed in the synthesis of α-D-Glucosyl Acarbose Impurity, a homolog of Acarbose for use in the treatment of chronic diseases such as inflammatory (including allergic) diseases, metastatic cancers and infection by pathogenic agents including bacteria, viruses or parasites. Synonyms: (3R,4S,5R,6R)-6-(Acetoxymethyl)-5-(((2R,3R,4S,5R,6R)-3,4-diacetoxy-6-(acetoxymethyl)-5-(((2R,3R,4S,5R,6R)-3,4-diacetoxy-5-(((allyloxy)carbonyl)((1S,4S,5S,6S)-4,5,6-triacetoxy-3-(acetoxymethyl)cyclohex-2-en-1-yl)amino)-6-methyltetrahydro-2H-pyran-2-yl)oxy)tetrahydro-2H-pyran-2-yl)oxy)tetrahydro-2H-pyran-2,3,4-triyl triacetate. Molecular formula: C55H73NO33. Mole weight: 1276.16. | |
Allyl Ester of Atorvastatin Cyclic (Fluorophenyl) Impurity Quick inquiry Where to buy Suppliers range | Intermediate in the preparation of Atorvastatin degradation products. Group: Biochemicals. Alternative Names: 1 β-(4-Fluorophenyl)hexahydro- β , 7-dihydroxy-7- (1-methylethyl)-1α -phenyl-7α -[ (phenylamino)carbonyl]-3H-oxireno[3, 4]pyrrolo[2, 1-b][1, 3]oxazine-3-butanoic Acid Allyl Ester; Allyl-ATV-cycloFP. Grades: Highly Purified. CAS No. 1316643-57-8. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
Atorvastatin Allyl Ester Quick inquiry Where to buy Suppliers range | Atorvastatin derivative. Group: Biochemicals. Alternative Names: 2-(4-Fluorophenyl)- β , δ -dihydroxy-5- (1-methylethyl)-3-phenyl-4-[ (phenylamino)carbonyl]-1H-pyrrole-1-heptanoic Acid 2-Propenyl Ester; ( βR,δR)-2-(4-Fluorophenyl)- β , δ -dihydroxy-5- (1-methylethyl)-3-phenyl-4-[ (phenylamino)carbonyl]-1H-pyrrole-1-heptanoic Acid 2-Propen-1-yl Ester. Grades: Highly Purified. CAS No. 915092-85-2. Pack Sizes: 25mg. US Biological Life Sciences. | Worldwide |
Atorvastatin Lactam Allyl Ester Quick inquiry Where to buy Suppliers range | Intermediate in the preparation of Atorvastatin degradation products. Group: Biochemicals. Alternative Names: ( βR,δR)-5-(4-Fluorophenyl)-2,3-dihydro- β , δ -dihydroxy-3- (1-methylethyl)-2-oxo-4-phenyl-3-[ (phenylamino)carbonyl]-1H-pyrrole-1-heptanoic Acid Allyl Ester. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
Boc-3,4-dichloro-D-phenylalanine Quick inquiry Where to buy Suppliers range | Boc-3,4-dichloro-D-phenylalanine is used to prepare fluorinated β-aminoacyl 1,2,4-triazolo[4,3-a]piperazine amides as dipeptidyl peptidase IV inhibitors and antidiabetic agents. It is also used in the synthesis of N-[(R,R)-(E)-1-(3,4-dichlorobenzyl)-3-(2-oxoazepan-3-yl)carbamoyl]allyl-N-methyl-3,5-bis(trifluoromethyl)benzamide as a potent and orally active dual neurokinin NK1/NK2 receptor antagonist. Synonyms: Boc-D-Phe(3,4-DiCl)-OH; Boc-D-Phe(3,4-Cl2)-OH; (R)-Boc-2-amino-3-(3,4-dichlorophenyl)propionic acid; Boc-D-Phe(3,4-Cl2)-OH; (R)-2-((tert-Butoxycarbonyl)amino)-3-(3,4-dichlorophenyl)propanoic acid; D-Phenylalanine, 3,4-dichloro-N-[(1,1-dimethylethoxy)carbonyl]-; Boc-D-3,4-Dichlorophenylalanine; AK162594; N-BOC-3,4-DICHLORO-D-PHENYLALANINE. Grades: ≥ 98% (HPLC). CAS No. 114873-13-1. Molecular formula: C14H17Cl2NO4. Mole weight: 334.20. | |
