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3-(biphenyl-4-yl)-3-oxopropanoic acid is a chemical compound with the molecular formula C15H12O3. It is a derivative of propanoic acid, featuring a biphenyl-4-yl group attached to the third carbon atom. This organic compound is characterized by its ketone and carboxylic acid functional groups, which contribute to its reactivity and potential applications in various chemical processes. The compound is known for its role in the synthesis of certain pharmaceuticals and as an intermediate in the production of specialty chemicals. Its structure, with a central three-carbon chain and a biphenyl ring, endows it with unique electronic and steric properties that can be exploited in organic synthesis.

7497-69-0

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7497-69-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7497-69-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,9 and 7 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7497-69:
(6*7)+(5*4)+(4*9)+(3*7)+(2*6)+(1*9)=140
140 % 10 = 0
So 7497-69-0 is a valid CAS Registry Number.

7497-69-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-oxo-3-(4-phenylphenyl)propanoic acid

1.2 Other means of identification

Product number -
Other names 1-Biphenyl-4-yl-2-formyloxy-aethanon

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:7497-69-0 SDS

7497-69-0Downstream Products

7497-69-0Relevant academic research and scientific papers

A sustainable byproduct catalyzed domino strategy: Facile synthesis of α-formyloxy and acetoxy ketones via iodination/nucleophilic substitution/hydrolyzation/oxidation sequences

Zhu, Yan-Ping,Gao, Qing-He,Lian, Mi,Yuan, Jing-Jing,Liu, Mei-Cai,Zhao, Qin,Yang, Yan,Wu, An-Xin

supporting information; experimental part, p. 12700 - 12702 (2012/01/03)

The sustainable byproduct catalyzed domino strategy has been performed for the facile synthesis of α-formyloxy and acetoxy ketones via iodination/nucleophilic substitution/hydrolyzation/oxidation sequences from simple and readily available aromatic ketone

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