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1H-Pyrrole, 1-[2-(ethylthio)phenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

107344-51-4

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107344-51-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 107344-51-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,3,4 and 4 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 107344-51:
(8*1)+(7*0)+(6*7)+(5*3)+(4*4)+(3*4)+(2*5)+(1*1)=104
104 % 10 = 4
So 107344-51-4 is a valid CAS Registry Number.

107344-51-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-ethylsulfanylphenyl)pyrrole

1.2 Other means of identification

Product number -
Other names -

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:107344-51-4 SDS

107344-51-4Relevant academic research and scientific papers

Interrupted Pummerer Rearrangement: Capture of Tricoordinate Sulfur Species Generated under Pummerer Rearrangement Conditions

Bates, Dallas K.,Winters, R. Thomas,Picard, Joseph A.

, p. 3094 - 3097 (1992)

A new approach to fused N,S-heterocycles is described.Treatment of N-(2-(alkylsulfinyl)phenyl)pyrroles (5) under conditions which typically promote reaction at the carbon α to the sulfoxide group (i.e., the TFAA-initiated Pummerer rearrangement) produces selectively either pyrrolobenzothiazole (9) or 1-(trifluoroacetyl)pyrrolobenzothiazole (7).It is suggested the process occurs by reaction of the pyrrole nucleus at sulfur of the corresponding O-trifluoroacetylated sulfoxide 1 producing an intermediate S-alkylpyrrolobenzothiazolium salt 3.Nucleophilic displacement of the S-alkyl substituent by the trifluoroacetate counterion liberates pyrrolobenzothiazole, which may undergo trifluoroacetylation in the presence of excess TFAA.This approach to sulfur activation for intramolecular cyclizations is superior to other methods (usually involving positive halogen and a sulfide) since polyhalogenation and the instability of derivative halopyrroles are avoided.

An interrupted Pummerer reaction induced by hypervalent iodine(III) reagent: A new synthesis of pyrrolo[2,1-b]benzothiazole

Chen, Ling-Ching,Wang, Huey-Min,Kang, Iou-Jiun

, p. 1437 - 1441 (2007/10/03)

Treatment of 1-(2-alkylthiophenyl)pyrroles with phenyliodine(III) bis(trifluoroacetate) containing trifluoroacetic acid resulted in an interrupted Pummerer reaction to give pyrrolo[2,1-b]benzothiazole rather than the normal Pummerer-type products.

Intramolecular Sulfenylation Using Sulfoxides Praparation of 5H-Pyrrolobenzothiazines

Picard, Joseph A.,Chen, Shaowu,Bates, Dallas K.

, p. 1775 - 1790 (2007/10/02)

N-pyrrole (4) undergoes transfer sulfenylation to N-(2-chloromethylphenyl)-2-phenylthiopyrrole (5') presumably via S-phenyl 5H-pyrrolobenzothiazonium chloride (7).Depending upon the rigor of the reaction conditi

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