Chloro[1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene]copper(I) Quick inquiry Where to buy Suppliers range | Chloro[1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene]copper(I). Uses: Catalyst for the aziridination of olefins. Mild catalyst, superior to CuCl, in the methylenetriphenylphosphorane methyleneation of aldehydes and ketones. Copper(I) catalyzed alkylation of aryl and alkenylsilanes. Copper-catalyzed formal methylative and hydrogenative carboxylation of alkynes with carbon dioxide. Regioselective copper-catalyzed carboxylation of allylboronates with carbon dioxide. Carboxylation of organoboronic esters with potassium methyl carbonate under copper catalysis. Catalytic anti-Markovnikov hydrobromination of alkynes. Copper-catalyzed borylative cross-coupling of allenes and imines. Group: Heterocyclic Organic Compound. Grades: >98.0%(T). CAS No. 578743-87-0. Molecular formula: C27H36ClCuN2. Mole weight: 487.60. IUPAC Name: Chloro[1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene]copper(I). Exact Mass: 486.18600. Melting Point: >300 . | |
N-β-(t-Butoxycarbonyl)-β-allyl-D-β-homoglycine Quick inquiry Where to buy Suppliers range | Synonyms: Boc-D-Gly(Allyl)-(C#CH2)OH; (R)-3-[(t-Butoxycarbonyl)amino]-5-hexenoic acid; (3R)-3-[(2-methylpropan-2-yl)oxycarbonylamino]hex-5-enoic acid; (3R)-3-[[(1,1-Dimethylethoxy)carbonyl]amino]-5-hexenoicacid; 5-Hexenoicacid,3-[[(1,1-dimethylethoxy)carbonyl]amino]-,(3R); (3R)-3-[(tert-butoxycarbonyl)amino]hex-5-enoic acid; Boc-D-β-homoallylglycine; Boc-D-β-HomoGly(allyl)-OH; Boc-(R)-3-amino-5-hexenoic acid. Grades: ≥ 98% (HPLC). CAS No. 269726-94-5. Molecular formula: C11H19NO4. Mole weight: 229.27. | |
N-t-Boc-L-serine Allyl Ester Quick inquiry Where to buy Suppliers range | N-t-Boc-L-serine Allyl Ester, 143966-57-8, prop-2-enyl (2S)-3-hydroxy-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoate, Allyl (tert-butoxycarbonyl)-L-serinate, L-Serine, N-[(1,1-dimethylethoxy)carbonyl]-, 2-propen-1-yl ester, SCHEMBL1701200, DTXSID10463440, AKOS030241087, N-tert-butoxycarbonyl-L-serine allyl ester, N-(tert-butoxycarbonyl)-L-serine allyl ester, J-007888, (2S)-2-(tert-Butyloxycarbonylamino)-3-hydroxypropionic acid allyl ester, prop-2-en-1-yl (2S)-2-{[(tert-butoxy)carbonyl]amino}-3-hydroxypropanoate. | |
(R,R)-(-)-2,3-Bis(t-butylmethylphosphino)quinoxaline, min. 98% (R,R)-QuinoxP* Quick inquiry Where to buy Suppliers range | (R,R)-(-)-2,3-Bis(t-butylmethylphosphino)quinoxaline, min. 98% (R,R)-QuinoxP*. Uses: Ligand for the rhodium-catalyzed, asymmetric hydrogenation of dehydroamino acid esters and α-enamides. Ligand for the rhodium-catalyzed, asymmetric 1,4-addition of arylboronic acids to α,β-unsaturated carbonyl compounds. Ligand for the rhodium-catalyzed, asymmetric alkylative ring opening reaction Ligand for the palladium-catalyzed asymmetric allylic alkylation and amination of racemic substrates. Ligand for the ruthenium-catalyzed asymmetric hydrogenation of ketones. Ligand for the rhodium-catalyzed, asymmetric hydroacylation of 1,1-disubstituted alkenes with aldehydes. Ligand for the silver-catalyzed asymmetric nitroso aldol reaction. Cu-catalyzed enantioconvergent allyllic