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Benzenemethanesulfenothioic acid, R,R-diphenyl-, also known as (R,R)-benzenemethanesulfenothioic acid, diphenyl-, is an organic compound with the chemical formula C14H12O2S3. It is a chiral molecule, meaning it has a non-superimposable mirror image, and is characterized by its two phenyl groups attached to a central benzene ring through a sulfur atom. Benzenemethanesulfenothioic acid,R,R-diphenyl- is a type of sulfenothioic acid, which is a sulfur-containing organic acid. It is used in various chemical reactions and synthesis processes, particularly in the preparation of chiral ligands and catalysts. Due to its unique structure and properties, it plays a significant role in the field of asymmetric synthesis and organosulfur chemistry.

3492-71-5

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3492-71-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3492-71-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,9 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3492-71:
(6*3)+(5*4)+(4*9)+(3*2)+(2*7)+(1*1)=95
95 % 10 = 5
So 3492-71-5 is a valid CAS Registry Number.

3492-71-5SDS

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 triphenylmethane hydrodisulfide

1.2 Other means of identification

Product number -
Other names Triphenylmethylhydrodisulfid

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:3492-71-5 SDS

3492-71-5Relevant academic research and scientific papers

Understanding hydrogen sulfide storage: Probing conditions for sulfide release from hydrodisulfides

Bailey, T. Spencer,Zakharov, Lev N.,Pluth, Michael D.

, p. 10573 - 10576 (2014/08/18)

Hydrogen sulfide (H2S) is an important biological signaling agent that exerts action on numerous (patho)physiological processes. Once generated, H2S can be oxidized to generate reductant-labile sulfane sulfur pools, which include hydrodisulfides/persulfides. Despite the importance of hydrodisulfides in H2S storage and signaling, little is known about the physical properties or chemical reactivity of these compounds. We report here the synthesis, isolation, and characterization (NMR, IR, Raman, HRMS, X-ray) of a small-molecule hydrodisulfide and highlight its reactivity with reductants, nucleophiles, electrophiles, acids, and bases. Our experimental results establish that hydrodisulfides release H2S upon reduction and that deprotonation results in disproportionation to the parent thiol and S0, thus providing a mechanism for transsulfuration in the sulfane sulfur pool.

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