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1-Piperazinecarboxamide, 4-acetyl- (6CI,9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

98337-79-2

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98337-79-2 Usage

Type of compound

Synthetic organic compound

Use in industry

Building block for the synthesis of various drugs and active pharmaceutical ingredients

Potential therapeutic applications

Central nervous system depressant, anxiolytic agent

Conditions treated

Schizophrenia, epilepsy, anxiety disorders

Structure

Simple

Availability

Commercially available for research and development purposes

Check Digit Verification of cas no

The CAS Registry Mumber 98337-79-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,3,3 and 7 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 98337-79:
(7*9)+(6*8)+(5*3)+(4*3)+(3*7)+(2*7)+(1*9)=182
182 % 10 = 2
So 98337-79-2 is a valid CAS Registry Number.

98337-79-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-acetylpiperazine-1-carboxamide

1.2 Other means of identification

Product number -
Other names 4-acetyl-1-piperazinecarboxamide

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:98337-79-2 SDS

98337-79-2Downstream Products

98337-79-2Relevant academic research and scientific papers

Process for producing aminopiperazine derivatives

-

, (2008/06/13)

A new industrial process excellent in yield and purity for preparing a compound of the formula: or a salt thereof in a less number of steps with a synthetic pathway without proceeding via nitroso compounds, wherein R1is lower aryl, ar(lower)alk

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