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123992-62-1

ethyl (ξ-acetoxy-4β-tert-butyl-1-cyclohexyl)acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 123992-62-1 Structure

  • Basic information

    1. Product Name: ethyl (ξ-acetoxy-4β-tert-butyl-1-cyclohexyl)acetate
    2. Synonyms: ethyl (ξ-acetoxy-4β-tert-butyl-1-cyclohexyl)acetate
    3. CAS NO:123992-62-1
    4. Molecular Formula:
    5. Molecular Weight: 284.396
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 123992-62-1.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 (ξ-acetoxy-4β-tert-butyl-1-cyclohexyl)acetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl (ξ-acetoxy-4β-tert-butyl-1-cyclohexyl)acetate(123992-62-1)
    11. EPA Substance Registry System: ethyl (ξ-acetoxy-4β-tert-butyl-1-cyclohexyl)acetate(123992-62-1)

  • 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: 123992-62-1(Hazardous Substances Data)

123992-62-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 123992-62-1 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, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 123992-62:
(8*1)+(7*2)+(6*3)+(5*9)+(4*9)+(3*2)+(2*6)+(1*2)=141
141 % 10 = 1
So 123992-62-1 is a valid CAS Registry Number.

123992-62-1Relevant 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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