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103189-88-4

2,6-dimethyl-2-(prop-2-enyl)cyclohexanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 103189-88-4 Structure

  • Basic information

    1. Product Name: 2,6-dimethyl-2-(prop-2-enyl)cyclohexanone
    2. Synonyms:
    3. CAS NO:103189-88-4
    4. Molecular Formula:
    5. Molecular Weight: 166.263
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 103189-88-4.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: 2,6-dimethyl-2-(prop-2-enyl)cyclohexanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,6-dimethyl-2-(prop-2-enyl)cyclohexanone(103189-88-4)
    11. EPA Substance Registry System: 2,6-dimethyl-2-(prop-2-enyl)cyclohexanone(103189-88-4)

  • 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: 103189-88-4(Hazardous Substances Data)

103189-88-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103189-88-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,1,8 and 9 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 103189-88:
(8*1)+(7*0)+(6*3)+(5*1)+(4*8)+(3*9)+(2*8)+(1*8)=114
114 % 10 = 4
So 103189-88-4 is a valid CAS Registry Number.

103189-88-4Downstream Products

103189-88-4Relevant articles and documents

ASYMMETRIC DEPROTONATION OF PROCHIRAL KETONES USING CHIRAL LITHIUM AMIDE BASES

Cain, Christian M.,Cousins, Richard P. C.,Coumbarides, Greg,Simpkins, Nigel S.

, p. 523 - 544 (1990)

A number of chiral secondary amines have been prepared and used as precursors to the corresponding chiral lithium amide bases.Treatment of either cis-2,6-dimethylcyclohexanone or 4-tert-butylcyclohexanone with a chiral lithium amide, followed by electrophilic quench, gives chiral products in up to 88 percent enantiomeric excess.The results with 4-tert-butylcyclohexanone are in disagreement with an earlier literature report, giving products of lower enantiomeric excess but higher optical rotation.

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