borylation. Cu-catalyzed enantioselective cyclopropylation. Group: Heterocyclic Organic Compound. Alternative Names: AK173366; 866081-62-1; (R,R)-(-)-2,3-Bis(tert-butylmethylphosphino)quinoxaline; (R,R)-QuinoxP; (R,R)-(-)-2,3-Bis(t-butylmethylphosphino)quinoxaline. CAS No. 866081-62-1. Molecular formula: C18H28N2P2. Mole weight: 334.384g/mol. IUPAC Name: (R)-tert-butyl-[3-[tert-butyl(methyl)phosphanyl]quinoxalin-2-yl]-methylphosphane. Rotatable Bond Count: 4. Exact Mass: 334.173g/mol. SMILES: CC (C) (C)P (C)C1=NC2=CC=CC=C2N=C1P (C)C (C) (C)C. InChI: InChI=1S/C18H28N2P2/c1-17(2,3)21(7)15-16(22(8)18(4,5)6)20-14-12-10-9-11-13(14)19-15/h9-12H,1-8H3/t21-,22-/m0/s1. InChIKey: DRZBLHZZDMCPGX-VXKWHMMOSA-N. H-Bond Acceptor: 2. Monoisotopic Mass: 334.173g/mol. | |
(S,S)-(+)-2,3-Bis(t-butylmethylphosphino)quinoxaline, min. 98% (S,S)-QuinoxP* Quick inquiry Where to buy Suppliers range | (S,S)-(+)-2,3-Bis(t-butylmethylphosphino)quinoxaline, min. 98% (S,S)-QuinoxP*. Uses: Ligand for the rhodium-catalyzed, asymmetric hydrogenation of dehydroamino acid esters and α-enamides. Ligand for the rhodium-catalyzed, asymmetric 1,4-addition of arylboronic acids to α,β-unsaturated carbonyl compounds. Ligand for the rhodium-catalyzed, asymmetric alkylative ring opening reaction Ligand for the palladium-catalyzed asymmetric allylic alkylation and amination of racemic substrates. Ligand for the ruthenium-catalyzed asymmetric hydrogenation of ketones. Ligand for the rhodium-catalyzed, asymmetric hydroacylation of 1,1-disubstituted alkenes with aldehydes. Ligand for the silver-catalyzed asymmetric nitroso aldol reaction. Alternative Names: (S, S)-(+)-2, 3-Bis(t-butylmethylphosphino)quinoxaline; 1107608-80-9; (S, S)-2, 3-Bis(tert-butylmethylphosphino)quinoxaline; (S, S)-QuinoxP*; SCHEMBL2559367; 2, 3-Bis[(S)-tert-butylmethylphosphino]quinoxaline; J-002473; (S, S)-(+)-2, 3-Bis(tert-butylmethylphosphino)quinoxaline. CAS No. 1107608-80-9. Molecular formula: C18H28N2P2. Mole weight: 334.384g/mol. IUPAC Name: (S)-tert-butyl-[3-[tert-butyl(methyl)phosphanyl]quinoxalin-2-yl]-methylphosphane. Rotatable Bond Count: 4. Exact Mass: 334.173g/mol. SMILES: CC (C) (C)P (C)C1=NC2=CC=CC=C2N=C1P (C)C (C) (C)C. InChI: InChI=1S/C18H28N2P2/c1-17(2,3)21(7)15-16(22(8)18(4,5)6)20-14-12-10-9-11-13(14)19-15/h9-12H,1-8H3/t21-,22-/m1/s1. InChIKey: DRZBLHZZDMCPGX-FGZHOGPDSA-N. H-Bond Acceptor: 2. Monoisotopic Mass: 334.173g/mol. | |
(S)-tert-Butyl 5-(((R)-1-(tert-Butoxy)-3-mercapto-1-oxopropan-2-yl)amino)-2-((tert-butoxycarbonyl)amino)-5-oxopentanoate Quick inquiry Where to buy Suppliers range | (S)-tert-Butyl 5-(((R)-1-(tert-Butoxy)-3-mercapto-1-oxopropan-2-yl)amino)-2-((tert-butoxycarbonyl)amino)-5-oxopentanoate is an intermediate in the synthesis of L-γ-Glutamyl-(S)-Allyl-Cysteine, which is an extract from garlic used in the production of inflammatory mediators. Synonyms: 2-Methyl-2-propanyl (2S)-2-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)-5-({(2R)-1-[(2-methyl-2-propanyl)oxy]-1-oxo-3-sulfanyl-2-propanyl}amino)-5-oxopentanoate. CAS No. 2112809-06-8. Molecular formula: C21H38N2O7S. Mole weight: 462.60. |