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6-(4-CHLOROPHENYL)-6-OXOHEXANOIC ACID is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56721-40-5

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56721-40-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56721-40-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,7,2 and 1 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 56721-40:
(7*5)+(6*6)+(5*7)+(4*2)+(3*1)+(2*4)+(1*0)=125
125 % 10 = 5
So 56721-40-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H13ClO3/c13-10-7-5-9(6-8-10)11(14)3-1-2-4-12(15)16/h5-8H,1-4H2,(H,15,16)

56721-40-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-(4-CHLOROPHENYL)-6-OXOHEXANOIC ACID

1.2 Other means of identification

Product number -
Other names 5-(4-Chlor-benzoyl)-valeriansaeure

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:56721-40-5 SDS

56721-40-5Relevant academic research and scientific papers

Selective C-C Bond Cleavage of Cycloalkanones by NaNO2/HCl

He, Tianyu,Chen, Dengfeng,Qian, Shencheng,Zheng, Yu,Huang, Shenlin

, p. 6525 - 6529 (2021/09/02)

A novel selective fragmentation of cycloalkanones by NaNO2/HCl has been established. The C-C bond cleavage reaction proceeds smoothly under mild conditions, selectively affording versatile keto acids or oxime acids. The methodology can streamline the synthesis of valuable chiral molecules and isocoumarins from readily available feedstocks.

Aralkanamidophenyl compounds

-

, (2008/06/13)

This disclosure describes novel substituted aralkanamidobenzoic acids and analogs thereof. These compounds are useful pharmaceutical agents for ameliorating atherosclerosis by inhibiting the formation and development of atherosclerotic lesions in the arterial wall of mammals.

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