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CAS

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124908-82-3

2-chloro-3-phenyl-1-cyclobuten-1-yl-acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 124908-82-3 Structure

  • Basic information

    1. Product Name: 2-chloro-3-phenyl-1-cyclobuten-1-yl-acetate
    2. Synonyms:
    3. CAS NO:124908-82-3
    4. Molecular Formula:
    5. Molecular Weight: 222.671
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 124908-82-3.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: 2-chloro-3-phenyl-1-cyclobuten-1-yl-acetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-chloro-3-phenyl-1-cyclobuten-1-yl-acetate(124908-82-3)
    11. EPA Substance Registry System: 2-chloro-3-phenyl-1-cyclobuten-1-yl-acetate(124908-82-3)

  • 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: 124908-82-3(Hazardous Substances Data)

124908-82-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 124908-82-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,9,0 and 8 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 124908-82:
(8*1)+(7*2)+(6*4)+(5*9)+(4*0)+(3*8)+(2*8)+(1*2)=133
133 % 10 = 3
So 124908-82-3 is a valid CAS Registry Number.

124908-82-3Relevant articles and documents

A NEW TWO-CARBON OLEFIN HOMOLOGATION PROCEDURE THAT LEADS TO α-CHLOROENONES. AN EFFICIENT SYNTHESIS OF d,l-MUSCONE

Depres, Jean-Pierre,Navarro, Brigitte,Greene, Andrew E.

, p. 2989 - 2998 (1989)

Dichloroketene-olefin cycloadducts, α,α-dichlorocyclobutanones, are easily converted to α-chloroenones through a 3-step (2-pot) sequence of reactions.The overall result is the insertion of a functionalized 2-carbon unit between the original olefinic carbons.The efficiency of the method is demonstrated by a high-yield synthesis of d,l-muscone.

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