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2,4-Dibromo-3-methylaniline is a chemical compound with the molecular formula C7H7Br2N. It is a derivative of aniline, characterized by a benzene ring with two bromine atoms and a methyl group attached to a nitrogen atom. 2,4-Dibromo-3-methylaniline is commonly used in organic synthesis and serves as an intermediate in the manufacturing of dyes and pharmaceuticals. It is known for its mild to moderate toxicity, which may cause skin and eye irritation upon contact, necessitating careful handling and storage with adherence to proper safety protocols.

80948-78-3

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80948-78-3 Usage

Uses

Used in Organic Synthesis:
2,4-Dibromo-3-methylaniline is used as a key intermediate in the synthesis of various organic compounds. Its unique molecular structure allows for the creation of a wide range of chemical products, making it a valuable component in the field of organic chemistry.
Used in Dye Manufacturing:
In the dye industry, 2,4-Dibromo-3-methylaniline is used as an intermediate for the production of dyes. Its chemical properties enable the development of a diverse array of dyes with different color characteristics, contributing to the vibrancy and variety of colors available in textiles and other applications.
Used in Pharmaceutical Production:
2,4-Dibromo-3-methylaniline is also utilized in the pharmaceutical industry as an intermediate in the synthesis of certain drugs. Its presence in the molecular structure of these compounds can influence their therapeutic properties, making it an essential component in the development of new medications.

Check Digit Verification of cas no

The CAS Registry Mumber 80948-78-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,9,4 and 8 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 80948-78:
(7*8)+(6*0)+(5*9)+(4*4)+(3*8)+(2*7)+(1*8)=163
163 % 10 = 3
So 80948-78-3 is a valid CAS Registry Number.

80948-78-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-dibromo-3-methylaniline

1.2 Other means of identification

Product number -
Other names (2,4-dibromo-3-methylphenyl)amine

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:80948-78-3 SDS

80948-78-3Downstream Products

80948-78-3Relevant academic research and scientific papers

Preparation of carbazole and dibenzofuran derivatives by selective bromination on aromatic rings or benzylic groups with N-bromosuccinimide

Fang, Lei,Zhang, Haun,Fang, Xubin,Gou, Shaohua,Cheng, Lin

, p. 635 - 641 (2014/06/23)

N-Bromosuccinimide (NBS), a bromine source, has been used to study the bromination of toluidine and cresols systematically to clarify the underlying mechanism and the orientation effect. It has been found that bromination of toluidine and cresols which possess electron-donating NH2/OH with NBS gives electrophilic aromatic substitution products quickly instead of the desired benzylic bromination products. In contrast, when the electronic effect of the substituted groups is reversed, only the benzylic bromination products are gained. Based on this methodology, several potential AChE inhibitors, such as 2-methoxy-5-(benzylamino)methyl-dibenzofuran, 3-bromo-2-methoxy-5-methyl-9H- carbazole, 3,6-dibromo-2-methoxy-5-methyl-9H-carbazole, and 5-(bromomethyl)-2- methoxy-9H-(phenylsulfonyl)-carbazole have been synthesized.

BENZIMIDAZOLE ANTIVIRAL AGENTS

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Page/Page column 131, (2011/09/14)

Provided are compounds of Formula (I) and (II) and pharmaceutically acceptable salts thereof, their pharmaceutical compositions, their methods of preparation, and their use for treating viral infections mediated by a member of the Flaviviridae family of viruses such as hepatitis C virus (HCV).

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