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| Product | Description | |
|---|---|---|
| Dibenzylideneacetone | 25g Pack Size. Group: Building Blocks, Organics. Formula: C17H14O. CAS No. 35225-79-7. Prepack ID 47854783-25g. Molecular Weight 234.29. See USA prepack pricing. |  |
| Dibenzylideneacetone | Dibenzylideneacetone (Dibenzalacetone) is a potent inhibitor of chitinase with an IC 50 value of 13.10 μM. The MIC value of Dibenzylideneacetone against Botrytis cinerea is 32 μg/mL, and the EC 50 values for inhibiting mycelium growth and spore germination are 16.29 and 14.64 μg/mL, respectively. Dibenzylideneacetone can be used in research on fruit and vegetable preservatives [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Dibenzalacetone. CAS No. 538-58-9. Pack Sizes: 10 mM * 1 mL; 5 g. Product ID: HY-75828. |  |
| Dibenzylideneacetone (DBA) | Dibenzylideneacetone (DBA). Group: Biochemicals. Grades: Highly Purified. CAS No. 538-58-9. Pack Sizes: 250g, 500g, 1kg, 2kg, 5kg. Molecular Formula: C17H14O. US Biological Life Sciences. |  Worldwide |
| Bis (dibenzylideneacetone) palladium | Bis (dibenzylideneacetone) palladium is a compound used as a component of a potentiometric membrane sensor to selectively determine the presence of thiocyanate in the urine of cigarette smokers. Bis (dibenzylideneacetone) palladium is also used as one of the homogeneous catalysts in the synthesis of Tricyclopentadiene from Dicyclopentadiene (D439350). Group: Biochemicals. Grades: Highly Purified. CAS No. 32005-36-0. Pack Sizes: 1g, 2.5g. Molecular Formula: C34H28O2Pd. US Biological Life Sciences. | Worldwide |
| Bis(dibenzylideneacetone)palladium | Bis(dibenzylideneacetone)palladium is a biochemical reagent that can be used as a biological material or organic compound for life science related research. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 32005-36-0. Pack Sizes: 500 mg; 1 g. Product ID: HY-W001137. | |
| Bis (dibenzylideneacetone) palladium (0) | Bis (dibenzylideneacetone) palladium (0) . Group: Biochemicals. Alternative Names: Palladium(0) Bis (dibenzylideneacetone) . Grades: Highly Purified. CAS No. 32005-36-0. Pack Sizes: 1g, 2g, 5g, 10g, 25g. Molecular Formula: C34H28O2Pd. US Biological Life Sciences. | Worldwide |
| Bis (dibenzylideneacetone)palladium (0) | Bis (dibenzylideneacetone)palladium (0). Uses: Palladium-catalyzed acylation of unsaturated halides by anions of enol ethers. asymmmetric allylation reactions. intramolecular reactions with alkenes. carbonylation reactions. cross coupling reactions. Group: Salt. Alternative Names: CB-706; MFCD00051942; Bis (dibenzylideneacetone)palladium (0); (1E,4E)-1,5-diphenylpenta-1,4-dien-3-one,palladium; GC10019; RW2139; bis(dibenzylidene-acetone)palladium; bis (dibenzylideneacetone)palladium; PubChem14428; J-400823. CAS No. 32005-36-0. Product ID: (1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladium. Molecular formula: 575.016g/mol. Mole weight: C34H28O2Pd. C1=CC=C(C=C1)C=CC(=O)C=CC2=CC=CC=C2. C1=CC=C(C=C1)C=CC(=O)C=CC2=CC=CC=C2. [Pd]. InChI=1S/2C17H14O. Pd/c2*18-17 (13-11-15-7-3-1-4-8-15) 14-12-16-9-5-2-6-10-16; /h2*1-14H; /b2*13-11+, 14-12+;. UKSZBOKPHAQOMP-SVLSSHOZSA-N. |  |
