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ethyl 2-[2-(4-chlorophenyl)hydrazinylidene]butanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

77373-59-2

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77373-59-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77373-59-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,3,7 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 77373-59:
(7*7)+(6*7)+(5*3)+(4*7)+(3*3)+(2*5)+(1*9)=162
162 % 10 = 2
So 77373-59-2 is a valid CAS Registry Number.

77373-59-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-(2-(4-chlorophenyl)hydrazono)butanoate

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:77373-59-2 SDS

77373-59-2Relevant academic research and scientific papers

Superior inhibition of influenza virus hemagglutinin-mediated fusion by indole-substituted spirothiazolidinones

Cihan-üstünda?, G?k?e,Zopun, Muhammet,Vanderlinden, Evelien,Ozkirimli, Elif,Persoons, Leentje,?apan, Gültaze,Naesens, Lieve

, (2019/11/26)

The influenza virus hemagglutinin (HA) mediates membrane fusion after viral entry by endocytosis. The fusion process requires drastic low pH-induced HA refolding and is prevented by arbidol and tert-butylhydroquinone (TBHQ). We here report a class of supe

Synthesis & Reaction of Indole-1,2-dicarboxaldehydes with Hydrazine & Hydroxylamine

Hiremath, Shivayogi P.,Thakar, Shreeram B.,Purohit, Muralidhar G.

, p. 770 - 774 (2007/10/02)

Indole-1,2-dicarboxaldehydes (2a-g) have been prepared by formylation of 3-methylindole-2-carboxaldehydes (1a-g) with DMF-POCl3 at 140 deg C. 2a-e react with N2H4.H2O to give hydrazones (3a-e and 3g) of 1-formylindole-2-carboxaldehydes instead of the tria

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