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1H-Indole, 1-(phenylmethyl)-3-(phenylsulfinyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

98508-70-4

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98508-70-4 Usage

Derivative of indole

A heterocyclic aromatic compound commonly found in plants and used in the production of pharmaceuticals and perfumes.

Contains a phenylmethyl group

A benzyl group attached to a phenyl ring.

Contains a phenylsulfinyl group

A phenyl ring attached to a sulfur atom, which is bonded to a hydrogen atom.

Potential pharmaceutical applications

The presence of the phenylmethyl and phenylsulfinyl groups make it a potential candidate for the development of new drugs or medications.

Unique chemical reactivity and biological activity

The sulfinyl group may confer unique chemical and biological properties to the compound, making it of interest in the field of medicinal chemistry and drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 98508-70-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,5,0 and 8 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 98508-70:
(7*9)+(6*8)+(5*5)+(4*0)+(3*8)+(2*7)+(1*0)=174
174 % 10 = 4
So 98508-70-4 is a valid CAS Registry Number.

98508-70-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-benzyl-3-(phenylsulfinyl)indole

1.2 Other means of identification

Product number -
Other names 1-benzyl-3-phenylsulfinylindole

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:98508-70-4 SDS

98508-70-4Relevant academic research and scientific papers

Desulfurization of Diaryl(heteroaryl) Sulfoxides with Benzyne

Chen, De-Li,Sun, Yan,Chen, Mengyuan,Li, Xiaojin,Zhang, Lei,Huang, Xin,Bai, Yihui,Luo, Fang,Peng, Bo

supporting information, (2019/06/13)

Two benzyne-enabled desulfurization reactions have been demonstrated which convert diaryl sulfoxides and heteroaryl sulfoxides to biaryls and desulfurized heteroarenes, respectively. The reaction accessing biaryls tolerates a variety of functional groups, such as halides, pseudohalides, and carbonyls. Mechanistic studies reveal that both reactions proceed via a common assembly process but divergent disassemblies of the generated tetraaryl(heteroaryl) sulfuranes.

1,2,3-trisubstituted indoles for treatment of inflammation

-

, (2008/06/13)

Disclosed are compounds of the formula STR1 wherein the several groups are defined herein. These compounds are useful for treating inflammation.

A NOVEL SYNTHESIS OF 3-CYANOINDOLES AND A NEW ROUTE TO INDOLE-3-CARBOXYLIC ACID DERIVATIVES.

Garcia, Josefina,Greenhouse, Robert,Muchowski, Joseph M.,Ruiz, Jose Antonio

, p. 1827 - 1830 (2007/10/02)

2-Alkyl-3-cyanoindoles are obtained when 1-alkylmethyl-2-chloro-(or 2-phenylsulfonyl)-3-phenylsulfonylindoles are reacted with excess azide ion (90 deg C/DMF).The reaction is considered to occur by a fragmentation recombination process in which the Schiff

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