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[(E)-2-benzylsulfanylethenyl]sulfanylmethylbenzene is a complex organic molecule characterized by its benzene ring core, with two sulfur atoms and a reactive ethenyl group. The molecule also features a benzyl group attached to one of the sulfur atoms, which may affect its physical and chemical properties. This unique structure and the presence of various functional groups make it a promising candidate for applications in organic chemistry and material science.

53959-54-9

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53959-54-9 Usage

Uses

Used in Organic Synthesis:
[(E)-2-benzylsulfanylethenyl]sulfanylmethylbenzene is used as a key intermediate in the synthesis of various organic compounds due to its reactive ethenyl group and unique structure. The presence of the sulfur atoms and the benzyl group allows for a wide range of chemical reactions, making it a versatile building block in the development of new molecules with potential applications in various industries.
Used in Material Science:
In the field of material science, [(E)-2-benzylsulfanylethenyl]sulfanylmethylbenzene can be utilized as a component in the development of novel materials with specific properties. [(E)-2-benzylsulfanylethenyl]sulfanylmethylbenzene's unique structure and functional groups may contribute to the creation of materials with enhanced characteristics, such as improved stability, reactivity, or selectivity, depending on the desired application.
Used in Pharmaceutical Industry:
[(E)-2-benzylsulfanylethenyl]sulfanylmethylbenzene may also find applications in the pharmaceutical industry, where its unique structure and functional groups can be exploited for the design and synthesis of new drugs. [(E)-2-benzylsulfanylethenyl]sulfanylmethylbenzene's potential reactivity and the presence of sulfur atoms may allow for the development of molecules with specific biological activities, targeting various diseases and medical conditions.
Used in Chemical Research:
As a complex organic molecule with a unique structure, [(E)-2-benzylsulfanylethenyl]sulfanylmethylbenzene can be employed in chemical research to study various aspects of organic chemistry, such as reaction mechanisms, stereochemistry, and the influence of functional groups on molecular properties. [(E)-2-benzylsulfanylethenyl]sulfanylmethylbenzene can serve as a model system for understanding the behavior of similar molecules and for developing new synthetic strategies and methodologies.

Check Digit Verification of cas no

The CAS Registry Mumber 53959-54-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,9,5 and 9 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 53959-54:
(7*5)+(6*3)+(5*9)+(4*5)+(3*9)+(2*5)+(1*4)=159
159 % 10 = 9
So 53959-54-9 is a valid CAS Registry Number.

53959-54-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name [(E)-2-benzylsulfanylethenyl]sulfanylmethylbenzene

1.2 Other means of identification

Product number -
Other names 1,2-Bis-benzylmercapto-aethen

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:53959-54-9 SDS

53959-54-9Relevant academic research and scientific papers

Skeletal reorganization of mercaptoacetaldehyde dialkyl acetal in acid: formation of disulphide, 1,2-bis(mercapto)ethylene and 1,1,2-tris(mercapto)ethane derivatives

Ong, Chi Wi,Yen, Sin Fei,Chou, Yi Meen

, p. 601 - 605 (2007/10/03)

The reaction of mercaptoacetaldehyde dialkyl acetals 1a-c in the presence of sulfuric acid, polyphosphoric acid and zinc chloride is described. Other than the disulfide reported previously, new compounds 1,2-bis-(mercapto)ethylene, 1,2,3-tris-(mercapto)ethane and 1,2-bis-(mercapto)methane have been isolated for the first time.

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