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3-Succinimidoglutarimide, DL- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

19246-23-2

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19246-23-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19246-23-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,2,4 and 6 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 19246-23:
(7*1)+(6*9)+(5*2)+(4*4)+(3*6)+(2*2)+(1*3)=112
112 % 10 = 2
So 19246-23-2 is a valid CAS Registry Number.

19246-23-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name α-Succinimido-glutarimid

1.2 Other means of identification

Product number -
Other names 3-(2,5-Dioxo-pyrrolidin-1-yl)-piperidine-2,6-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:19246-23-2 SDS

19246-23-2Downstream Products

19246-23-2Relevant academic research and scientific papers

A Novel Green Synthesis of Thalidomide and Analogs

Benjamin, Ellis,Hijji, Yousef M.

, (2017)

Thalidomide and its derivatives are currently under investigation for their antiangiogenic, immunomodulative, and anticancer properties. Current methods used to synthesize these compounds involve multiple steps and extensive workup procedures. Described herein is an efficient microwave irradiation green synthesis method that allows preparation of thalidomide and its analogs in a one-pot multicomponent synthesis system. The multicomponent synthesis system developed involves an array of cyclic anhydrides, glutamic acid, and ammonium chloride in the presence of catalytic amounts of 4-N,N-dimethylaminopyridine (DMAP) to produce thalidomide and structurally related compounds within minutes in good isolated yields.

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