1914-59-6

Basic information

• Product Name: 3-Butenoic acid, 2-oxo-4-phenyl-, (E)-
• CAS NO: 1914-59-6
• Molecular Formula: C10H8O3
• Molecular Weight: 176.172
• Mol File: 1914-59-6.mol
• Article Data: 18

Chemical Properties

• CAS DataBase Reference: 3-Butenoic acid, 2-oxo-4-phenyl-, (E)-(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Butenoic acid, 2-oxo-4-phenyl-, (E)-(1914-59-6)
• EPA Substance Registry System: 3-Butenoic acid, 2-oxo-4-phenyl-, (E)-(1914-59-6)

Safety Data

• Hazardous Substances Data: 1914-59-6(Hazardous Substances Data)

Upstream product

• 140653-89-0 (E)-benzylideneglyoxylic acid potassium salt 
• 100-52-7 benzaldehyde 
• 113-24-6 sodium pyruvate 
• 1034123-64-2 (S)-4-hydroxy-2-oxo-4-phenylbutanoic acid 
• 99389-54-5 4-hydroxy-4-phenylbut-2-enoic acid 
• 112068-21-0 rac-(E)-2-hydroxy-4-phenyl-3-butenoic acid methyl ester 
• 107969-78-8 methyl benzylidenepyruvate 
• 600-22-6 pyruvic acid methyl ester 
• 140632-55-9 (R)-(E)-2-hydroxy-4-phenyl-3-butenoic acid 
• 127-17-3 2-oxo-propionic acid 
• 129029-61-4 2-hydroxy-4-phenylbut-3-enoic acid 
• 118806-93-2 2-oxo-4-phenylbut-3-enoic acid potassium salt 

Downstream Products

• 857778-91-7 4-phenyl-2-phenylimino-but-3-enoic acid 
• 140-10-3 (E)-3-phenylacrylic acid 
• 5464-35-7 2-hydroxyimino-4-phenyl-but-3-enoic acid 
• 79878-66-3 3-hydrazono-1t-phenyl-buten-⁽¹⁾-oic acid-⁽⁴⁾ 
• 108411-58-1 2-methoxyimino-4t-phenyl-but-3-enoic acid 
• 129029-61-4 2-hydroxy-4-phenylbut-3-enoic acid 
• 1012-05-1 D,L-homophenylalanine 
• 4263-93-8 2-hydroxy-4-phenylbutanoic acid 
• 861310-73-8 3,4-dibromo-2-oxo-4-phenyl-butyric acid 
• 524-42-5 1,2-naphthoquinone 
• 18124-61-3 5-methyl-2,6-dioxo-4,6-diphenyl-hexanoic acid 
• 122-97-4 3-Phenyl-1-propanol 
• 17451-20-6 (E)-ethyl-2-oxo-4-phenylbut-3-enoate 
• 959161-66-1 S-t-butyl 2-oxo-4-phenyl-but-3-enethioate 

Relevant articles and documents

Catalytic Three-Component Synthesis of Functionalized Naphtho[2,1-b]oxecines via a Double Bond Cleavage-Rearrangement Cascade

A new double annulation cascade involving a [2 + 2] cycloaddition-retroelectrocyclization (CA-RE) process was first reported, leading to the generation of unprecedented dibenzoannulated naphtho[2,1-b]oxecines with good to excellent yields and high stereos

Sbi00515, a Protein of Unknown Function from Streptomyces bingchenggensis, Highlights the Functional Versatility of the Acetoacetate Decarboxylase Scaffold

The acetoacetate decarboxylase-like superfamily (ADCSF) is a group of ～4000 enzymes that, until recently, was thought to be homogeneous in terms of the reaction catalyzed. Bioinformatic analysis shows that the ADCSF consists of up to seven families that d

Iridium/f-Amphox-Catalyzed Asymmetric Hydrogenation of Styrylglyoxylamides

We report an iridium-catalyzed asymmetric hydrogenation reaction for the preparation of chiral homophenylalanine derivatives. Catalyzed by an iridium/f-amphox complex, the asymmetric hydrogenation of styrylglyoxylamides was conducted smoothly with turnover numbers of up to 10,000 and up to 98% ee. This method was successfully applied in a synthesis of a fragment of benazepril, a drug used for the treatment of high blood pressure.

SUBSTITUTED DIHYDROPYRAZOLES AS SPHINGOSINE RECEPTOR MODULATORS

The present invention relates to substituted dihydropyrazoles, processes for preparing them, pharmaceutical compositions containing them and their use as pharmaceuticals as modulators of sphingosine-1-phosphate receptors.