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CAS

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153861-63-3

ethyl (1-chlorocyclohexyl)-azocarboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 153861-63-3 Structure

  • Basic information

    1. Product Name: ethyl (1-chlorocyclohexyl)-azocarboxylate
    2. Synonyms: ethyl (1-chlorocyclohexyl)-azocarboxylate
    3. CAS NO:153861-63-3
    4. Molecular Formula:
    5. Molecular Weight: 218.683
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 153861-63-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: ethyl (1-chlorocyclohexyl)-azocarboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl (1-chlorocyclohexyl)-azocarboxylate(153861-63-3)
    11. EPA Substance Registry System: ethyl (1-chlorocyclohexyl)-azocarboxylate(153861-63-3)

  • 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: 153861-63-3(Hazardous Substances Data)

153861-63-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 153861-63-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,8,6 and 1 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 153861-63:
(8*1)+(7*5)+(6*3)+(5*8)+(4*6)+(3*1)+(2*6)+(1*3)=143
143 % 10 = 3
So 153861-63-3 is a valid CAS Registry Number.

153861-63-3Downstream Products

153861-63-3Relevant articles and documents

Synthesis of 1,2,4-Triazolium Salts: Reaction of 1-Azo-2-azonia-allene Salts with Nitriles

Amer, A. M.

, p. 431 - 438 (1995)

Alkyl ketone hydrazones 1 are oxidized with tert-butylhypochlorite to give geminal chloro azo compounds 2.These react with SbCl5 to give 1-aza-2-azonia-allene salts 3 as reactive intermediates which are intercepted with nitriles to yield 3H-1,2,4-triazoli

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