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34743-49-2

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34743-49-2 Usage

General Description

4-methoxy-2,6-dimethyl-aniline is a chemical compound with the molecular formula C9H13NO. It is an aromatic amine and aniline derivative, commonly utilized as an intermediate in the synthesis of dyes, pharmaceuticals, and other organic compounds. This chemical is characterized by its methoxy and dimethyl substituents on the aromatic ring, imparting specific physical and chemical properties to the molecule. It is important to handle 4-methoxy-2,6-dimethyl-aniline with caution, as exposure to this compound can cause irritation to the eyes, skin, and respiratory system, and may have potential harmful effects on human health and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 34743-49-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,7,4 and 3 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 34743-49:
(7*3)+(6*4)+(5*7)+(4*4)+(3*3)+(2*4)+(1*9)=122
122 % 10 = 2
So 34743-49-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H13NO/c1-6-4-8(11-3)5-7(2)9(6)10/h4-5H,10H2,1-3H3

34743-49-2SDS

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 4-Methoxy-2,6-dimethylaniline

1.2 Other means of identification

Product number -
Other names 2-Amino-5-methoxy-1.3-dimethyl-benzol

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:34743-49-2 SDS

34743-49-2Relevant articles and documents

B(C6F5)3-Catalyzed C-H Alkylation of N-Alkylamines Using Silicon Enolates without External Oxidant

Chan, Jessica Z.,Chang, Yejin,Wasa, Masayuki

supporting information, p. 984 - 988 (2019/02/14)

An efficient method for the coupling of N-alkylamines with silicon enolates to generate β-amino carbonyl compounds is disclosed. These reactions proceed by activation of α-amino C-H bonds by B(C6F5)3, which likely generate

PYRAZOLOPYRIMIDINE DERIVATIVES, PREPARATION METHOD THEREOF, AND PHARMACEUTICAL COMPOSITION FOR USE IN PREVENTING OR TREATING CANCER, AUTOIMMUNE DISEASE AND BRAIN DISEASE CONTAINING THE SAME AS AN ACTIVE INGREDIENT

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Paragraph 628-632, (2018/12/02)

The present invention relates to a pyrazolopyrimidine derivative, a preparation method thereof and a pharmaceutical composition comprising the same as an active ingredient for the prevention or treatment of cancer, autoimmune disease and brain disease. The pyrazolopyrimidine derivative of the present invention exhibits excellent Bruton's tyrosine kinase inhibition activity, so that it can be effectively used as a pharmaceutical composition for the prevention or treatment of cancer, autoimmune disease and Parkinson's disease.

Efficient copper-catalyzed amination of DNA-conjugated aryl iodides under mild aqueous conditions

Ruff, Yves,Berst, Frédéric

supporting information, p. 1188 - 1193 (2018/08/01)

Herein, we describe the development of copper-catalyzed cross-coupling of DNA-conjugated aryl iodides with aliphatic amines. This protocol leverages a novel ligand, 2-((2,6-dimethoxyphenyl)amino)-2-oxoacetic acid, to effect the transformation in aqueous D

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