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481038-64-6

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481038-64-6 Usage

Chemical composition

Consists of a piperazine ring with a benzyl group and a carbobenzyloxy (CBZ) protecting group attached.

Use

Often used as an intermediate in the synthesis of pharmaceuticals and agrochemicals.

Potential

Has potential as a precursor in the production of designer drugs and illicit substances.

Classification

Categorized as a controlled substance in many jurisdictions due to its potential for abuse and its link to illegal drug manufacturing.

Safety measures

Strict safety measures should be followed when handling and using 1-N-CBZ-2-Benzyl piperazine to prevent any potential health hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 481038-64-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,8,1,0,3 and 8 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 481038-64:
(8*4)+(7*8)+(6*1)+(5*0)+(4*3)+(3*8)+(2*6)+(1*4)=146
146 % 10 = 6
So 481038-64-6 is a valid CAS Registry Number.

481038-64-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyl 2-benzylpiperazine-1-carboxylate

1.2 Other means of identification

Product number -
Other names B-1455

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:481038-64-6 SDS

481038-64-6Relevant articles and documents

PYRAZOLOPYRIDINE AMINE COMPOUNDS FOR THE TREATMENT OF AUTOIMMUNE DISEASE

-

Page/Page column 70-71, (2020/05/07)

The present invention relates to compounds of formula (I), wherein R1, R2, R3,R4 and X are as described herein, and their pharmaceutically acceptable salt, enantiomer or diastereomer thereof, and compositions in

High-Temperature Boc Deprotection in Flow and Its Application in Multistep Reaction Sequences

Bogdan, Andrew R.,Charaschanya, Manwika,Dombrowski, Amanda W.,Wang, Ying,Djuric, Stevan W.

supporting information, p. 1732 - 1735 (2016/05/19)

A simplified Boc deprotection using a high-temperature flow reactor is described. The system afforded the qualitative yield of a wide variety of deprotected substrates within minutes using acetonitrile as the solvent and without the use of acidic conditions or additional workups. Highly efficient, multistep reaction sequences in flow are also demonstrated wherein no extraction or isolation was required between steps.

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