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182067-66-9

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182067-66-9 Usage

Reactivity

Highly reactive

Hazard potential

Potentially hazardous

Uses

Commonly used in chemical research and laboratory experiments as a building block for the synthesis of various organic compounds

Chemical reactions

Known for its ability to undergo various chemical reactions, making it an important reagent in organic chemistry

Research status

Precise properties and potential applications are still under research and investigation

Safety precautions

Proper safety precautions must be taken when handling this chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 182067-66-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,2,0,6 and 7 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 182067-66:
(8*1)+(7*8)+(6*2)+(5*0)+(4*6)+(3*7)+(2*6)+(1*6)=139
139 % 10 = 9
So 182067-66-9 is a valid CAS Registry Number.

182067-66-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-acetyl-1,3-dimethylpiperazine-2,5-dione

1.2 Other means of identification

Product number -
Other names 2,5-Piperazinedione,4-acetyl-1,3-dimethyl-(9CI)

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:182067-66-9 SDS

182067-66-9Downstream Products

182067-66-9Relevant articles and documents

Selectivity in radical reactions of alanylglycine anhydride derivatives

Chai, Christina L.L.,Hay, Darren B.,King, Alison R.

, p. 605 - 610 (2007/10/03)

Functionalization of N,N′-disubstituted alanylglycine anhydrides under radical conditions is described. The radical (7), generated (i) from reactions of N,N′-disubstituted alanylglycine anhydrides with N-bromosuccinimide, and (ii) from related bromo compounds by reaction with tributyltin deuteride, undergoes carbon-bromine and carbon-deuterium bond formation with moderate to high diastereoselectivities depending on the N-substituents present.

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