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2,5-Pyrrolidinedione, 3-(4-fluorophenyl)-1-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

716-02-9

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716-02-9 Usage

Molecular weight

290.27 g/mol

Appearance

Solid

Main use

Intermediate in the synthesis of various drugs and pharmaceutical products

Therapeutic properties

Anti-inflammatory, analgesic effects

Potential applications

Inhibitor of certain enzymes involved in cancer and other diseases progression, drug development, and medical research.

Check Digit Verification of cas no

The CAS Registry Mumber 716-02-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,1 and 6 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 716-02:
(5*7)+(4*1)+(3*6)+(2*0)+(1*2)=59
59 % 10 = 9
So 716-02-9 is a valid CAS Registry Number.

716-02-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-fluorophenyl)-1-methylpyrrolidine-2,5-dione

1.2 Other means of identification

Product number -
Other names 3-(4-fluoro-phenyl)-1-methyl-pyrrolidine-2,5-dione

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:716-02-9 SDS

716-02-9Downstream Products

716-02-9Relevant academic research and scientific papers

Pd(II)/bipyridine catalyzed conjugate addition of arylboronic acids to α,β-unsaturated amides

Ji, Jiamin,Yang, Zhenyu,Liu, Rui,Ni, Yuxin,Lin, Shaohui,Pan, Qinmin

, p. 2723 - 2726 (2016)

The Pd(II)/bipyridine-catalyzed conjugate addition of arylboronic acid to α,β-unsaturated amides was developed and optimized, and the reaction was proceeded smoothly in air. A series of arylboronic acid and α,β-unsaturated amide substrates were surveyed, and modest to excellent yields were given.

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