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3-(benzylsulfanyl)thiophene is an organic compound characterized by a thiophene ring, which is a five-membered aromatic ring containing one sulfur atom. This particular compound has a benzylsulfanyl group attached to the third carbon of the thiophene ring. The benzylsulfanyl group consists of a benzyl moiety (a phenyl ring with a methyl group attached) and a sulfanyl group (a sulfur atom bonded to a hydrogen atom). This combination results in a molecule with potential applications in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals due to its unique structure and reactivity. The compound's properties, such as its solubility and stability, can be influenced by the presence of the benzylsulfanyl group, making it a valuable building block in organic synthesis.

7511-65-1

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7511-65-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7511-65-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,1 and 1 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7511-65:
(6*7)+(5*5)+(4*1)+(3*1)+(2*6)+(1*5)=91
91 % 10 = 1
So 7511-65-1 is a valid CAS Registry Number.

7511-65-1SDS

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 3-benzylsulfanylthiophene

1.2 Other means of identification

Product number -
Other names 3-benzylthiothiophene

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:7511-65-1 SDS

7511-65-1Relevant academic research and scientific papers

Synthesis of benzyl sulfidesviasubstitution reaction at the sulfur of phosphinic acid thioesters

Nishiyama, Yoshitake,Hosoya, Takamitsu,Yoshida, Suguru

supporting information, p. 5771 - 5774 (2020/06/03)

An ambident electrophilicity of phosphinic acid thioesters is disclosed. Unexpected carbon-sulfur bond formation took place in the reaction between phosphinic acid thioesters and benzyl Grignard reagents. The developed method for benzyl sulfides has a wide substrate scope and was applicable for the synthesis of a drug analog.

1,2-Dithiins and precursors, XVII: Synthesis and properties of thieno anellated 1,2-dithiins, structural influence on colour

Schroth, Werner,Hintzsche, Ekkehard,Jordan, Hartwig,Jende, Thomas,Spitzner, Roland,Thondorf, Iris

, p. 7509 - 7528 (2007/10/03)

Various thieno[3,2-c] anellated (5a, 26) and dithieno[3,2-c:2,3-e] anellated 1,2-dithiins (32 a-c, 45) were obtained starting from appropriate thiophene precursors. The absorption maxima covered the range from 430 to 467 nm indicating olefinic rather than aromatic character of the anellating thiophene units. Access to the isomeric thieno[2,3-c] anellated series failed due to competing reactions in the final stage, e.g. by the formation of the 12-membered cyclic bis-disulfide 53.

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