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42287-94-5

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42287-94-5 Usage

General Description

3-(4-Cyanophenyl)propanoic acid is a chemical compound with the molecular formula C10H9NO2. It is a carboxylic acid derivative that contains both a phenyl and a cyanide group. 3-(4-CYANOPHENYL)PROPANOIC ACID is commonly used in the synthesis of various pharmaceuticals and is also a precursor for the production of numerous other organic compounds. It has been studied for its potential medicinal properties, particularly for its anti-inflammatory and analgesic effects. Additionally, 3-(4-Cyanophenyl)propanoic acid has also been used in the development of materials for various industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 42287-94-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,2,8 and 7 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 42287-94:
(7*4)+(6*2)+(5*2)+(4*8)+(3*7)+(2*9)+(1*4)=125
125 % 10 = 5
So 42287-94-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H9NO2/c11-7-9-3-1-8(2-4-9)5-6-10(12)13/h1-4H,5-6H2,(H,12,13)

42287-94-5 Well-known Company Product Price

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  • Alfa Aesar

  • (H34297)  3-(4-Cyanophenyl)propionic acid, 96%   

  • 42287-94-5

  • 250mg

  • 730.0CNY

  • Detail
  • Alfa Aesar

  • (H34297)  3-(4-Cyanophenyl)propionic acid, 96%   

  • 42287-94-5

  • 1g

  • 2022.0CNY

  • Detail
  • Alfa Aesar

  • (H34297)  3-(4-Cyanophenyl)propionic acid, 96%   

  • 42287-94-5

  • 5g

  • 3859.0CNY

  • Detail

42287-94-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-CYANOPHENYL)PROPANOIC ACID

1.2 Other means of identification

Product number -
Other names 4-CYANOBENZENEPROPANOIC ACID

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:42287-94-5 SDS

42287-94-5Relevant articles and documents

Photoredox Activation of Formate Salts: Hydrocarboxylation of Alkenes via Carboxyl Group Transfer

Huang, Yan,Hou, Jing,Zhan, Le-Wu,Zhang, Qian,Tang, Wan-Ying,Li, Bin-Dong

, p. 15004 - 15012 (2021/12/14)

A photoredox activation mode of formate salts for carboxylation was developed. Using a formate salt as the reductant, carbonyl source, and hydrogen atom transfer reagent, a wide range of alkenes can be converted into acid products via a carboxyl group tra

The polymorphism of porphyrin 2D assemblies at the liquid-graphite interface: The effect of a polar solvent additive and a flexible spacer on the face-on and edge-on type molecular arrangements

Adachi, Kenya,Hirose, Takashi,Matsuda, Kenji

supporting information, p. 8836 - 8839 (2019/08/01)

Self-assembly structures of 5,10,15,20-tetrakis(4-substituted phenyl)porphyrins at the liquid-graphite interface were investigated by scanning tunneling microscopy. We found that the presence of a small amount of a polar solvent, i.e., only 0.5 vol% of octanoic acid in phenyloctane, significantly affected the selective formation of the face-on polymorph over the edge-on one likely due to the solvent-molecule interactions at the 2D interface.

Efficient synthesis of halo indanones via chlorosulfonic acid mediated Friedel-Crafts cyclization of aryl propionic acids and their use in alkylation reactions

Sharma, Anil K.,Subramani, Amutha V.,Gorman, Christopher B.

, p. 389 - 395 (2007/10/03)

Several halo indanones were synthesized from benzyl Meldrum's acid derivatives in two steps. Although several Lewis acids are effective for the Friedel-Crafts ring-closing reaction on more electron-rich arenes, in the case of the electron-deficient arenes this chemistry is not efficient. Here it is reported that chlorosulfonic acid (used as solvent) is an efficient reagent for cyclization of electron-withdrawing arenes. These molecules are potentially useful for subsequent alkylation reactions. The selective alkylation of 5,7-dibromo indanone is demonstrated using Pd-catalyzed Grignard coupling to provide monoalkylated indanone in good yield.

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