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Bis(3,5-dichloro-2,4,6-trinitrophenyl)-diazene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 116763-58-7 Structure
  • Basic information

    1. Product Name: Bis(3,5-dichloro-2,4,6-trinitrophenyl)-diazene
    2. Synonyms: Bis(3,5-dichloro-2,4,6-trinitrophenyl)-diazene
    3. CAS NO:116763-58-7
    4. Molecular Formula: C12Cl4N8O12
    5. Molecular Weight: 589.9868
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 116763-58-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 804.2°C at 760 mmHg
    3. Flash Point: 440.2°C
    4. Appearance: /
    5. Density: 2.38g/cm3
    6. Vapor Pressure: 6.93E-25mmHg at 25°C
    7. Refractive Index: 1.858
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: Bis(3,5-dichloro-2,4,6-trinitrophenyl)-diazene(CAS DataBase Reference)
    11. NIST Chemistry Reference: Bis(3,5-dichloro-2,4,6-trinitrophenyl)-diazene(116763-58-7)
    12. EPA Substance Registry System: Bis(3,5-dichloro-2,4,6-trinitrophenyl)-diazene(116763-58-7)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 116763-58-7(Hazardous Substances Data)

116763-58-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 116763-58-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,7,6 and 3 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 116763-58:
(8*1)+(7*1)+(6*6)+(5*7)+(4*6)+(3*3)+(2*5)+(1*8)=137
137 % 10 = 7
So 116763-58-7 is a valid CAS Registry Number.
InChI:InChI=1/C12Cl4N8O12/c13-1-7(19(25)26)2(14)10(22(31)32)5(9(1)21(29)30)17-18-6-11(23(33)34)3(15)8(20(27)28)4(16)12(6)24(35)36

116763-58-7Downstream Products

116763-58-7Relevant articles and documents

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

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Paragraph 0015-0016; 0018-0026, (2020/11/02)

The invention belongs to the technical field of organic energetic materials and preparation thereof, and provides a method for synthesizing a novel heat-resistant energetic material 3, 3 ', 5, 5'-tetraamino-2, 2 ', 4, 4', 6, 6 '-hexanitroazobenzene (BTAHNAB) by taking 3, 5-dichloroaniline as a raw material. The method comprises the following steps: adding 3. 5-dichloroaniline into a nitro-sulfur mixed acid, and reacting to obtain 3, 3', 5, 5 '-tetrachloro-2, 2', 4, 4 ', 6, 6'-hexanitroazobenzene; then mixing with methylbenzene, introducing ammonia gas at a constant speed, stopping introducingthe ammonia gas after reaction, and continuously reacting to obtain the BTAHNAB. The preparation process is safe and simple, the preparation period is short, the preparation steps are few, and the preparation yield is high. Through calculation and test analysis, the detonation velocity of the BTAHNAB exceeds 8000m/s, the melting point of the BTAHNAB is greater than 330 DEG C, and the thermal decomposition temperature of the BTAHNAB is close to 400 DEG C, so that the obtained product has good stability and thermal stability, and is a novel heat-resistant explosive with a wide application prospect.

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

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, (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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