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1-Butanesulfonothioic acid, S-phenyl ester, also known as phenyl butanesulfonothioate, is an organic compound with the chemical formula C10H13O2S2. It is a colorless to pale yellow liquid with a molecular weight of 239.34 g/mol. 1-Butanesulfonothioic acid, S-phenyl ester is characterized by the presence of a phenyl group (C6H5) attached to a butanesulfonothioic acid moiety, which consists of a butane chain (C4H10) with a sulfonothioic acid group (-SO2SH) attached to it. 1-Butanesulfonothioic acid, S-phenyl ester, is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is also known for its potential applications in the development of new materials and as a reagent in organic synthesis. Due to its chemical structure, it exhibits properties such as solubility in organic solvents and reactivity towards nucleophiles, making it a versatile building block in chemical research and industry.

4160-31-0

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4160-31-0 Usage

Common Use

Reagent in organic synthesis

Physical State

Colorless to pale yellow liquid

Odor

Faint

Flammability

Highly flammable

Chemical Function

Acts as a sulfur transfer reagent

Applications

a. Production of chemicals and pharmaceuticals
b. Stabilizer in manufacturing of plastics
c. Additive in production of lubricants and fuels

Safety Precautions

a. Can cause skin and eye irritation upon contact
b. Harmful if inhaled or ingested
c. Handle with care

Check Digit Verification of cas no

The CAS Registry Mumber 4160-31-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,6 and 0 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4160-31:
(6*4)+(5*1)+(4*6)+(3*0)+(2*3)+(1*1)=60
60 % 10 = 0
So 4160-31-0 is a valid CAS Registry Number.

4160-31-0Downstream Products

4160-31-0Relevant academic research and scientific papers

Synthesis of Symmetrical and Unsymmetrical Thiosulfonates from Disulfides through Electrochemically Induced Disulfide Bond Metathesis and Site-Selective Oxidation

Strehl, Julia,Hilt, Gerhard

, (2022)

The anodic generation of symmetrical and unsymmetrical thiosulfonates is presented. First, the oxidation of disulfides yielding symmetrical thiosulfonates was realized. The direct synthesis is performed using a simple quasi-divided cell design, whereby using a supporting electrolyte is unnecessary. Its principle was then expanded to the conversion of unsymmetrical disulfides that were generated in situ through metathesis of two symmetrical disulfides. This enables a direct access to unsymmetrical thiosulfonates without any pre-functionalization or elaborate synthesis of the starting materials for the first time. The reaction scope was investigated by converting differently functionalized aliphatic and aromatic disulfides in moderate to very good yields. Furthermore, a sensitivity assessment for an improved reproducibility and a robustness screen to determine the compatibility of the reaction against functional groups were performed.

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