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1-CHLORO-2,4-DIMETHYL-5-NITRO-BENZENE, also known as nitrochloro-xylene, is a chemical compound characterized by its molecular formula C8H8ClNO2. It is a yellowish-brown solid with a molecular weight of 189.60 g/mol. 1-CHLORO-2,4-DIMETHYL-5-NITRO-BENZENE is recognized for its role as an intermediate in the synthesis of a variety of products, including pharmaceuticals, dyes, and agrochemicals. Additionally, it finds application in organic synthesis and serves as a reagent in chemical reactions. Due to its potentially hazardous nature, causing irritation to the skin, eyes, and respiratory system, and its harmful effects if ingested or inhaled in large quantities, 1-CHLORO-2,4-DIMETHYL-5-NITRO-BENZENE requires careful handling and adherence to proper safety precautions.

69383-68-2

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69383-68-2 Usage

Uses

Used in Pharmaceutical Industry:
1-CHLORO-2,4-DIMETHYL-5-NITRO-BENZENE is used as a chemical intermediate for the synthesis of various pharmaceuticals, contributing to the development of new medications and therapeutic agents.
Used in Dye Industry:
In the dye industry, 1-CHLORO-2,4-DIMETHYL-5-NITRO-BENZENE serves as an intermediate, playing a crucial role in the production of different types of dyes utilized in coloring textiles, plastics, and other materials.
Used in Agrochemical Industry:
1-CHLORO-2,4-DIMETHYL-5-NITRO-BENZENE is utilized as an intermediate in the synthesis of agrochemicals, which are essential for the development of pesticides and other agricultural products that protect crops and enhance yield.
Used in Organic Synthesis:
1-CHLORO-2,4-DIMETHYL-5-NITRO-BENZENE is employed in organic synthesis, where it acts as a building block for the creation of more complex organic molecules, expanding the scope of chemical research and product development.
Used as a Reagent in Chemical Reactions:
1-CHLORO-2,4-DIMETHYL-5-NITRO-BENZENE functions as a reagent in various chemical reactions, facilitating specific transformations and processes that are vital for the advancement of chemical science and technology.

Check Digit Verification of cas no

The CAS Registry Mumber 69383-68-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,3,8 and 3 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 69383-68:
(7*6)+(6*9)+(5*3)+(4*8)+(3*3)+(2*6)+(1*8)=172
172 % 10 = 2
So 69383-68-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H8ClNO2/c1-5-3-6(2)8(10(11)12)4-7(5)9/h3-4H,1-2H3

69383-68-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

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

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:69383-68-2 SDS

69383-68-2Relevant academic research and scientific papers

ISOINDOLINONE COMPOUNDS

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Page/Page column 165, (2021/04/17)

Disclosed herein is a compound or pharmaceutically acceptable salts or stereoisomers thereof of of formula I wherein X1 is linear or branched C1-6 alkyl, C3-6 cycloalkyl, -C1-6 alkyl C3-6 cycloalkyl, C6-10 aryl, 5-10 membered heteroaryl, C1-6 alkyl C6-10 aryl, C1-6 alkyl 5-10 membered heteroaryl, wherein X1 is unsubstituted or substituted with one or more of halogen, linear or branched C1-6 alkyl, linear or branched C1-6 heteroalkyl, CF3, CHF2, -O-CHF2, -O-(CH2)2-OMe, OCF3, C1-6 alkylamino, -CN, -N(H)C(O)-C1- 6alkyl, -OC(O)-C1-6alkyl, -OC(O)-C1-4alkylamino, -C(O)O-C1-6alkyl, -COOH, - CHO, -C1-6alkylC(O)OH, -C1-6alkylC(O)O-C1-6alkyl, NH2, C1-6 alkoxy or C1-6 alkylhydroxy; X2 is hydrogen, C6-10 aryl, 5-10 membered heteroaryl, -O-(5-10 membered heteroaryl), 4-8 membered heterocycloalkyl, C1-4 alkyl 4-8 membered heterocycloalkyl, -O-(4-8 membered heterocycloalkyl), -O-C1-4 alkyl-(4-8 membered heterocycloalkyl), -OC(O)-C1-4alkyl-4-8 membered heterocycloalkyl or C6 aryloxy, wherein X2 is unsubstituted or substituted with one or more of linear or branched C1-6 alkyl, NH2, NMe2 or 5-6 membered heterocycloalkyl; n is 0, 1 or 2.

A new route to prepare 6-chloro-5-(2-chloroethyl)oxindole

Gurjar, Mukund K.,Murugaiah,Reddy, Dandepally Srinivasa,Chorghade, Mukund S.

, p. 309 - 312 (2013/09/06)

6-Chloro-5-(2-chloroethyl)oxindole, a key intermediate in the manufacturing of the antipsychotic drug, ziprasidone, has been synthesized by a new route. The salient features of the synthesis are (1) bis-dialkylation of 2,4-difluoro-5-chloronitrobenzene with sodium diethyl malonate, (2) decarboxylative hydrolysis to obtain the oxindole derivative, and (3) reduction and chlorination of acetic ester side chain.

PYRAZINO(AZA)INDOLE DERIVATIVES

-

, (2008/06/13)

Chemical compounds of formula (I): and pharmaceutically acceptable salts and addition compounds and prodrugs thereof are useful in therapy, particularly for the treatment of disorders of the central nervous system; damage to the central nervous system; ca

Bis(dealkoxycarbonylation) of nitroarylmalonates: A facile entry to alkylated nitroaromatics

Gurjar,Reddy,Murugaiah,Murugaiah

, p. 1659 - 1661 (2007/10/03)

A simple approach to alkylated nitroaromatics from substituted nitroaryl malonic esters by double decarboxylation is detailed.

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