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2,4-Dichloro-3-methyl-1,5-dinitrobenzene is a chemical compound characterized by its molecular formula C7H5Cl2N3O4. It presents as a yellow crystalline solid, which is insoluble in water but readily soluble in organic solvents such as acetone and ethanol. 2,4-Dichloro-3-methyl-1,5-dinitrobenzene is known for its applications in various industrial processes due to its chemical properties.

51676-76-7

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51676-76-7 Usage

Uses

Used in Chemical Synthesis:
2,4-Dichloro-3-methyl-1,5-dinitrobenzene is utilized as an intermediate in the production of dyes, pigments, and pharmaceuticals. Its unique structure allows it to be a key component in the synthesis of these complex organic compounds.
Used in Photographic Films:
In the photography industry, 2,4-Dichloro-3-methyl-1,5-dinitrobenzene serves as a sensitizing agent in the manufacture of photographic films. Its chemical properties enhance the light sensitivity of the film, improving the quality of the images captured.
Used in Medical Research:
2,4-Dichloro-3-methyl-1,5-dinitrobenzene has been studied for its potential as an anti-cancer agent and in the treatment of certain medical conditions. Its chemical structure may offer therapeutic benefits, although further research is necessary to fully understand its capabilities and safety.
It is crucial to handle 2,4-Dichloro-3-methyl-1,5-dinitrobenzene with care due to its toxic nature, which can cause irritation to the skin, eyes, and respiratory system if not properly managed.

Check Digit Verification of cas no

The CAS Registry Mumber 51676-76-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,6,7 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 51676-76:
(7*5)+(6*1)+(5*6)+(4*7)+(3*6)+(2*7)+(1*6)=137
137 % 10 = 7
So 51676-76-7 is a valid CAS Registry Number.

51676-76-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-dichloro-3-methyl-1,5-dinitrobenzene

1.2 Other means of identification

Product number -
Other names Benzene,2,4-dichloro-3-methyl-1,5-dinitro

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:51676-76-7 SDS

51676-76-7Relevant academic research and scientific papers

N-Phenyl heteroarylamine analogues of fluazinam using the intermediate derivatization methods approach

Guan, Aiying,Li, Huichao,Li, Zhinian,Yang, Fan,Xie, Yong,Yang, Xiaoping,Liu, Changling

, p. 1107 - 1114 (2014)

Twenty-one N-phenyl heteroarylamine analogues of fluazinam 3a-3u were prepared via nucleophilic substitution reaction of 2,6-dichloro-3,5- dinitrotoluene with heteroarylamines using the intermediate derivatization method. 2,6-Dichloro-3,5-dinitrotoluene,

Design, synthesis and structure-activity relationship of novel diphenylamine derivatives

Li, Huichao,Guan, Aiying,Huang, Guang,Liu, Chang-Ling,Li, Zhinian,Xie, Yong,Lan, Jie

, p. 453 - 461 (2016/01/25)

Diphenylamine derivatives have been reported with good fungicidal, insecticidal, acaricidal, rodenticidal and/or herbicidal activities. To find new lead compound of this kind, a series of novel diphenylamine derivatives were designed and synthesized by the approach of Intermediate Derivatization Methods. All compounds were identified by 1H NMR and elemental analysis. Bioassays demonstrated that some compounds substituted at 2,4,6-positions or 2,4,5-positions of phenyl ring B exhibited excellent fungicidal activities. The optimal compounds P30 and P33 showed 80% and 85% control respectively against cucumber downy mildew at 12.5 mg L-1, both 100% control against rice blast at 0.3 mg L-1 and both 100% control against cucumber gray mold at 0.9 mg L-1. The relationship between structure and fungicidal activities was discussed as well.

INTEGRATED PROCESS FOR THE PREPARATION OF POLYBENZIMIDAZOLE PRECURSORS

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Page/Page column 4, (2010/07/04)

An integrated process is provided for preparing 2,3,5,6-tetraminotoluene and salts thereof starting with nitration of 2,6-dihalotoluene. The process design eliminates costly intermediate drying and recrystallization steps. Handling of solid materials with

PROCESS FOR THE SYNTHESIS OF DIHALODINITROTOLUENE

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Page/Page column 3-4, (2010/07/04)

An improved process is provided for the preparation of 2,6-dihalo-3,5-dinitrotoluene by the nitration of 2,6-dihalotoluene. The direct isolation of highly pure 2,6-dihalo-3,5-dinitrotoluene is accomplished without a water or ice quench, by providing at le

INTEGRATED PROCESS FOR THE PREPARATION OF POLYBENZIMIDAZOLE PRECURSORS

-

Page/Page column 6, (2010/07/04)

An integrated process is provided for preparing complexes of 2,3,5,6-tetraminotoluene with an aromatic diacid starting with nitration of 2,6-dihalotoluene. The process design eliminates costly intermediate drying and recrystallization steps. Handling of s

Quinolonecarboxylic acid derivatives and their preparation

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, (2008/06/13)

Quinolonecarboxylic acid derivatives of the following formula, STR1 wherein R indicates straight or branched lower alkyl, R1 indicates cycloalkyl having 3 to 6 carbon atoms, straight or branched lower alkyl, halogenoalkyl, alkenyl, hydroxyalkyl

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