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2,4-Dibromo-6-methyl-3-nitroaniline is a chemical compound characterized by its molecular formula C7H6Br2N2O2. It is a yellow solid with a molecular weight of 306.94 g/mol. 2,4-Dibromo-6-methyl-3-nitroaniline is known for its use in the synthesis of various organic compounds and possesses herbicidal properties. Due to its potential hazards, it requires careful handling, proper storage in a cool, dry place away from ignition sources, and regulated disposal.

117824-53-0

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117824-53-0 Usage

Uses

Used in Organic Synthesis:
2,4-Dibromo-6-methyl-3-nitroaniline is used as a synthetic intermediate for the production of various organic compounds. Its unique structure allows it to be a valuable building block in the creation of a wide range of chemical products.
Used in Herbicide Formulation:
In the agricultural industry, 2,4-Dibromo-6-methyl-3-nitroaniline is used as an active ingredient in herbicide formulations. Its herbicidal properties make it effective in controlling the growth of unwanted plants, thereby enhancing crop productivity and yield.
Safety Precautions:
When handling 2,4-Dibromo-6-methyl-3-nitroaniline, it is crucial to take necessary safety measures to prevent skin contact and inhalation, as it can be harmful. Proper storage and disposal according to local regulations are also essential to minimize environmental and health risks.

Check Digit Verification of cas no

The CAS Registry Mumber 117824-53-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,8,2 and 4 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 117824-53:
(8*1)+(7*1)+(6*7)+(5*8)+(4*2)+(3*4)+(2*5)+(1*3)=130
130 % 10 = 0
So 117824-53-0 is a valid CAS Registry Number.

117824-53-0Upstream product

117824-53-0Relevant articles and documents

Synthesis of Indoles via Ring Closure of 2-Alkylnitroaniline Derivatives.

Bergman, Jan,Sand, Peter

, p. 6085 - 6112 (2007/10/02)

A variety of nitroindoles have been prepared from imidate, amidine, and sec-anilide derivatives of 2-alkyl-3- or 5-nitroanilines by a base-induced cyclization promoted by dialkyl oxalates.It is shown that essentially the same procedure also can be used to synthesize the corresponding nitroindole-3-glyoxylates in one simple operation.The synthetic potential is discussed and a mechanism is proposed.

Halogenation Using Quaternary Ammonium Polyhalides. VI. Bromination of Aromatic Amines by Use of Benzyltrimethylammonium Tribromide

Kajigaeshi, Shoji,Kakinami, Takaaki,Inoue, Kazuhisa,Kondo, Manabu,Nakamura, Hiroko,et al.

, p. 597 - 599 (2007/10/02)

The reaction of aromatic amines with benzyltrimethylammonium tribromide in dichloromethane-methanol containing calcium carbonate powder for 0.5 h at room temperature gave bromo-substituted aromatic amines in good yields.

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