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732-91-2

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732-91-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 732-91-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,3 and 2 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 732-91:
(5*7)+(4*3)+(3*2)+(2*9)+(1*1)=72
72 % 10 = 2
So 732-91-2 is a valid CAS Registry Number.

732-91-2SDS

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 N'-[(Z)-(3-bromo-6-oxocyclohexa-2,4-dien-1-ylidene)methyl]pyridine-4-carbohydrazide

1.2 Other means of identification

Product number -
Other names 2-Hydroxy-5-brom-benzaldehyd-isonicotinoylhydrazon

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:732-91-2 SDS

732-91-2Downstream Products

732-91-2Relevant articles and documents

Synthesis, crystal structure, hirshfeld surface analysis, DFT calculations, anti-diabetic activity and molecular docking studies of (E)-N’-(5-bromo-2-hydroxybenzylidene) isonicotinohydrazide

Karrouchi, Khalid,Fettach, Saad,Jotani, Mukesh M.,Sagaama, Abir,Radi, Smaail,Ghabbour, Hazem A.,Mabkhot, Yahia N.,Himmi, Benacer,El Abbes Faouzi, My,Issaoui, Noureddine

, (2020)

In this present work, the newly synthesized compound E)-N’-(5-bromo-2-hydroxybenzylidene)isonicotinohydrazide (2) has been synthesized and characterized by IR, 1H &13C NMR, ESI-MS and single crystal X-ray diffraction analysis using e

Synthesis, spectral characterization, crystal structure and antibacterial studies of diorganotin(IV) complexes with isonicotinoyl hydrazone derivatives

Sedaghat, Tahereh,Yousefi, Maryam,Bruno, Giuseppe,Amiri Rudbari, Hadi,Motamedi, Hossein,Nobakht, Valiollah

, p. 88 - 96 (2014/06/10)

The new diorganotin(IV) complexes R2SnL (L = La: R = Me 1, Ph 2; L = Lb: R = Me 3, Ph 4, L = Lc: R = Me 5, Ph 6, Bu 7) have been synthesized by the reaction of the hydrazone ligands N′-(5-bromo-2-hydroxybenzylid

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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