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2436-92-2

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2436-92-2 Usage

General Description

3,4-Dimethylquinoline, also known as 3,4-lutidine, is an organic compound with the chemical formula C10H9N. It is a neutral, non-polar molecule that is a derivative of quinoline. 3,4-Dimethylquinoline is a colorless to pale yellow liquid that is insoluble in water but soluble in organic solvents. It is commonly used as a building block in the synthesis of various pharmaceuticals, dyes, and other organic compounds. Additionally, it is also used as a corrosion inhibitor and as an intermediate in the manufacture of rubber chemicals. This chemical is considered to be a hazardous material and should be handled with caution due to its potential health and environmental risks.

Check Digit Verification of cas no

The CAS Registry Mumber 2436-92-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,3 and 6 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2436-92:
(6*2)+(5*4)+(4*3)+(3*6)+(2*9)+(1*2)=82
82 % 10 = 2
So 2436-92-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H11N/c1-8-7-12-11-6-4-3-5-10(11)9(8)2/h3-7H,1-2H3

2436-92-2SDS

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 3,4-DIMETHYLQUINOLINE

1.2 Other means of identification

Product number -
Other names Quinoline,3,4-dimethyl

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:2436-92-2 SDS

2436-92-2Relevant articles and documents

Addition of propargyltrimethylsilane to N-methyleneamine equivalents: Generation and electrophilic cyclization of vinylic carbocations

Ha, Hyun-Joon,Lee, Young-Scong,Ahn, Young-Gil

, p. 2357 - 2364 (2007/10/03)

Lewis acid induced N-methyleneamine equivalents from N-(methoxymethyl)anilines or 1,3,5-triphenylhexahydro-1,3,5-triazines reacted with propargyltrimethylsilanes to give N-buta-2,3-dienylanilines, 4-methylene-1,2,3,4-tetrahydroquinolines and its oxidized product of 4-methylquinolines. These products came from branching reactions of the elimination and electrophilic aromatic substitution from the same vinylic carbocation intermediate.

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