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30651-62-8

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30651-62-8 Usage

Chemical class

Arylalkylamines

Derivative

Piperazine

Contains

Phenylmethylene group

Potential use

Pharmaceutical applications

Investigated for

Use as a drug or building block in medicinal chemistry

Importance

Molecular structure and properties

Ongoing research

Pharmacological and therapeutic properties, efficacy, and safety for clinical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 30651-62-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,6,5 and 1 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 30651-62:
(7*3)+(6*0)+(5*6)+(4*5)+(3*1)+(2*6)+(1*2)=88
88 % 10 = 8
So 30651-62-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H15N3/c1-2-4-11(5-3-1)10-13-14-8-6-12-7-9-14/h1-5,10,12H,6-9H2/b13-10+

30651-62-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-phenyl-N-piperazin-1-ylmethanimine

1.2 Other means of identification

Product number -
Other names AP 8

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:30651-62-8 SDS

30651-62-8Downstream Products

30651-62-8Relevant articles and documents

Process development of a platelet aggregation inhibitor

Zanka, Atsuhiko

, p. 418 - 421 (1998)

A practical and efficient method for N-amination of piperazine via a nitrosoamine, suitable for a large scale synthesis, is described. This method involved the temporary transformation of an in situ prepared aminopiperazine to a hydrazone, allowing efficient separation of zinc salt byproducts from the system. Acylation and deprotection with hydroxylamine directly afforded FR062732 in satisfactory quality for pharmacological evaluation. These methods solved the operational problems usually inherent in zinc reduction of nitrosoamines.

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