99865-15-3

Basic information

• Product Name: 2-(1-Phenylethyl)acrylic acid
• Synonyms: 2-(1-Phenylethyl)acrylic acid
• CAS NO: 99865-15-3
• Molecular Weight: 176.215
• Mol File: 99865-15-3.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 2-(1-Phenylethyl)acrylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(1-Phenylethyl)acrylic acid(99865-15-3)
• EPA Substance Registry System: 2-(1-Phenylethyl)acrylic acid(99865-15-3)

Safety Data

• Hazardous Substances Data: 99865-15-3(Hazardous Substances Data)

Upstream product

• 41103-90-6 (1-phenyl-ethyl)-malonic acid 
• 109-89-7 diethylamine 
• 847654-05-1 (+/-)-methyl 2-methylene-3-phenylbutanoate 
• 585-71-7 (1-bromoethyl)benzne 
• 81699-67-4 ethyl 2-methylene-3-phenylbutanoate 
• 6622-76-0 methyl (E)-2-methyl-2-butenoate 

Downstream Products

• 150881-62-2 2-<(acetylthio)methyl>-3-phenylbutanoic acid 
• 150881-36-0 (S)-2-(2-Acetylsulfanylmethyl-3-phenyl-butyrylamino)-propionic acid benzyl ester 
• 155895-89-9 (S)-2-((2R,3R)-2-Mercaptomethyl-3-phenyl-butyrylamino)-propionic acid 
• 155895-89-9 (S)-2-((2R,3S)-2-Mercaptomethyl-3-phenyl-butyrylamino)-propionic acid 
• 155895-89-9 RB 105 
• 155895-89-9 (S)-2-((2S,3S)-2-Mercaptomethyl-3-phenyl-butyrylamino)-propionic acid 
• 155895-89-9 (S)-2-(2-Mercaptomethyl-3-phenyl-butyrylamino)-propionic acid 
• 150881-70-2 (2R,3R)-2-<(acetylthio)methyl>-3-phenylbutanoic acid 
• 150881-68-8 (2R,3S)-2-<(acetylthio)methyl>-3-phenylbutanoic acid 
• 150881-69-9 (2S,3R)-2-<(acetylthio)methyl>-3-phenylbutanoic acid 
• 155779-75-2 (2S,3S)-2-<(acetylthio)methyl>-3-phenylbutanoic acid 

Relevant articles and documents

Mapping the mechanism of nickel-ferrophite catalysed methylation of baylis-hillman-derived SN2′ electrophiles

Enantioselective Ni-catalysed methylation of Baylis-Hillman-derived allylic electrophiles in the presence of ferrophite ligands has been investigated computationally and experimentally. The sense and degree of enantioselectivity attained is independent of both the leaving group and the isomeric structure of the initial allylic halide. DFT studies support the selective formation of a limited number of energetically favoured anti and syn π-allyl intermediates. The observed regio- and enantioselectivity can be rationalised based on the energetics of these structures.

Process for the synthesis of α-substituted acrylic acids and their application

Process for the synthesis of a-substituted acrylic acids and their application. Process for the synthesis of a-substituted acrylic acids of general formula (I) and their application to the synthesis of N- (mercaptoacyl) aminoacid derivatives of formula (II). STR1

New dual inhibitors of neutral endopeptidase and angiotensin-converting enzyme: Rational design, bioavailability, and pharmacological responses in experimental hypertension

In the treatment of cardiovascular diseases, it could be of therapeutic interest to associate the hypotensive effects resulting from the inhibition of angiotensin II formation, ensured by endothelial angiotensin-converting enzyme (ACE), with the diuretic