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CAS

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123992-77-8

1-(diazoacetonylidene)-4-tert-butylcyclohexane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 123992-77-8 Structure

  • Basic information

    1. Product Name: 1-(diazoacetonylidene)-4-tert-butylcyclohexane
    2. Synonyms:
    3. CAS NO:123992-77-8
    4. Molecular Formula:
    5. Molecular Weight: 220.315
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 123992-77-8.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: 1-(diazoacetonylidene)-4-tert-butylcyclohexane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(diazoacetonylidene)-4-tert-butylcyclohexane(123992-77-8)
    11. EPA Substance Registry System: 1-(diazoacetonylidene)-4-tert-butylcyclohexane(123992-77-8)

  • 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: 123992-77-8(Hazardous Substances Data)

123992-77-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 123992-77-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,9,9 and 2 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 123992-77:
(8*1)+(7*2)+(6*3)+(5*9)+(4*9)+(3*2)+(2*7)+(1*7)=148
148 % 10 = 8
So 123992-77-8 is a valid CAS Registry Number.

123992-77-8Downstream Products

123992-77-8Relevant articles and documents

A New, General Cyclopentenone Synthesis

Ceccherelli, Paolo,Curini, Massimo,Marcotullio, Maria Carla,Rosati, Ornelio,Wenkert, Ernest

, p. 311 - 315 (2007/10/02)

A new synthesis of cyclopentenones, involving an Rh(II)-catalyzed, intramolecular carbon-hydrogen insertion of diazomethyl ketones derived from α,β-unsaturated acids, is described.

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