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95433-16-2

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95433-16-2 Usage

General Description

3-(2-Phenoxyphenyl)acrylic acid is a chemical compound with the molecular formula C15H12O3. It is a member of the acrylic acid family, which are organic compounds that contain a carbon-carbon double bond and a carboxylic acid functional group. 3-(2-Phenoxyphenyl)acrylic acid is primarily used in the synthesis of various pharmaceutical and agricultural compounds. It is also used as a key intermediate in the production of dyes, pigments, and other specialty chemicals. Due to its versatile properties and numerous potential applications, 3-(2-Phenoxyphenyl)acrylic acid is of interest to researchers and manufacturers within the chemical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 95433-16-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,4,3 and 3 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 95433-16:
(7*9)+(6*5)+(5*4)+(4*3)+(3*3)+(2*1)+(1*6)=142
142 % 10 = 2
So 95433-16-2 is a valid CAS Registry Number.
InChI:InChI=1/C15H12O3/c16-15(17)11-10-12-6-4-5-9-14(12)18-13-7-2-1-3-8-13/h1-11H,(H,16,17)/b11-10+

95433-16-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(2-Phenoxyphenyl)acrylic acid

1.2 Other means of identification

Product number -
Other names 2-phenoxy-trans-cinnamic 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:95433-16-2 SDS

95433-16-2Relevant articles and documents

Structural isomers of cinnamic hydroxamic acids block HCV replication via different mechanisms

Kozlov, Maxim V.,Konduktorov, Konstantin A.,Malikova, Alsu Z.,Kamarova, Kamila A.,Shcherbakova, Anastasia S.,Solyev, Pavel N.,Kochetkov, Sergey N.

, (2019/09/30)

A set of ortho-, meta- and para-substituted cinnamic hydroxamic acids (CHAs) was synthesized. In each series of structural isomers, a phenyl substituent was linked to an aromatic ring of the parent cinnamic acid via a linker of one to four atoms in length

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