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3477-69-8

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3477-69-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3477-69-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,7 and 7 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3477-69:
(6*3)+(5*4)+(4*7)+(3*7)+(2*6)+(1*9)=108
108 % 10 = 8
So 3477-69-8 is a valid CAS Registry Number.

3477-69-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N'-[(E)-(2-hydroxy-4-oxocyclohexa-2,5-dien-1-ylidene)methyl]pyridine-4-carbohydrazide

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:3477-69-8 SDS

3477-69-8Downstream Products

3477-69-8Relevant articles and documents

Effective methods for the synthesis of hydrazones, quinazolines, and Schiff bases: Reaction monitoring using a chemometric approach

?ilovi?, Ivica,Cvijanovi?, Danijela,Hrenar, Tomica,Pavlovi?, Gordana,Pisk, Jana,Vrdoljak, Vi?nja

, p. 38566 - 38577 (2020/11/05)

Synthesis of hydrazones (1a-4a and 1b-4b), quinazolines (3c·MeOH and 3d·MeOH), and hydrazone-Schiff bases (4c and 4d) is achieved by combining suitable aldehydes (2,3- or 2,4-dihydroxybenzaldehyde) with four hydrazides (isonicotinic, nicotinic, and 2- or

Design, synthesis and in vitro antimalarial activity of an acylhydrazone library

Melnyk, Patricia,Leroux, Virginie,Sergheraert, Christian,Grellier, Philippe

, p. 31 - 35 (2007/10/03)

A library of acylhydrazone iron chelators was synthesized and tested for its ability to inhibit the growth of a chloroquine-resistant strain of Plasmodium falciparum. Some of these new compounds are significantly more active than desferrioxamine DFO, the

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