62718-61-0

Basic information

• Product Name: (E)-3-(4-propylphenyl)acrylic acid
• Synonyms: (E)-3-(4-propylphenyl)acrylic acid
• CAS NO: 62718-61-0
• Molecular Formula: C₁₂H₁₄O₂
• Molecular Weight: 190.23836
• Mol File: 62718-61-0.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (E)-3-(4-propylphenyl)acrylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-3-(4-propylphenyl)acrylic acid(62718-61-0)
• EPA Substance Registry System: (E)-3-(4-propylphenyl)acrylic acid(62718-61-0)

Safety Data

• Hazardous Substances Data: 62718-61-0(Hazardous Substances Data)

Upstream product

• 103-65-1 phenylpropane 
• 1038997-26-0 (E)-n-butyl 3-(4-n-propylphenyl)acrylate 
• 141-82-2 malonic acid 
• 28785-06-0 4-n-propylbenzaldehyde 

Downstream Products

• 1038997-25-9 3-[(E)-3-(4-n-propylphenyl)-2-propenoyl]-2-thiazolidinethione 
• 1196690-91-1 C₁₂H₁₇NO₂ 
• 120680-79-7 3-Phenyl-2-[(E)-3-(4-propyl-phenyl)-acryloylamino]-propionic acid 
• 162752-13-8 3-(4-propylphenyl)propanoic acid 
• 120681-09-6 (E)-3-(4-Propyl-phenyl)-acryloyl chloride 
• 110683-42-6 (E)-3-(4-Propyl-phenyl)-N-[3-(1H-tetrazol-5-yl)-2,3-dihydro-benzo[1,4]dioxin-5-yl]-acrylamide 

Relevant articles and documents

Phenylalanine aminomutase-catalyzed addition of ammonia to substituted cinnamic acids: A route to enantiopure α- and β-amino acids

(Chemical Equation Presented) An approach is described for the synthesis of aromatic α- and β-amino acids that uses phenylalanine aminomutase to catalyze a highly enantioselective addition of ammonia to substituted cinnamic acids. The reaction has a broad scope and yields substituted α- and β-phenylalanines with excellent enantiomeric excess. The regioselectivity of the conversion is determined by substituents present at the aromatic ring. A box model for the enzyme active site is proposed, derived from the influence of the hydrophobicity of substituents on the enzyme affinity toward various substrates.

PHENYLALKYLCARBOXYLIC ACID DELIVERY AGENTS

The present invention provides phenylalkylcarboxylic acid compounds and compositions containing such compounds which facilitate the delivery of biologically active agents.

New potent antagonists of leukotrienes C4 and D4. 1. Synthesis and structure-activity relationships

(p-Amylcinnamoyl)anthranilic acid (3a) had moderate antagonist activities against LTD4-induced smooth muscle contraction on guinea pig ileum and LTC4-induced bronchoconstriction in anesthetized guinea pigs. Modifications were made in the hydrophobic part (cinnamoyl moiety) and the hydrophilic part (anthranilate moiety) of 3a. A series of 8-(benzoylamino)-2-tetrazol-5-yl-1,4-benzodioxans and 8-(benzoylamino)-2-tetrazol-5-yl-4-oxo-4H-1-benzopyrans were revealed to be potent antagonists of leukotrienes C4 and D4. Among both series, ONO-RS-347 (18k) and ONO-RS411 (19h) were the most potent and orally active antagonists, respectively. Structure-activity relationships are discussed.