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83921-03-3

(4R)-8-acetoxy-p-menth-1-en-7-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 83921-03-3 Structure

  • Basic information

    1. Product Name: (4R)-8-acetoxy-p-menth-1-en-7-ol
    2. Synonyms:
    3. CAS NO:83921-03-3
    4. Molecular Formula:
    5. Molecular Weight: 212.289
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 83921-03-3.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: (4R)-8-acetoxy-p-menth-1-en-7-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (4R)-8-acetoxy-p-menth-1-en-7-ol(83921-03-3)
    11. EPA Substance Registry System: (4R)-8-acetoxy-p-menth-1-en-7-ol(83921-03-3)

  • 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: 83921-03-3(Hazardous Substances Data)

83921-03-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83921-03-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,9,2 and 1 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 83921-03:
(7*8)+(6*3)+(5*9)+(4*2)+(3*1)+(2*0)+(1*3)=133
133 % 10 = 3
So 83921-03-3 is a valid CAS Registry Number.

83921-03-3Downstream Products

83921-03-3Relevant articles and documents

THE ENANTIOSELECTIVE BIOTRANSFORMATION OF α-TERPINEOL AND ITS ACETATE WITH THE CULTURED CELLS OF NICOTIANA TABACUM

Suga, Takayuki,Hirata, Toshifumi,Lee, Ym Sook

, p. 1595 - 1598 (1982)

In the biotransformation of the enantiomers of p-ment-1-en-8-ol (α-terpineol) and 8-acetoxy-p-ment-1-ene (α-terpinyl acetate) with the cultured suspension cells of Nicotina tabacum, it was clarified that the cultured cells effected the hydroxylation at the 6-position of (4R)-(+)-enantiomer in preference to the (4S)-(-)-enantiomer, whereas the cells did the hydrolysis of the acetoxyl group and the hydroxylation of the ethylenic linkage of (4S)-(-)-α-terpinyl acetate in preference to the (4R)-(+)-enantiomer.

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