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34761-82-5

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34761-82-5 Usage

General Description

3,5-dimethyl-4-nitroaniline is a chemical compound with the molecular formula C8H10N2O2. It is a yellow crystalline solid with a molecular weight of 166.18 g/mol. 3,5-dimethyl-4-nitroaniline is commonly used as a precursor in the synthesis of dyes, pigments, and pharmaceuticals. Its chemical structure consists of a benzene ring with a nitro group (-NO2) and two methyl groups (-CH3) attached to the amino group (-NH2). 3,5-dimethyl-4-nitroaniline is considered to be a hazardous substance and should be handled with care due to its potential health and environmental hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 34761-82-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,7,6 and 1 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 34761-82:
(7*3)+(6*4)+(5*7)+(4*6)+(3*1)+(2*8)+(1*2)=125
125 % 10 = 5
So 34761-82-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H10N2O2/c1-5-3-7(9)4-6(2)8(5)10(11)12/h3-4H,9H2,1-2H3

34761-82-5SDS

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 3,5-dimethyl-4-nitroaniline

1.2 Other means of identification

Product number -
Other names 3,5-Dimethyl-4-nitro-anilin

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:34761-82-5 SDS

34761-82-5Relevant articles and documents

Benzo heterocyclic derivatives

-

Paragraph 0160; 0162; 0165; 0166, (2017/12/30)

Provided is a compound of general formula (I) as a potassium channel regulator and pharmaceutically acceptable equivalents thereof. The compound can be used in the preparation of medicines for increasing the ion flow in the potassium channel of mammals or

Nitration and Bromination of N-(dimethylphenyl)methanesulfonamides

Al-Khafaji, Sarah,Cardinale, Nina,Hanson, James R.

, p. 701 - 714 (2007/10/03)

The orientation of the products of nitrosation: nitration and bromination of the methanesulfonamides of the six isomeric dimethylanilines have been established by 1H NMR nuclear Overhauser experiments.

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