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1000577-03-6

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1000577-03-6 Usage

Derivative

Piperazine

Usage

Intermediate in the synthesis of pharmaceuticals and organic compounds

Physical state

White solid at room temperature

Solubility

Soluble in organic solvents

Applications

Production of various drugs, potential therapeutic applications, reagent in organic synthesis, building block in the development of new chemical compounds

Importance

Plays a significant role in the pharmaceutical and chemical industries due to its versatile applications

Check Digit Verification of cas no

The CAS Registry Mumber 1000577-03-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,0,5,7 and 7 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1000577-03:
(9*1)+(8*0)+(7*0)+(6*0)+(5*5)+(4*7)+(3*7)+(2*0)+(1*3)=86
86 % 10 = 6
So 1000577-03-6 is a valid CAS Registry Number.

1000577-03-6SDS

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 1,5-Diethyl-2-piperazinone

1.2 Other means of identification

Product number -
Other names -

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:1000577-03-6 SDS

1000577-03-6Downstream Products

1000577-03-6Relevant articles and documents

Preparation of Optically Active Piperazines from Ethyl (S)-2-(2-Alkyl-1-aziridinyl)acetates

Yahiro, Nobuhide,Ito, Shigekazu

, p. 321 - 322 (2007/10/02)

Reaction of ethyl (S)-2-(2-alkyl-1-aziridinyl)acetates with boron trifluoride etherate in a large excess of ethylamine or ammonia gives the corresponding optically active piperazines in good yields.These piperazines retain the configuration of the starting aziridines.

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