| Bis (dibenzylideneacetone)palladium (0) | Palladium-catalyzed acylation of unsaturated halides by anions of enol ethers. Asymmmetric Allylation reactions. Intramolecular reactions with alkenes. Carbonylation reactions. Cross Coupling reactions. Group: Palladium series catalysts. Alternative Names: CB-706; MFCD00051942; Bis (dibenzylideneacetone)palladium (0); (1E,4E)-1,5-diphenylpenta-1,4-dien-3-one,palladium; GC10019; RW2139; bis(dibenzylidene-acetone)palladium; bis (dibenzylideneacetone)palladium; PubChem14428; J-400823. CAS No. 32005-36-0. Molecular formula: C34H28O2Pd. Mole weight: 575.016g/mol. IUPACName: (1E,4E)-1,5-diphenylpenta-1,4-dien-3-one;palladium. Canonical SMILES: C1=CC=C(C=C1)C=CC(=O)C=CC2=CC=CC=C2. C1=CC=C(C=C1)C=CC(=O)C=CC2=CC=CC=C2. [Pd]. ECNumber: 608-691-6. Catalog: ACM32005360. |  |
| Bis (dibenzylideneacetone) palladium (0) ≥97% (18.0-18.6% Palladium content) | Bis (dibenzylideneacetone) palladium (0) ≥97% (18.0-18.6% Palladium content). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g, 100g. US Biological Life Sciences. | Worldwide |
| Pd2dba3 (Tris(dibenzylideneacetone)dipalladium(0)) | Pd2dba3 (Tris(dibenzylideneacetone)dipalladium(0)). CAS No: 51364-51-3 |  Sarchem Laboratories New Jersey NJ |
| Trans,Trans-Dibenzylideneacetone | Trans,Trans-Dibenzylideneacetone. CAS No: 35225-79-7 | Sarchem Laboratories New Jersey NJ |
| trans,trans-Dibenzylideneacetone, 99% | Reactant involved in: ;Nazarov-like cyclization1 ;Transfer hydrogenation2 ;Lewis acid mediated condensation3 ;Hetero-Diels-Alder reactions4 ;Asymmetric 1,4-addition reactions5 ;Michael addition reactions6. Group: Heterocyclic organic compound. Alternative Names: RTC-070646; RP13462; cid_640180; AK-77431; AJ-26416; Dibenzalacetone; AKOS 213-33; CHM0032447; trans,trans-1,5-Diphenylpenta-1,4-dien-3-one; CHEMBL17201. CAS No. 35225-79-7. Molecular formula: C17H14O. Mole weight: 234.298g/mol. IUPACName: (1E,4E)-1,5-diphenylpenta-1,4-dien-3-one. Canonical SMILES: C1=CC=C(C=C1)C=CC(=O)C=CC2=CC=CC=C2. ECNumber: 208-697-5. Catalog: ACM35225797. | |
| Tris (dibenzylideneacetone)dipalladium (0) | Amination→Buchwald-Hartwig Aminaton; Carbonylation; Cross Coupling Reactions with Arenes→Mizoroki Heck Coupling Reaction; Cross Coupling Reactions with Arenes→Stille Reaction; Cross Coupling Reactions with Arenes→Suzuki-Miyaura Coupling Reaction; Oxidation; Reduction. Group: Palladium series catalysts. Alternative Names: Bis[tris (dibenzylideneacetone)palladium (0)]. CAS No. 51364-51-3. Molecular formula: C51H42O3Pd2. Mole weight: 915.73. Appearance: Purple black crystalline powder. Purity: 0.98. IUPACName: (1E,4E)-1,5-diphenylpenta-1,4-dien-3-one;palladium. Canonical SMILES: C1=CC=C(C=C1)C=CC(=O)C=CC2=CC=CC=C2. C1=CC=C(C=C1)C=CC(=O)C=CC2=CC=CC=C2. C1=CC=C(C=C1)C=CC(=O)C=CC2=CC=CC=C2. [Pd]. [Pd]. ECNumber: 610-654-4. Catalog: ACM51364513-2. | |
| Tris (dibenzylideneacetone)dipalladium (0) | Tris (dibenzylideneacetone)dipalladium (0). Uses: Amination→buchwald-hartwig aminaton; carbonylation; cross coupling reactions with arenes→mizoroki heck coupling reaction; cross coupling reactions with arenes→stille reaction; cross coupling reactions with arenes→suzuki-miyaura coupling reaction; oxidation; reduction. Group: Salt. Alternative Names: Bis[tris (dibenzylideneacetone)palladium (0)]. CAS No. 51364-51-3. Product ID: (1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladium. Molecular formula: 915.73. Mole weight: C51H42O3Pd2. C1=CC=C(C=C1)C=CC(=O)C=CC2=CC=CC=C2. C1=CC=C(C=C1)C=CC(=O)C=CC2=CC=CC=C2. C1=CC=C(C=C1)C=CC(=O)C=CC2=CC=CC=C2. [Pd]. [Pd]. InChI=1S/3C17H14O. 2Pd/c3*18-17 (13-11-15-7-3-1-4-8-15) 14-12-16-9-5-2-6-10-16; /h3*1-14H; /b3*13-11+, 14-12+. CYPYTURSJDMMMP-WVCUSYJESA-N. 98%. | |
