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Benzaldehyde, 2-hydroxy-, (3-methyl-2-quinoxalinyl)hydrazone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

420106-35-0

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420106-35-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 420106-35-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,2,0,1,0 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 420106-35:
(8*4)+(7*2)+(6*0)+(5*1)+(4*0)+(3*6)+(2*3)+(1*5)=80
80 % 10 = 0
So 420106-35-0 is a valid CAS Registry Number.

420106-35-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(3-Methyl-quinoxalin-2-yl)-hydrazonomethyl]-phenol

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:420106-35-0 SDS

420106-35-0Downstream Products

420106-35-0Relevant academic research and scientific papers

Solvent free microwave accelerated synthesis of heterocyclic thiazolidin-4-ones as antimicrobial and antifungal agents

Sekhar, Kondapalli Venkata Gowri Chandra,Rao, Vajja Sambasiva,Reddy, Aravalli Satish,Sunandini, Ravada,Kumar Satuluri

scheme or table, p. 1219 - 1222 (2010/09/18)

A simple and efficient method has been developed for conversion of arenecarbaldehyde-3-methylquinoxalin-2-ylhydrazones to 3-(2-methylquinoxalin-3- yl)-2-(substitutedphenyl)thiazolidin-4-ones in good yields using microwave irradiation technique on silica a

Positive allosteric modulators of the metabotropic glutamate receptor subtype 4 (mGluR4). Part II: Challenges in hit-to-lead

Williams, Richard,Niswender, Colleen M.,Luo, Qingwei,Le, Uyen,Conn, P. Jeffrey,Lindsley, Craig W.

experimental part, p. 962 - 966 (2009/09/25)

This Letter describes the synthesis and SAR of two mGluR4 positive allosteric modulator leads, 6 and 7. VU001171 (6) represents the most potent (EC50 = 650 nM), efficacious (141% Glu Max) and largest fold shift (36-fold) of any mGluR4 PAM repor

Synthesis and antimicrobial activity of 2-substituted benzyl hydrazino-3-methyl quinoxalines

Vyas,Chauhan,Parikh

, p. 972 - 974 (2007/10/03)

Reduction of 3-methyl-2-(arylidcne hydrazino)quinoxalines 5a-1 with NaBH4 in controlled experimental conditions to give the 2-substituted benzyl hydrazine-3-methyl quinoxalines 6a-l have been described. The structure of compounds 6a-l have been confirmed from elemental analysis, IR, 1H NMR and mass spectral data. All the compounds have been screened for their antimicrobial activity against several microbes.

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