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1035967-94-2

2-((RS)-2-((R)-4-methylcyclohex-3-enyl)propyl)cyclopent-1-enyl acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1035967-94-2 Structure

  • Basic information

    1. Product Name: 2-((RS)-2-((R)-4-methylcyclohex-3-enyl)propyl)cyclopent-1-enyl acetate
    2. Synonyms:
    3. CAS NO:1035967-94-2
    4. Molecular Formula:
    5. Molecular Weight: 262.392
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1035967-94-2.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: 2-((RS)-2-((R)-4-methylcyclohex-3-enyl)propyl)cyclopent-1-enyl acetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-((RS)-2-((R)-4-methylcyclohex-3-enyl)propyl)cyclopent-1-enyl acetate(1035967-94-2)
    11. EPA Substance Registry System: 2-((RS)-2-((R)-4-methylcyclohex-3-enyl)propyl)cyclopent-1-enyl acetate(1035967-94-2)

  • 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: 1035967-94-2(Hazardous Substances Data)

1035967-94-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1035967-94-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,5,9,6 and 7 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1035967-94:
(9*1)+(8*0)+(7*3)+(6*5)+(5*9)+(4*6)+(3*7)+(2*9)+(1*4)=172
172 % 10 = 2
So 1035967-94-2 is a valid CAS Registry Number.

1035967-94-2Downstream Products

1035967-94-2Relevant articles and documents

Synthesis and olfactory evaluation of all stereoisomers of the fragrance Nectaryl

Brenna, Elisabetta,Fuganti, Claudio,Gatti, Francesco G.,Malpezzi, Luciana,Serra, Stefano

, p. 800 - 807 (2008)

The fragrance Nectaryl 1 was prepared by the radical addition of cyclopentanone to (+)-limonene. All the four stereoisomers of this fragrance were prepared by the enzymatic acetylation of the corresponding alcohols in good de. The absolute configurations have been unambiguously assigned by the chemical correlation and X-ray crystal structure of a dinitrobenzoate derivate. The olfactory evaluation is also reported. The odour perception is mainly related to the configuration at the stereocentre α to the carbonyl group. Chiral protonations of the lithium enolate or the enolester of 1 to give a diastereomeric enriched mixture of 1 are reported.

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