| Tris (dibenzylideneacetone) dipalladium (0) 18.5-23. | Tris (dibenzylideneacetone) dipalladium (0) 18.5-23. Group: Biochemicals. Grades: Highly Purified. CAS No. 51364-51-3. Pack Sizes: 1g, 2g, 5g, 10g, 25g. Molecular Formula: 3CI7H14O·Pd. US Biological Life Sciences. | Worldwide |
| Tris (dibenzylideneacetone) dipalladium (0), 19-23% (Palladium) | Tris (dibenzylideneacetone) dipalladium (0), 19-23% (Palladium). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g, 100g. US Biological Life Sciences. | Worldwide |
| Tris (dibenzylideneacetone) dipalladium (0)-chloroform adduct | Tris (dibenzylideneacetone) dipalladium (0)-chloroform adduct. Group: Biochemicals. Alternative Names: Dipalladium ()tris (dibenzylideneacetone)-chloroform adduct. Grades: Highly Purified. CAS No. 52522-40-4. Pack Sizes: 1g, 2g, 5g, 10g, 25g. US Biological Life Sciences. | Worldwide |
| Tris (dibenzylideneacetone)dipalladium (0) chloroform adduct | Tris (dibenzylideneacetone)dipalladium (0) chloroform adduct. Uses: Used for pd-catalyzed asymmetric arylation, vinylation, and allenylation of tert-cyclobutanols via enantioselective c-c bond cleavage. used for synthesis of chiral chromans through the pd-catalyzed asymmetric allylic alkylation (aaa). catalyst for double n-arylation of primary amines to synthesize multisubstituted carbazoles from 2,2'biphenylylene ditriflates. paladium catalyst for regioand enanti. Group: Salt. Alternative Names: Tris(dibenylideneacetone)dipalladium-chloroform; tris- (dibenzylideneacetone)-dipalladium (o)-chloroform adduct; tris (dibenzylideneacetone)-dipalladium (0) chloroform adduct; DIPALLADIUM (0)TRIS (DIBENZYLIDENEACETONE)-CHLOROFORM ADDUCT; tris(dibenzylideneacetone) dipalladium(0)chloroform adduct; GC10022; I14-10041; tris(dibenzylideneacetone) dipalladium chloroform; tris (dibenzylideneacetone)dipa. CAS No. 52522-40-4. Product ID: chloroform; (1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladium. Molecular formula: 1035.103g/mol. Mole weight: C52H43Cl3O3Pd2. C1=CC=C(C=C1)C=CC(=O)C=CC2=CC=CC=C2. C1=CC=C(C=C1)C=CC(=O)C=CC2=CC=CC=C2. C1=CC=C(C=C1)C=CC(=O)C=CC2=CC=CC=C2. C(Cl)(Cl)Cl. [Pd]. [Pd]. InChI=1S/3C17H14O. CHCl3. 2Pd/c3*18-17 (13-11-15-7-3-1-4-8-15) 14-12-16-9-5-2-6-10-16; 2-1 (3) 4; ; /h3*1-14H; 1H; ; /b3*13-11+, 14-12+; ; ;. LNAMMBFJMYMQTO-FNEBRGMMSA-N. | |
| Tris (dibenzylideneacetone)dipalladium (0) chloroform adduct | Used for Pd-catalyzed asymmetric arylation, vinylation, and Allenylation of tert-cyclobutanols via enantioselective C-C Bond cleavage. Used for synthesis of chiral chromans through the Pd-catalyzed asymmetric allylic alkylation (AAA). Catalyst for double N-arylation of primary amines to synthesize multisubstituted carbazoles from 2,2'biphenylylene ditriflates. Paladium catalyst for regioand enantioselective allylic alkylation of ketones through allyl