15540-81-5

Basic information

• Product Name: 1-bromo-2,5-dimethyl-4-nitrobenzene
• Synonyms: 1-bromo-2,5-dimethyl-4-nitrobenzene
• CAS NO: 15540-81-5
• Molecular Formula: C₈H₈BrNO₂
• Molecular Weight: 230.06
• Mol File: 15540-81-5.mol

Chemical Properties

• Melting Point: 70 °C
• Boiling Point: 288.8±35.0 °C(Predicted)
• Appearance: /
• Density: 1.533±0.06 g/cm3(Predicted)
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 1-bromo-2,5-dimethyl-4-nitrobenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-bromo-2,5-dimethyl-4-nitrobenzene(15540-81-5)
• EPA Substance Registry System: 1-bromo-2,5-dimethyl-4-nitrobenzene(15540-81-5)

Safety Data

• Hazardous Substances Data: 15540-81-5(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
1-bromo-2,5-dimethyl-4-nitrobenzene is utilized 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, contributing to the advancement of medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, 1-bromo-2,5-dimethyl-4-nitrobenzene serves as an intermediate for the production of various agrochemicals. Its involvement in the synthesis process helps in creating effective compounds for agricultural applications, such as pesticides and herbicides.
Used in Dye and Pigment Production:
1-bromo-2,5-dimethyl-4-nitrobenzene is employed in the manufacturing of dyes and pigments due to its aromatic properties. Its ability to impart color makes it a valuable component in the creation of a wide range of colorants used in various industries, including textiles, plastics, and printing inks.

Upstream product

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Downstream Products

• 30273-40-6 4-bromo-2,5-dimethylaniline 
• 53258-93-8 2-(p-Tolylthio)-5-nitro-xylol 
• 13711-31-4 N-(4-bromo-2,5-dimethyl-phenyl)acetamide 
• 444002-66-8 1-(2,5-dimethyl-4-nitrophenyl)piperidin-2-one 
• 1202388-33-7 4-(2,5-dimethyl-4-(4-(5-methyl-1H-pyrazol-3-ylamino)-5-(trifluoromethyl)pyrimidin-2-ylamino)phenyl)cyclohexanone 
• 1202388-91-7 4-(4-(5-chloro-4-(5-methyl-1H-pyrazol-3-ylamino)pyrimidin-2-ylamino)-2,5-dimethylphenyl)-cyclohexanone oxime 
• 1202389-45-4 4-(4-(5-chloro-4-(5-methyl-1H-pyrazol-3-ylamino)pyrimidin-2-ylamino)-2,5-dimethylphenyl)cyclohexanone 
• 1202389-29-4 2,5-dimethyl-4-(1,4-dioxaspiro[4.5]decan-8-yl)aniline 
• 1202389-15-8 1-(2,5-dimethyl-4-nitrophenyl)-3-(dimethylamino)but-2-en-1-one 
• 1202389-20-5 2,5-dimethyl-4-(3-methyl-1H-pyrazol-5-yl)aniline 
• 1202389-21-6 5-(2,5-dimethyl-4-nitrophenyl)-3-methylpyrazol 
• 1202389-13-6 2,5-dimethyl-4-(3-methylisoxazol-5-yl)aniline 
• 1202389-16-9 5-(2,5-dimethyl-4-nitrophenyl)-3-methylisoxazole 

Relevant articles and documents

FORMIMIDAMIDINE COMPOUNDS USEFUL AGAINST PHYTOPATHOGENIC MICROORGANISMS

The present invention relates to 4-substituted amidine derivatives of the general formula (I), wherein A1-A4, D, L, Q, R7, R7' and integer's v and w have the meanings as defined in description. The invention further relates to methods for their preparation and use of said compounds to fight undesired phytopathogenic microorganisms, and agents for said purpose, comprising said amidine derivatives, all according to the invention. This invention further relates to a method for controlling undesired phytopathogenic microorganisms by application of said 4-substituted amidine derivatives of general formula (I) to such undesired microorganisms and/or to their habitat, according to the invention. (I)

CARBOLINE CARBOXAMIDE COMPOUNDS USEFUL AS KINASE INHIBITORS

Compounds having formula (I), and enantiomers, and diastereomers, stereoisomers, pharmaceutically-acceptable salts thereof, formula (I) are useful as kinase modulators, including Btk modulation.

ACCES AUX DINITRO-2,4 DIARYLAMINES PAR SUBSTITUTION NUCLEOPHILE SNAr-LIMITES DE LA REACTION ET APPLICATION A LA SYNTHESE DE CYANOCARBAZOLES

3-Cyanocarbazoles, key-intermediates in the total synthesis of pyrido carbazoles, have been obtained starting from easily available materials and involving the cyclization of diarylamines.The first step of the preparation consists in a SNAr reaction between a para substituted aniline and a chloro- (or bromo)-dinitrobenzene.This nucleophilic substitution has been found to be hindered by the steric effect of a methyl group, explained in terms of inhibition of resonance and confirmed by X-ray determination.