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CAS

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403641-44-1

Ethanone, 1-[(1R,2S)-2-(1-methylethyl)cyclohexyl]- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 403641-44-1 Structure

  • Basic information

    1. Product Name: Ethanone, 1-[(1R,2S)-2-(1-methylethyl)cyclohexyl]- (9CI)
    2. Synonyms: Ethanone, 1-[(1R,2S)-2-(1-methylethyl)cyclohexyl]- (9CI)
    3. CAS NO:403641-44-1
    4. Molecular Formula: C11H20O
    5. Molecular Weight: 168.2759
    6. EINECS: N/A
    7. Product Categories: ISOPROPYL;ACETYLGROUP
    8. Mol File: 403641-44-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Ethanone, 1-[(1R,2S)-2-(1-methylethyl)cyclohexyl]- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Ethanone, 1-[(1R,2S)-2-(1-methylethyl)cyclohexyl]- (9CI)(403641-44-1)
    11. EPA Substance Registry System: Ethanone, 1-[(1R,2S)-2-(1-methylethyl)cyclohexyl]- (9CI)(403641-44-1)

  • 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: 403641-44-1(Hazardous Substances Data)

403641-44-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 403641-44-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,3,6,4 and 1 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 403641-44:
(8*4)+(7*0)+(6*3)+(5*6)+(4*4)+(3*1)+(2*4)+(1*4)=111
111 % 10 = 1
So 403641-44-1 is a valid CAS Registry Number.

403641-44-1Downstream Products

403641-44-1Relevant articles and documents

Cu-catalyzed asymmetric conjugate additions of alkylzinc reagents to acyclic aliphatic enones

Mizutani, Hirotake,Degrado, Sylvia J.,Hoveyda, Amir H.

, p. 779 - 781 (2007/10/03)

Cu-catalyzed enantioselective conjugate additions to acyclic aliphatic enones are reported. The resulting enolates may be functionalized intra- and intermolecularly, leading to the formation of an additional C-C bond. The utility of the present method is not limited to reactions involving Et2Zn; a variety of alkylzincs may be used. Moreover, many of the requisite substrates can be easily accessed through catalytic olefin cross metathesis. Copyright

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