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26929-63-5

26929-63-5

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26929-63-5 Usage

General Description

2-(ethyldisulfanyl)benzoic acid is a chemical compound with the molecular formula C10H12O4S2. It is a derivative of benzoic acid and contains a disulfide group attached to an ethyl group. 2-(ethyldisulfanyl)benzoic acid is used in organic synthesis and pharmaceutical research, and it has been studied for its potential antioxidant and anti-inflammatory properties. Its structure suggests that it may have potential applications as a prodrug, capable of releasing active compounds when metabolized in the body. Further research is needed to fully understand the potential uses and effects of 2-(ethyldisulfanyl)benzoic acid.

Check Digit Verification of cas no

The CAS Registry Mumber 26929-63-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,9,2 and 9 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 26929-63:
(7*2)+(6*6)+(5*9)+(4*2)+(3*9)+(2*6)+(1*3)=145
145 % 10 = 5
So 26929-63-5 is a valid CAS Registry Number.

26929-63-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(ethyldisulfanyl)benzoic acid

1.2 Other means of identification

Product number -
Other names o-Carboxyphenyl ethyl disulfide

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:26929-63-5 SDS

26929-63-5Downstream Products

26929-63-5Relevant articles and documents

Asymmetric Disulfanylbenzamides as Irreversible and Selective Inhibitors of Staphylococcus aureus Sortase A

Barthels, Fabian,Bierlmeier, Jan,Distler, Ute,Hammerschmidt, Stefan,Konh?user, Matthias,Marciniak, Tessa,Marincola, Gabriella,Schirmeister, Tanja,Schwarzer, Dirk,Tenzer, Stefan,Wich, Peter R.,Ziebuhr, Wilma

supporting information, (2020/04/22)

Staphylococcus aureus is one of the most frequent causes of nosocomial and community-acquired infections, with drug-resistant strains being responsible for tens of thousands of deaths per year. S. aureus sortase A inhibitors are designed to interfere with

Conformationally constrained peptides and semipeptides derived from RGD as potent inhibitors of the platelet fibrinogen receptor and platelet aggregation

Ali,Bennett,Calvo,Elliott,Hwang,Ku,Lago,Nichols,Romoff,Shah,Vasko,Wong,Yellin,Yuan,Samanen

, p. 769 - 780 (2007/10/02)

Structure-activity studies have been pursued on cyclo-S,S-[Ac-Cys-(N(α)- Me)Arg-Gly-Asp-Pen]-NH2, 2 (SK and F 106760), a potent inhibitor of platelet aggregation, in an effort to improve potency and affinity for the GPIIb/IIIa receptor. Modific

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