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a-Amyl cinnamic aldehyde diethyl acetal. Uses: Designed for use in research and industrial production. Additional or Alternative Names: (2-(diethoxymethyl)-1-heptenyl)-benzen;(2-(diethoxymethyl)-1-heptenyl)benzene;[2-(diethoxymethyl)-1-heptenyl]-benzen;[2-(diethoxymethyl)-1-heptenyl]-Benzene;1,1-diethoxy-2-(phenylmethylene)-heptan;1,1-diethoxy-2-(phenylmethylene)heptane;1,1-diethoxy-2-am. Product Category: Heterocyclic Organic Compound. CAS No. 60763-41-9. Molecular formula: C18H28O2. Mole weight: 276.41. Product ID: ACM60763419. Alfa Chemistry ISO 9001:2015 Certified. Categories: D3K7R9235H.
Alpha Methyl Cinnamic Aldehyde
Alpha Methyl Cinnamic Aldehyde. CAS No. 101-39-3. Molecular formula: C10H10O.
1-Hydroxy-3-phenyl-1,3-propanedisulfonic acid disodium salt
1-Hydroxy-3-phenyl-1,3-propanedisulfonic acid disodium salt. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 1-Hydroxy-3-phenyl-1,3-propanedisulfonic acid disodium salt;Cinnamic aldehyde disodium disulfite. Product Category: Heterocyclic Organic Compound. CAS No. 105391-35-3. Product ID: ACM105391353. Alfa Chemistry ISO 9001:2015 Certified.
Used in organic synthesis especially in Perkin synthesis; formation of unsaturated cinnamic-type acids by the condensation of aromatic aldehydes with fatty acids. Group: Biochemicals. Alternative Names: Acetic acid cesium salt. Grades: Reagent Grade. CAS No. 3396-11-0. Pack Sizes: 100g, 250g, 1Kg. Molecular Formula:?C2H3CsO2. US Biological Life Sciences.
Worldwide
Cinnamaldehyde
Cinnamaldehyde, a major component of cinnamon, induces the generation of reactive oxygen species and exerts vasodilator and anticancer effects. Uses: Antipyretic. Synonyms: 3-Phenyl-2-propenal; 3-Phenyl-2-propen-1-al; 3-Phenyl-2-propenaldehyde; 3-Phenyl-2-propene-1-al; 3-Phenylacrolein; 3-Phenylacrylaldehyde; 3-Phenylpropenal; Abion CA; Benzylideneacetaldehyde; Cassia aldehyde; Cinnacure; Cinnamal; Cinnamic aldehyde; Cinnamite; Cinnamyl aldehyde; NSC 16935; NSC 40346; Phenylacrolein; XC 800; Zimtaldehyde; β-Phenylacrolein. Grades: >98%. CAS No. 104-55-2. Molecular formula: C9H8O. Mole weight: 132.16.
Cinnamaldehyde
Cinnamaldehyde. Group: Biochemicals. Alternative Names: Cinnamic aldehyde; 3-Phenyl-2-propenal. Grades: Highly Purified. CAS No. 104-55-2. Pack Sizes: 1kg, 2kg, 5kg, 10kg, 25kg. Molecular Formula: C6H5CH=CHCHO. US Biological Life Sciences.
Shows highest activity with 1-nitrocyclohexene but also has significant activity with 2-methylpentenal and trans-cinnamaldehyde. Involved in the detoxication of α,β-unsaturated aldehydes and ketones. Has very low activity with NAD as reductant (cf. EC 1.3.1.74, 2-alkenal reductase [NAD(P)+]). Group: Enzymes. Synonyms: NADPH-dependent alkenal/one oxidoreductase; NADPH:2-alkenal α,β-hydrogenase. Enzyme Commission Number: EC 1.3.1.102. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1274; 2-alkenal reductase (NADP+); EC 1.3.1.102; NADPH-dependent alkenal/one oxidoreductase; NADPH:2-alkenal α,β-hydrogenase. Cat No: EXWM-1274.
aryl-alcohol dehydrogenase (NADP+)
Also acts on some aliphatic aldehydes, but cinnamaldehyde was the best substrate found. Group: Enzymes. Synonyms: aryl alcohol dehydrogenase (nicotinamide adenine dinucleotide phosphate); coniferyl alcohol dehydrogenase; NADPH-linked benzaldehyde reductase; aryl-alcohol dehydrogenase (NADP). Enzyme Commission Number: EC 1.1.1.91. CAS No. 37250-27-4. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0375; aryl-alcohol dehydrogenase (NADP+); EC 1.1.1.91; 37250-27-4; aryl alcohol dehydrogenase (nicotinamide adenine dinucleotide phosphate); coniferyl alcohol dehydrogenase; NADPH-linked benzaldehyde reductase; aryl-alcohol dehydrogenase (NADP). Cat No: EXWM-0375.
Palladium(II)(π-cinnamyl) Chloride Dimer
Palladium(II)(π-cinnamyl) Chloride Dimer. Uses: Precursor for the preparation of a palladium catalyst used in the carbonylative arylation of ketones, yielding vinylbenzoate compounds. precursor for the preparation of a palladium catalyst used in the buchwald-hartwig amination of (hetero)aryl chlorides. precursor for the preparation of a palladium catalyst used in the arylative dearomatization of phenols. versatile palladium precursor for the preparation of palladium catalysts used in the cross-coupling of aryl chlorides and amines , conversion of aryl triflates to aryl fluorides , and the α-arylation of aldehydes. Additional or Alternative Names: 12131-44-1;Palladium(|Eth-cinnamyl) chloride dimer;AK136149;PALLADIUM(PI-CINNAMYL) CHLORIDE DIMER;Di- -chlorobis[(1,2,3- )-1-phenyl-2-propen-1-yl]dipalladium;Di-|I-chlorobis[(1,2,3-|C)-1-phenyl-2-propen-1-yl]dipalladium;Di-|I-chlorobis[(1,2,3-|C)-1-phenyl-2-propenyl]dipalladium(II);Di-mu-chlorobis[(1,2,3-eta)-1-phenyl-2-propen-1-yl]dipalladium. Product Category: Palladium series catalysts. CAS No. 12131-44-1. Molecular formula: C18H18Cl2Pd2. Mole weight: 518.082g/mol. IUPACName: palladium(2+);prop-2-enylbenzene;dichloride. Canonical SMILES: C=C[CH-]C1=CC=CC=C1.C=C[CH-]C1=CC=CC=C1.[Cl-].[Cl-].[Pd+2].[Pd+2]. Product ID: ACM12131441. Alfa Chemistry ISO 9001:2015 Certified.
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