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73383-82-1

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73383-82-1 Usage

Structure

A derivative of the pyrrole-2,5-dione with a methyl group at the 3 position and a phenylmethyl group at the 1 position.

Appearance

White to off-white crystalline solid.

Molecular weight

213.23 g/mol.

Uses

Primarily used in research and pharmaceutical applications as a building block for the synthesis of various organic compounds.

Importance

Unique structure and properties make it a valuable intermediate in the production of pharmaceuticals and other fine chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 73383-82-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,3,8 and 3 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 73383-82:
(7*7)+(6*3)+(5*3)+(4*8)+(3*3)+(2*8)+(1*2)=141
141 % 10 = 1
So 73383-82-1 is a valid CAS Registry Number.

73383-82-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzyl-3-methylpyrrole-2,5-dione

1.2 Other means of identification

Product number -
Other names 2-methyl-N-benzylmaleimide

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:73383-82-1 SDS

73383-82-1Relevant articles and documents

“On water” nano-Cu2O-catalyzed CO-free one-pot multicomponent cascade cyanation-annulation-aminolysis reaction toward phthalimides

Wen, Xiaowei,Liu, Xiaojuan,Yang, Zhiqi,Xie, Menglan,Liu, Yuxi,Long, Lipeng,Chen, Zhengwang

supporting information, p. 1738 - 1743 (2021/03/14)

An efficient nano-Cu2O-catalyzed cascade multicomponent reaction of 2-halobenzoic acids and trimethylsilyl cyanide with diverse amines was developed using water as a solvent, affording versatileN-substituted phthalimide derivatives in moderate to excellent yields. This novel strategy features carbon monoxide gas-free, environmentally benign, one-pot multistep transformation, commercially available reagents, a cheap catalyst without any additives, wide functional group tolerance, and operational convenience.

ANTIMICROBIAL COMPOUNDS AND METHODS

-

Paragraph 00704, (2020/07/31)

The invention is directed to compounds that are active as antibacterial agents. The invention compounds are active against gram-positive and gram-negative bacteria and can be used to treat infections caused by gram-positive and gram-negative bacteria. Also disclosed are processes and intermediates for making the compounds.

First total synthesis of 5-hydroxy-3-methyl-4-propylsulfanyl-5 h -furan-2-one: A cancer chemopreventive agent

Borikar, Sanjay P.,Paul, Vincent,Puranik, Vedavati G.,Sathe, Vilas T.,Lagunas-Rivera, Selene,Ordonez, Mario

experimental part, p. 1595 - 1598 (2011/06/24)

The first total synthesis of 5-hydroxy-3-methyl-4-propylsulfanyl-5H-furan- 2-one, a newly discovered natural product with anticancer property is described by two different routes. A sequence involving an incorporation of a methyl group via a Gilman reagent and a chemoselective reduction of a cyclic anhydride functionality are the key steps. The methods proposed start from easily available starting materials and allow ready preparation of the final compound in good overall yield. Georg Thieme Verlag Stuttgart · New York.

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