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50709-35-8

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50709-35-8 Usage

Chemical Properties

white to light yellow crystal powde

Check Digit Verification of cas no

The CAS Registry Mumber 50709-35-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,7,0 and 9 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 50709-35:
(7*5)+(6*0)+(5*7)+(4*0)+(3*9)+(2*3)+(1*5)=108
108 % 10 = 8
So 50709-35-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H6Cl2N2.ClH/c7-4-1-2-5(8)6(3-4)10-9;/h1-3,10H,9H2;1H

50709-35-8 Well-known Company Product Price

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  • Aldrich

  • (152781)  2,5-Dichlorophenylhydrazinehydrochloride  98%

  • 50709-35-8

  • 152781-5G

  • 420.03CNY

  • Detail

50709-35-8SDS

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 2,5-Dichlorophenylhydrazine hydrochloride

1.2 Other means of identification

Product number -
Other names 2,5-Dichlorophenylhydrazine Hydrochloride

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:50709-35-8 SDS

50709-35-8Relevant articles and documents

Discovery of pyrano[3,4-b]indoles as potent and selective HCV NS5B polymerase inhibitors

Gopalsamy, Ariamala,Lim, Kitae,Ciszewski, Gregory,Park, Kaapjoo,Ellingboe, John W.,Bloom, Jonathan,Insaf, Shabana,Upeslacis, Janis,Mansour, Tarek S.,Krishnamurthy, Girija,Damarla, Murthy,Pyatski, Yelena,Ho, Douglas,Howe, Anita Y. M.,Orlowski, Mark,Feld, Boris,O'Connell, John

, p. 6603 - 6608 (2007/10/03)

A novel series of HCV NS5B RNA-dependent RNA polymerase inhibitors containing a pyrano-[3,4-b]indole scaffold is described leading to the discovery of compound 16, a highly potent and selective inhibitor that is active in the replicon system.

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