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120276-59-7

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120276-59-7 Usage

Chemical Properties

Colorless liquid

Uses

3-Chloro-6-chloromethylpyridazine is used as a reagent in the synthesis of functionalized tetrahydro(ethano)triazolo[3,4-a]phthalazines as selective GABAA receptor agonists at the α3 subunit.

Check Digit Verification of cas no

The CAS Registry Mumber 120276-59-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,2,7 and 6 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 120276-59:
(8*1)+(7*2)+(6*0)+(5*2)+(4*7)+(3*6)+(2*5)+(1*9)=97
97 % 10 = 7
So 120276-59-7 is a valid CAS Registry Number.

120276-59-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Chloro-6-(chloromethyl)pyridazine

1.2 Other means of identification

Product number -
Other names 3-chloro-6-(chloromethyl)pyridazine

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:120276-59-7 SDS

120276-59-7Relevant articles and documents

Benzimidazole derivatives, preparation methods and uses theirof

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Page/Page column 37, (2018/12/01)

The present invention relates to benzimidazole compounds useful in treating for protein kinase-associated disorders. There is also a need for compounds useful in the treatment or prevention of one or more symptoms of cancer, transplant rejections. Furthermore, there is a need for methods for modulating the activity of protein kinases, such as CDK4 and/or CDK6, using the compounds provided herein.

Imidazopyridazine hepatitis C virus polymerase inhibitors. Structure-activity relationship studies and the discovery of a novel, traceless prodrug mechanism

Leivers, Martin,Miller, John F.,Chan, Stephanie A.,Lauchli, Ryan,Liehr, Sebastian,Mo, Wenyan,Ton, Tony,Turner, Elizabeth M.,Youngman, Michael,Falls, J. Greg,Long, Susan,Mathis, Amanda,Walker, Jill

supporting information, p. 1964 - 1975 (2014/04/03)

By reducing the basicity of the core heterocycle in a series of HCV NS5B inhibitors, the hERG liability was reduced. The SAR was then systematically explored in order to increase solubility and enable dose escalation while retaining potency. During this e

METHODS FOR TREATING HCV

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Page/Page column 59, (2013/03/28)

This invention relates to combinations of therapeutic molecules useful for treating hepatitis C virus infection. The present invention relates to methods, uses, dosing regimens, and compositions.

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