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2,6-dichloro-1-nitrobenzoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

69708-32-3

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69708-32-3 Usage

Chemical compound

2,6-dichloro-1-nitrobenzoic acid

Physical properties

yellow crystalline powder

Uses

synthesis of pharmaceuticals and organic compounds, production of dyes and pigments

Hazards

can be hazardous if ingested, inhaled, or in contact with skin

Industrial applications

versatile chemical with various industrial uses

Check Digit Verification of cas no

The CAS Registry Mumber 69708-32-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,7,0 and 8 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 69708-32:
(7*6)+(6*9)+(5*7)+(4*0)+(3*8)+(2*3)+(1*2)=163
163 % 10 = 3
So 69708-32-3 is a valid CAS Registry Number.

69708-32-3Upstream product

69708-32-3Relevant academic research and scientific papers

Method for synthesizing BTAHNAB by taking 3, 5-dichlorobenzoic acid as raw material

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Paragraph 0017; 0019; 0024-0027, (2020/11/09)

The invention belongs to the technical field of organic energetic materials and preparation methods thereof, and provides a method for synthesizing a novel heat-resistant energetic material BTAHNAB bytaking 3, 5-dichlorobenzoic acid as a raw material. The method comprises the following steps of: adding 3, 5-dichlorobenzoic acid into nitro-sulfuric acid, and carrying out reaction to obtain 3, 5-dichloro-4-nitrobenzoic acid; adding the 3, 5-dichloro-4-nitrobenzoic acid into sulfuric acid, dropwise adding chloroform, adding sodium azide, and carrying out reaction to obtain 3, 5-dichloro-4-nitroaniline; sequentially adding sodium nitrate and 3, 5-dichloro-4-nitroaniline into sulfuric acid, and carrying out reaction to obtain 3, 3', 5, 5'-tetrachloro-2, 2', 4, 4', 6, 6'-hexanitroazobenzene; performing mixing with toluene, introducing ammonia gas at a constant speed, stopping introducing the ammonia gas at the end of the reaction, and continuously carrying out reaction to obtain the BTAHNAB. Through calculation and test analysis, the detonation velocity of the final product exceeds 8000m/s, the melting point is larger than 330DEG C, the thermal decomposition temperature is close to 400DEG C, and the final product has good stability and thermal stability, and is a novel heat-resistant explosive with wide application prospects.

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