102169-99-3

Basic information

• Product Name: 2-broMo-4-Methyl-5-nitrobenzenaMine
• Synonyms: 2-broMo-4-Methyl-5-nitrobenzenaMine;2-BroMo-4-Methyl-5-nitro-phenylaMine;BenzenaMine, 2-broMo-4-Methyl-5-nitro-
• CAS NO: 102169-99-3
• Molecular Formula: C₇H₇BrN₂O₂
• Molecular Weight: 231.04668
• Mol File: 102169-99-3.mol

Chemical Properties

• Melting Point: 119-120 °C(Solv: ethyl acetate (141-78-6); hexane (110-54-3))
• Boiling Point: 336.8±37.0 °C(Predicted)
• Appearance: /
• Density: 1.698±0.06 g/cm3(Predicted)
• Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature
• PKA: 0.98±0.10(Predicted)
• CAS DataBase Reference: 2-broMo-4-Methyl-5-nitrobenzenaMine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-broMo-4-Methyl-5-nitrobenzenaMine(102169-99-3)
• EPA Substance Registry System: 2-broMo-4-Methyl-5-nitrobenzenaMine(102169-99-3)

Safety Data

• Hazardous Substances Data: 102169-99-3(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
2-Bromo-4-Methyl-5-Nitrobenzenamine is used as an intermediate in the synthesis of various pharmaceuticals. Its unique chemical structure allows it to be a key component in the development of new drugs with potential therapeutic benefits.
Used in Dye Industry:
In the dye industry, 2-broMo-4-Methyl-5-nitrobenzenaMine is used as an intermediate for the production of various dyes. Its chemical properties enable the creation of dyes with specific color characteristics and stability.
Used in Agrochemical Industry:
2-Bromo-4-Methyl-5-Nitrobenzenamine is also used in the production of agrochemicals. Its presence in these compounds can contribute to the development of effective pesticides and other agricultural products.
Used as a Reagent in Organic Chemical Reactions:
In the field of organic chemistry, 2-broMo-4-Methyl-5-nitrobenzenaMine serves as a reagent in various chemical reactions. Its ability to participate in different types of reactions makes it a valuable tool for synthesizing a wide range of organic compounds.
Overall, 2-Bromo-4-Methyl-5-Nitrobenzenamine is a versatile chemical compound with applications across multiple industries, including pharmaceuticals, dyes, agrochemicals, and organic chemical reactions. Its unique properties and potential for use in the development of new materials and compounds make it an important substance in research and industrial applications.

Upstream product

• 583-68-6 2-bromo-p-toluidine 
• 5411-53-0 5-bromo-2,4-dinitro-toluene 
• 412935-32-1 2-bromo-4-methyl-5-nitroformanilide 
• 7664-93-9 sulfuric acid 

Downstream Products

• 16503-61-0 acetic acid-(2-bromo-4-methyl-5-nitro-anilide) 
• 412935-32-1 2-bromo-4-methyl-5-nitroformanilide 
• 101580-70-5 4,5-dibromo-2-nitro-toluene 

Relevant articles and documents

AMINOPYRAZOLE DERIVATIVES

An objective of the present invention is to provide low-molecular-weight compounds that can inhibit Src family kinases. The present invention relates to compounds represented by general formula (I) or pharmacologically acceptable salts thereof. In the formula, Ar1 is optionally substituted C6-10 arylene or 5- to 10-membered heteroarylene, and Ar2 is optionally substituted C6-10 aryl or 5- to 10-membered heteroaryl. R1 and R2 are defined as described in the specification.

Synthesis of symmetric dinitro-functionalised troeger's base analogues

The synthesis of six new examples of 2,8-dinitro-substituted Troeger's base analogues are reported, together with the first examples of 1,7-, 3,9- and 4,10-dinitro Troeger's base analogues and the first example of a tetranitro Troeger's base compound. Several of these dinitro compounds lack substituents at the 2- and 8-positions and therefore provide further examples of Troeger's base analogues derived from anilines lacking a para substituent.

Photochromic properties of ortho-methylnitrobenzothiazoles in Solution

Isomeric benzothiazoles having the nitro and methyl groups ortho to each other are converted into tautomeric aci-nitro derivatives on irradiation in heptane solution; in water, the corresponding more deeply colored anions are formed. The efficiency of pho

RADICAL-ANIONS OF AROMATIC COMPOUNDS. XVI. ELECTRONIC STRUCTURE OF RADICAL-ANIONS AND THE DIRECTION OF PARTIAL REDUCTION OF DISUBSTITUTED DERIVATIVES OF m-DINITROBENZENE: THE RELATIVE EFFECTS OF THE SUBSTITUENTS

It was shown by means of compounds labeled with the 15N isotope that the radical-anions of a wide range of 1,5-disubstituted 2,4-dinitrobenzenes are in most cases characterized by localization of the density of the unpaired electron at one of the nitro groups.It was concluded that the substituents can be arranged in the following order according to their ability to stabilize the form with the negatively charged nitro group at the para position: CO2- > CH3 Br > Cl N(C2H5)2 > CN > OCH3; CO2- > I.The relative effectiveness of the substituents which stabilize the form of the radical-anions with the negatively charged nitro group at the ortho position was determined theoretically as follows: OCH3 +C5H5 +H(C2H5)2.The position of the substituents in the series given above are determined by the combined effect of such factors as the effective volume, the electronic effect transmitted through the skeleton, the field effect, and the ability to form intramolecular hydrogen bonds.It was shown that the direction of partial reduction of the derivatives of m-dinitrobenzene can be predicted on the basis of data on the electronic structure of their radical-anions, which are probable key intermediates of the processes.