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1-Chloro-2,5-dimethyl-4-nitrobenzene and 2-Chloro-5-nitro-p-xylene are both organic compounds characterized by the presence of chlorine and nitro groups attached to a benzene ring. The former has chlorine, methyl, and nitro groups substituted into a benzene ring, while the latter contains a benzene ring with chlorine and nitro groups and two methyl groups on adjacent carbons, forming a dimethylbenzene or xylene structure. Both compounds are likely lipophilic due to their aromatic ring structure.

34633-69-7

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34633-69-7 Usage

Uses

Used in Chemical Synthesis:
1-Chloro-2,5-dimethyl-4-nitrobenzene and 2-Chloro-5-nitro-p-xylene are used as intermediates in the synthesis of various organic compounds. Their unique structures make them valuable building blocks for the production of dyes, pharmaceuticals, and other specialty chemicals.
Used in Plastics Industry:
Due to their lipophilic nature, these compounds may be used in the plastics industry to modify the properties of polymers, such as improving their stability, durability, or resistance to environmental factors.
Used in Dyes Industry:
The presence of chlorine and nitro groups in these compounds may contribute to their color properties, making them suitable for use in the dyes industry to produce a range of colored products.
Used in Research and Development:
1-Chloro-2,5-dimethyl-4-nitrobenzene and 2-Chloro-5-nitro-p-xylene can be used in research and development settings to study the effects of different functional groups on the properties of organic compounds and to develop new synthetic methods or applications.
Note: The potential for these compounds to be harmful or explosive under certain conditions should be considered when determining their suitability for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 34633-69-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,6,3 and 3 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 34633-69:
(7*3)+(6*4)+(5*6)+(4*3)+(3*3)+(2*6)+(1*9)=117
117 % 10 = 7
So 34633-69-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H8ClNO2/c1-5-4-8(10(11)12)6(2)3-7(5)9/h3-4H,1-2H3

34633-69-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Chloro-2,5-dimethyl-4-nitrobenzene

1.2 Other means of identification

Product number -
Other names 1-chloro-2,5-dimethyl-4-nitro-benzene

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:34633-69-7 SDS

34633-69-7Relevant academic research and scientific papers

PYRAZOLYL DERIVATIVES USEFUL AS ANTI-CANCER AGENTS

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Page/Page column 207, (2021/06/26)

The present application provides a compound of formula (I) or a stereoisomer thereof, or an atropisomer thereof, or a pharmaceutically acceptable salt thereof, or a pharmaceutically acceptable salt of a stereoisomer thereof, or a pharmaceutically acceptable salt of an atropisomer thereof; method for manufacturing said compound, and its therapeutic uses. The present application further provides a combination of pharmacologically active agents and a pharmaceutical composition comprising said compound.

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

Henichart, J. P.,Bernier J. L.,Vaccher, C.,Houssin, R.,Warin, V.,Baert, F.

, p. 3535 - 3542 (2007/10/02)

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.

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