609-92-7

Basic information

• Product Name: 2,5-Dimethyl-1,3-dinitrobenzene
• Synonyms: 2,5-Dimethyl-1,3-dinitrobenzene;2,6-dinitro-p-xylene
• CAS NO: 609-92-7
• Molecular Formula: C₈H₈N₂O₄
• Molecular Weight: 196.16
• Mol File: 609-92-7.mol
• Article Data: 12

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,5-Dimethyl-1,3-dinitrobenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 2,5-Dimethyl-1,3-dinitrobenzene(609-92-7)
• EPA Substance Registry System: 2,5-Dimethyl-1,3-dinitrobenzene(609-92-7)

Safety Data

• Hazardous Substances Data: 609-92-7(Hazardous Substances Data)

Usage

General Description

2,5-Dimethyl-1,3-dinitrobenzene, also known as sym-dinitrobenzene or 2,5-dimethyl-1,3-dinitrobenzol, is a chemical compound with the formula C8H8N2O4. It is a pale yellow solid that is primarily used as an intermediate in the production of dyes, pharmaceuticals, and other organic compounds. It is a powerful explosive compound and has been used in the manufacturing of ammunition and explosives. However, due to its toxicity and potential health hazards, its use has been limited and it is largely considered to be a hazardous substance that requires careful handling and proper safety protocols. Additionally, it is classified as a substance of very high concern under the Registration, Evaluation, Authorization and Restriction of Chemicals (REACH) regulation in the European Union.

Upstream product

• 89-58-7 mononitro-p-xylene 
• 106-42-3 para-xylene 
• 7697-37-2 nitric acid 
• 6311-52-0 3,6-dimethyl-2,4-dinitro-aniline 

Downstream Products

• 90764-89-9 6-methyl-1H-indazol-4-amine 
• 880086-93-1 6-methyl-4-nitro-1H-indole 
• 880086-94-2 ethyl 2,5-dimethyl-3-nitrophenylimidoformate 
• 90086-91-2 3-Amino-2,5-dimethyl-phenol 
• 65151-57-7 3-nitro-2,5-dimethylphenol 
• 35111-99-0 2,6-dinitro-terephthalic acid-4-ethyl ester 
• 69824-99-3 3,5-dinitrobenzene-1,4-dioic acid 
• 62564-50-5 2,5-dimethyl-3-nitroaniline 
• 51136-52-8 2,6-diamino-p-xylene 

Relevant articles and documents

Nitration of deactivated aromatic compounds via mechanochemical reaction

A variety of deactivated arenes were nitrated to their corresponding nitro derivatives in excellent yields under high-speed ball milling condition using Fe(NO3)3·9H2O/P2O5 as nitrating reagent. A radical involved mechanism was proposed for this facial, eco-friendly, safe, and effective nitration reaction.

Method for synthesizing 2,6-dinitroterephthalic acid (by machine translation)

The reaction solution is subjected to post-treatment 2,6 - to obtain,dinitroterephthalic acid: and then the reaction solution is heated to, for, minutes, and then the reaction solution is heated to a reflux reaction 30 °C for, hours after the reaction sys

TRICYCLIC ANILIDE HETEROCYCLIC CGRP RECEPTOR ANTAGONISTS

Compounds of formula I: wherein variables A1, A2, B, m, n, J, R4, G1, G2, G3 and Y are as described herein, which are antagonists of CGRP receptors and which are useful in the treatment or prevention of diseases in which the CGRP is involved, such as migraine. The invention is also directed to pharmaceutical compositions comprising these compounds and the use of these compounds and compositions in the prevention or treatment of such diseases in which CGRP is involved.