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CAS

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152714-04-0

2-Chloro-3-(4-chloro-phenyl)-cyclobut-2-enone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 152714-04-0 Structure

  • Basic information

    1. Product Name: 2-Chloro-3-(4-chloro-phenyl)-cyclobut-2-enone
    2. Synonyms: 2-Chloro-3-(4-chloro-phenyl)-cyclobut-2-enone
    3. CAS NO:152714-04-0
    4. Molecular Formula:
    5. Molecular Weight: 213.063
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 152714-04-0.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-(4-chloro-phenyl)-cyclobut-2-enone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Chloro-3-(4-chloro-phenyl)-cyclobut-2-enone(152714-04-0)
    11. EPA Substance Registry System: 2-Chloro-3-(4-chloro-phenyl)-cyclobut-2-enone(152714-04-0)

  • 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: 152714-04-0(Hazardous Substances Data)

152714-04-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 152714-04-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,2,7,1 and 4 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 152714-04:
(8*1)+(7*5)+(6*2)+(5*7)+(4*1)+(3*4)+(2*0)+(1*4)=110
110 % 10 = 0
So 152714-04-0 is a valid CAS Registry Number.

152714-04-0Relevant articles and documents

Substituent effects on cyclobutyl and cyclopropylcarbinyl cations

Wiberg, Kenneth B.,Shobe, David,Nelson, Gordon L.

, p. 10645 - 10652 (2007/10/02)

The acetolyses of 3-substituted cyclobutyl tosylates (X = Ar, Cl, and OEt) were examined giving rate constants and product distributions. With the alkyl- and aryl-substituted compounds, the rate-determining step leads to the formation of a bridged cyclobu

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