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64512-90-9

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64512-90-9 Usage

Type of compound

Hydrazine derivative

Specific type

Monoester hydrazide

Usage

a. Synthesis of pharmaceuticals
b. Synthesis of agrochemicals
c. Organic chemical reactions

Potential application

Corrosion inhibitor in metal surfaces

Hazardous nature

Yes, should be handled with proper care and precautions

Further research

Necessary to fully understand potential uses and risks

Check Digit Verification of cas no

The CAS Registry Mumber 64512-90-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,5,1 and 2 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 64512-90:
(7*6)+(6*4)+(5*5)+(4*1)+(3*2)+(2*9)+(1*0)=119
119 % 10 = 9
So 64512-90-9 is a valid CAS Registry Number.

64512-90-9SDS

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 tert-butyl N-(hydrazinecarbonylamino)carbamate

1.2 Other means of identification

Product number -
Other names tert-butyloxycarbonylcarbazide

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:64512-90-9 SDS

64512-90-9Relevant articles and documents

Carbonylhydrazide-based molecular tongs inhibit wild-type and mutated HIV-1 protease dimerization

Dufau, Laure,Marques Ressurrei??o, Ana Sofia,Fanelli, Roberto,Kihal, Nadjib,Vidu, Anamaria,Milcent, Thierry,Soulier, Jean-Louis,Rodrigo, Jordi,Desvergne, Audrey,Leblanc, Karine,Bernadat, Guillaume,Crousse, Benoit,Reboud-Ravaux, Micheèle,Ongeri, Sandrine

, p. 6762 - 6775 (2012/10/08)

We have designed and synthesized new molecular tongs based on a rigid naphthalene scaffold and evaluated their antidimer activity on HIV-1 protease (PR). We inserted carbonylhydrazide and oligohydrazide (azatide) fragments into their peptidomimetic arms t

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