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

63930-81-4

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63930-81-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63930-81-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,9,3 and 0 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 63930-81:
(7*6)+(6*3)+(5*9)+(4*3)+(3*0)+(2*8)+(1*1)=134
134 % 10 = 4
So 63930-81-4 is a valid CAS Registry Number.

63930-81-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(Ethoxymethyl)-4-methylpiperazine

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:63930-81-4 SDS

63930-81-4Relevant academic research and scientific papers

TRICYCLIC PYRAZOLE KINASE INHIBITORS

-

Page/Page column 57, (2008/06/13)

Compounds of the present invention are useful for inhibiting protein tyrosine kinases. Also disclosed are methods of making the compounds, compositions containing the compounds, and methods of treatment using the compounds.

Synthesis of unsymmetrical dinucleating ligands bearing nitrogen and oxygen donor atoms

Fenton, David E.,Papageorgiou, George

, p. 5913 - 5928 (2007/10/03)

The synthesis of unsymmetrical dinucleating ligands bearing nitrogen and oxygen donor atoms is described. The Schiff-base condensation of functionalised salicylaldehyde derivatives with primary amines gave rise to unsymmetrical unsaturated ligands, whereas condensation with secondary amines followed by in situ reduction of the iminium species with sodium borohydride, led to the formation of unsymmetrical saturated ligands. The latter were also prepared by the tandem Mannich reactions of 4-chlororesorcinol.

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