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CAS

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103150-27-2

exo-6-chloro-endo-6-phenyl-cis-bicyclo<3.2.0>heptan-7-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 103150-27-2 Structure

  • Basic information

    1. Product Name: exo-6-chloro-endo-6-phenyl-cis-bicyclo<3.2.0>heptan-7-one
    2. Synonyms:
    3. CAS NO:103150-27-2
    4. Molecular Formula:
    5. Molecular Weight: 220.699
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 103150-27-2.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: exo-6-chloro-endo-6-phenyl-cis-bicyclo<3.2.0>heptan-7-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: exo-6-chloro-endo-6-phenyl-cis-bicyclo<3.2.0>heptan-7-one(103150-27-2)
    11. EPA Substance Registry System: exo-6-chloro-endo-6-phenyl-cis-bicyclo<3.2.0>heptan-7-one(103150-27-2)

  • 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: 103150-27-2(Hazardous Substances Data)

103150-27-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103150-27-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,1,5 and 0 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 103150-27:
(8*1)+(7*0)+(6*3)+(5*1)+(4*5)+(3*0)+(2*2)+(1*7)=62
62 % 10 = 2
So 103150-27-2 is a valid CAS Registry Number.

103150-27-2Downstream Products

103150-27-2Relevant articles and documents

Allylic Displacements and a Novel Ester-Ether Interchange in Fused Cyclobutanones

Hassner, Alfred,Dillon, John

, p. 3315 - 3319 (1986)

Chlorophenylcyclobutanone 11, prepared by chlorophenylketene addition to cyclohexene, reacts readily with simple and hindered carboxylic acids in a cine substitution to produce keto esters 14.The acyloxy and phenyl substituents in 14c are shown by X-ray diffraction to be cis oriented; nevertheless 14 reacts with NaOMe at 20 deg C by an unusual ester-ether interchange to produce 15 and the released carboxylate RCO2-.These reactions apparently proceed via an oxyallyl cation intermediate.The behaviors of related cyclobutanones 4, 6, and 11 with methoxide are contrasted.

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