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3,5-dimethyl-4-nitroaniline is a chemical compound characterized by its molecular formula C8H10N2O2. It is a yellow crystalline solid with a molecular weight of 166.18 g/mol. 3,5-dimethyl-4-nitroaniline features a benzene ring with a nitro group (-NO2) and two methyl groups (-CH3) attached to the amino group (-NH2). Due to its potential health and environmental hazards, 3,5-dimethyl-4-nitroaniline is classified as a hazardous substance and requires careful handling.

34761-82-5

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34761-82-5 Usage

Uses

Used in Chemical Synthesis Industry:
3,5-dimethyl-4-nitroaniline is used as a precursor for the synthesis of dyes, pigments, and pharmaceuticals. Its unique chemical structure allows it to serve as a building block in the creation of various organic compounds, contributing to the development of a wide range of products in the chemical industry.
Used in Pharmaceutical Industry:
3,5-dimethyl-4-nitroaniline is used as an intermediate in the production of pharmaceuticals. Its chemical properties make it a valuable component in the synthesis of certain drugs, aiding in the development of new medications and therapies.
Used in Dye and Pigment Industry:
3,5-dimethyl-4-nitroaniline is used as a starting material in the manufacture of dyes and pigments. Its ability to form various organic compounds makes it an essential component in the production of colorants for textiles, plastics, and other materials.

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 academic research and scientific papers

Benzo heterocyclic derivatives

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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

Green recyclable CuO-CeO2 nanocomposite catalyzed amination of aryl halides with aqueous ammonia in water

Albadi, Jalal,Mansournezhad, Azam

, p. 396 - 398 (2014/06/10)

CuO-CeO2 nanocomposite as a green recyclable catalyst, catalyzed amination of aryl halides with aqueous ammonia in water. This catalyst can be easily recovered by simple filtration and recycled up to 5 consecutive runs with consistent activity. The procedure provides some advantages such as simple work-up, clean procedure, relatively short reaction times and high yields of the products. Efficient procedure for the amination of aryl halides catalyzed by Cu-CeO2 nanocomposite. Copyright

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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