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54433-51-1

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54433-51-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54433-51-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,4,3 and 3 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 54433-51:
(7*5)+(6*4)+(5*4)+(4*3)+(3*3)+(2*5)+(1*1)=111
111 % 10 = 1
So 54433-51-1 is a valid CAS Registry Number.

54433-51-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-phenyl-1-prop-2-enylpyrrolidine-2,5-dione

1.2 Other means of identification

Product number -
Other names 1-Allyl-3-phenyl-pyrrolidin-2,5-dion

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:54433-51-1 SDS

54433-51-1Downstream Products

54433-51-1Relevant articles and documents

Ruthenium(II)-Catalyzed Hydroarylation of Maleimides Using Carboxylic Acids as a Traceless Directing Group

Mandal, Anup,Sahoo, Harekrishna,Dana, Suman,Baidya, Mahiuddin

supporting information, p. 4138 - 4141 (2017/08/15)

An efficient Ru(II)-catalyzed hydroarylation of maleimides with ready-stock aryl carboxylic acids has been developed based on weak carboxylate-directed ortho-C-H alkylation and concomitant decarboxylation processes, fabricating 3-aryl succinimides, a recurrent scaffold in drug molecules, in high yields (up to 97%). The protocol features operational simplicity, avoids the need for precious metal additives/oxidants, and offers broad substrate scope with formal meta- and para-selectivities. It represents the first example of Ru(II)-catalyzed direct arylation of maleimides with unbiased benzoic acids.

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