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2-amino-4-(2,3-dimethoxyphenyl)-6-(2-methoxyphenyl)pyridine-3-carbonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

6958-12-9

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6958-12-9 Usage

Structure

Contains a pyridine ring and a carbonitrile functional group

Application

Used in medicinal and pharmaceutical research

Biological Activity

Potentially interacts with biological targets

Drug Development

Candidate for drug discovery and development

Interest in Research

Unique structure and properties warrant further study in chemistry and pharmacology

Check Digit Verification of cas no

The CAS Registry Mumber 6958-12-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,5 and 8 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6958-12:
(6*6)+(5*9)+(4*5)+(3*8)+(2*1)+(1*2)=129
129 % 10 = 9
So 6958-12-9 is a valid CAS Registry Number.

6958-12-9SDS

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 (Z)-N,N,N-trimethyl-2-(2-(naphthalen-1-ylmethylene)hydrazinyl)-2-oxoethan-1-aminium chloride

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:6958-12-9 SDS

6958-12-9Relevant academic research and scientific papers

Kinetics and Mechanism of the Formation of Girard T Hydrazones from Naphthaldehydes

Stachissini, Antonia Sonia,Amaral, Antonia T. do,Amaral, Luciano do

, p. 1929 - 1931 (2007/10/02)

In aqueous solution, Girard T hydrazone formation from naphthaldehydes does not proceed to completion under the conditions used.The corresponding equilibrium constants have been determined and employed to calculate the rate of the reaction at completion.For all the reactions studied, the pH-rate profiles, extrapolated to zero buffer concentration, show one break at pH 4-5, characteristic of a change in the rate-determining step from aminomethanol dehydration to aminomethanol formation on going from pH 7 to pH 1.The formation of the aminomethanol is subject to catalysis by hydronium ion and by carboxylic acids present in the buffers used to maintain pH.Brensted α values for this catalysis vary from 0.24 to 0.26.We suggest a stepwise preassociation mechanism for the reaction catalysed by carboxylic acids.

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