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87578-92-5

8-acetoxy-t-4-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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  • 87578-92-5 Structure

  • Basic information

    1. Product Name: 8-acetoxy-t-4-p-menth-1-en-7-ol
    2. Synonyms: 8-acetoxy-t-4-p-menth-1-en-7-ol
    3. CAS NO:87578-92-5
    4. Molecular Formula:
    5. Molecular Weight: 212.289
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 87578-92-5.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: 8-acetoxy-t-4-p-menth-1-en-7-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 8-acetoxy-t-4-p-menth-1-en-7-ol(87578-92-5)
    11. EPA Substance Registry System: 8-acetoxy-t-4-p-menth-1-en-7-ol(87578-92-5)

  • 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: 87578-92-5(Hazardous Substances Data)

87578-92-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87578-92-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,5,7 and 8 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 87578-92:
(7*8)+(6*7)+(5*5)+(4*7)+(3*8)+(2*9)+(1*2)=195
195 % 10 = 5
So 87578-92-5 is a valid CAS Registry Number.

87578-92-5Upstream product

87578-92-5Downstream Products

87578-92-5Relevant articles and documents

THE STEREOSPECIFIC HYDROXILATION OF ENDOCYCLIC ETHYLENIC LINKAGE IN THE BIOTRANSFORMATION OF α- TERPINYL ACETATE WITH CULTURED SUSPENSION CELLS OF NICOTIANA TABACUM

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

, p. 671 - 674 (1982)

The biotransformation of (+/-)-8-acetoxy-p-menth-1-ene (α-terpinyl acetate) with the cultured cells of Nicotiana tabacum was found to result in the predominant formation of 8-acetoxy-c-4-p-menthane-r-1, t-2-diol.This experimental result indicates that the hydroxylation of the endocyclic ethylenic linkage with the cultured suspension cells is stereospecific.

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