enol carbonates. Used for Pd-catalyzed enantioselective C-3 allylation of 3-substituted-1H-indoles using trialkylboranes. Used for enantioselective construction of spirocyclic oxindolic cyclopentanes by Pd-catalyzed trimethylenemethane- [3+2]-cycloaddition. Used for Pd-catalyzed insertion of α-diazoesters into vinyl halides to generate α,β-unsaturated γ-amino Esters. Pd catalyst for decarboxylative asymmetric allylic alkylation of enol carbonates. Palladium catalyst for asymmetric addition of oxindoles and allenes. Catalyst for diastereoand enantioselective formal [3+2]-cycloaddition between substituted vinylcyclopropanes and electron-deficient olefins. Used for Pd-catalyzed asymmetric decarboxylative cycloaddition of vinylethylene carbonates with Michael sacceptors. Catalyst for enantioselective [6+4] cycloaddition of vinyl oxetanes with azadienes to access ten-membered heterocycles. Group: Palladium series | |
| Tris (dibenzylideneacetone) dipalladium (0)-chloroform adduct 98+% | Tris (dibenzylideneacetone) dipalladium (0)-chloroform adduct 98+%. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g. US Biological Life Sciences. | Worldwide |
| Tris (dibenzylideneacetone)platinum (0) | Liquid and Vapor Deposition Precursors. CAS No. 11072-92-7. Mole weight: 898. Appearance: Brown solid. Purity: 95%+. IUPACName: 1,5-Diphenylpenta-1,4-dien-3-one;platinum. Canonical SMILES: C1=CC=C(C=C1)C=CC(=O)C=CC2=CC=CC=C2. C1=CC=C(C=C1)C=CC(=O)C=CC2=CC=CC=C2. C1=CC=C(C=C1)C=CC(=O)C=CC2=CC=CC=C2. [Pt]. Catalog: ACM11072927. | |
| 1,5-Diphenylpenta-1,4-dien-3-one | 1,5-Diphenylpenta-1,4-dien-3-one. Group: Organic light-emitting diode (oled) materials. Alternative Names: Dibenzylideneacetone; 1,5-Diphenyl-3-pentadienone. CAS No. 538-58-9. Product ID: (1E,4E)-1,5-diphenylpenta-1,4-dien-3-one. Molecular formula: 234.29. Mole weight: C17H14O. C1=CC=C(C=C1)C=CC(=O)C=CC2=CC=CC=C2. WMKGGPCROCCUDY-PHEQNACWSA-N. InChI=1S / C17H14O / c18-17 (13-11-15-7-3-1-4-8-15) 14-12-16-9-5-2-6-10-16 / h1-14H / b13-11+, 14-12+. 98%. | |
| Tris DBA | Tris DBA has been found to be a N-myristoyltransferase-1 (NMT-1) inhibitor and could be used as a cyclization catalyst. Synonyms: Tris (dibenzylideneacetone)dipalladium; 1,4-Pentadien-3-one, 1,5-diphenyl-, palladium complex, (E,E)-; Palladium, tris[μ-[(1,2-η:4,5-η)-1,5-diphenyl-1,4-pentadien-3-one]]di-, (all-E)-; Tris[μ-[(1,2-η:4,5-η)-(1E,4E)-1,5-diphenyl-1,4-pentadien-3-one]]dipalladium; Pd2(DBA)3; Tris (dibenzylideneacetone)dipalladium; Tris(dibenzylideneacetonyl)bis-palladium; Tris[(1E,4E)-1,5-diphenyl-1,4-pentadien-3-one]dipalladium; Tris [dibenzylideneacetone]dipalladium (DBA palladium); tris[μ-[(1,2-η:4,5-η)-(1E,4E)-1,5-diphenyl-1,4-pentadien-3-one]]dipalladium [Pd2(dba)3]; Palladium, tris[μ-[(1,2-η:4,5-η)-(1E,4E)-1,5-diphenyl-1,4-pentadien-3-one]]di-. Grades: ≥95% by HPLC. CAS No. 51364-51-3. Molecular formula: C51H42O3Pd2. Mole weight: 915.73. |  |
| Tris(dibenzylideneacetonyl)bis-palladium | Tris(dibenzylideneacetonyl)bis-palladium is a catalyst that catalyzes the coupling reaction of N-methyl-2-pyrrolidinone (NMP) [1]. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 51364-51-3. Pack Sizes: 1 g; 5 g. Product ID: HY-W018864. | |
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