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6623-25-2

6623-25-2

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6623-25-2 Usage

Molecular structure

complex

Functional groups

Carboxymethylsulfanyl group
4-nitrophenylmethyl group
Central sulfanylacetic acid moiety

Acidic behavior

likely due to carboxylic acid and sulfhydryl functional groups

Reactivity

potential reactivity with nucleophiles

Redox reactions

ability to undergo reduction reactions

Potential

diverse range of chemical reactions and possible biological activities

Check Digit Verification of cas no

The CAS Registry Mumber 6623-25-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,2 and 3 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6623-25:
(6*6)+(5*6)+(4*2)+(3*3)+(2*2)+(1*5)=92
92 % 10 = 2
So 6623-25-2 is a valid CAS Registry Number.

6623-25-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[carboxymethylsulfanyl-(4-nitrophenyl)methyl]sulfanylacetic acid

1.2 Other means of identification

Product number -
Other names 4-Nitro-benzal-bis-thioglykolsaeure

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:6623-25-2 SDS

6623-25-2Relevant articles and documents

Solvent-free mechanochemical synthesis of bisthioglycolic acid derivatives: an efficient and versatile strategy for carbon–sulfur bond formation

Bhargava, Gaurav,Kumar, Rupesh,Naikoo, Rayees Ahmad,Singh, Parvesh

, (2021/10/07)

An eco-friendly, easily achievable and efficient strategy has been explored to synthesize functionalized bisthioglycolic acids using a variety of aldehydes and thioglycolic acid. The employed protocol is solvent free and provides the desirable products in

Mass spectral studies on some nitrobenzylidene thioacetal derivatives

Gohar, Gamal A.,Mahmoud, Mohamed E.

, p. 59 - 65 (2007/10/03)

The electron impact mass spectral studies on some nitrobenzylidene thioacetal derivatives showed two different mechanisms of oxygen transfer from the nitro group to the sulfur containing fragments via intra-and inter-oxygen transfer. The two mechanisms ar

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