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2(5H)-Thiophenone, 5-(phenylmethyl)-4-(1-pyrrolidinyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

117648-47-2

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117648-47-2 Usage

Class of organic compounds

thiophenones

+ Thiophene ring

five-membered ring with two carbon atoms and a sulfur atom

+ Phenylmethyl group

a phenyl group attached to a methyl group

+ Pyrrolidinyl group

a five-membered nitrogen-containing ring

Potential applications

industrial and pharmaceutical uses due to unique structure and properties.

Check Digit Verification of cas no

The CAS Registry Mumber 117648-47-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,6,4 and 8 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 117648-47:
(8*1)+(7*1)+(6*7)+(5*6)+(4*4)+(3*8)+(2*4)+(1*7)=142
142 % 10 = 2
So 117648-47-2 is a valid CAS Registry Number.

117648-47-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-benzyl-3-pyrrolidin-1-yl-2H-thiophen-5-one

1.2 Other means of identification

Product number -
Other names 5-Benzyl-2,5-dihydro-4-pyrrolidino-2-thiophen

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:117648-47-2 SDS

117648-47-2Relevant academic research and scientific papers

Novel synthesis and γ-alkylation reactions of 4-(1-pyrrolidinyl)-2(5H)-thiophenones

Li, Yu-Jang,Liu, Zen-Ting,Yang, Sheng-Chuan

, p. 8011 - 8013 (2001)

Four-step synthesis of achiral and chiral 4-(1-pyrrolidinyl)-2(5H)-thiophenones with 61 and 66% overall yields are described. The γ-alkylation reaction studies and synthetic applications toward the thiolactomycin analog are also reported.

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