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(4-Methoxyphenyl)-(5-methyl-6H-thieno<2,3-b>pyrrol-4-yl)methanon is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

134327-86-9

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134327-86-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 134327-86-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,3,2 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 134327-86:
(8*1)+(7*3)+(6*4)+(5*3)+(4*2)+(3*7)+(2*8)+(1*6)=119
119 % 10 = 9
So 134327-86-9 is a valid CAS Registry Number.

134327-86-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-Methoxyphenyl)-(5-methyl-6H-thieno[2,3-b]pyrrol-4-yl)methanon

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:134327-86-9 SDS

134327-86-9Downstream Products

134327-86-9Relevant academic research and scientific papers

Thiophene as a structural element of physiologically active compounds. 19. The synthesis of substituted (6H-thieno[2,3-b]pyrrol-4-yl)phenylmethanones

Binder,Schnait,Rovenszky,Enzenhofer,Stroissnig

, p. 219 - 221 (2007/10/02)

The synthesis of 4-Methoxyphenyl-[5-methyl-6-(2-(4-morpholinyl)-ethyl)-6H-thieno[2,3- b]pyrrol-4-yl)phenylmethanone (1), a thiophene analogue of the analgesic Pravadoline B, is described. Starting with the acetylprotected thienylhydrazine 2b compound 7 was obtained in a Fischer-analogue cyclication in two steps. Use of the BOC-protected thienylhydrazine 2a yielded the pyrazol 5. Alkylation of 7 with N-(2-Chloroethyl)morpholine gave the target compound 1. In the acetylcholine-writhing-test in mice as well as in the acetic acid-writhing-test in rats 1 showed a significant lower antinociceptive activity than Pravadolin (B).

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