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88717-96-8

Bicyclo[3.2.1]oct-3-en-6-ol, 4,7-dimethyl-, (6-endo,7-exo)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 88717-96-8 Structure

  • Basic information

    1. Product Name: Bicyclo[3.2.1]oct-3-en-6-ol, 4,7-dimethyl-, (6-endo,7-exo)-
    2. Synonyms:
    3. CAS NO:88717-96-8
    4. Molecular Formula: C10H16O
    5. Molecular Weight: 152.236
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 88717-96-8.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: Bicyclo[3.2.1]oct-3-en-6-ol, 4,7-dimethyl-, (6-endo,7-exo)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Bicyclo[3.2.1]oct-3-en-6-ol, 4,7-dimethyl-, (6-endo,7-exo)-(88717-96-8)
    11. EPA Substance Registry System: Bicyclo[3.2.1]oct-3-en-6-ol, 4,7-dimethyl-, (6-endo,7-exo)-(88717-96-8)

  • 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: 88717-96-8(Hazardous Substances Data)

88717-96-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88717-96-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,7,1 and 7 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 88717-96:
(7*8)+(6*8)+(5*7)+(4*1)+(3*7)+(2*9)+(1*6)=188
188 % 10 = 8
So 88717-96-8 is a valid CAS Registry Number.

88717-96-8Downstream Products

88717-96-8Relevant articles and documents

Chemical Tranformation of Terpenoids. V. Acidic Conversions of 10-Hydroxygeraniol and 10-Hydroxynerol Derivatives Leading to Cyclic Monoterpenoids

Kitagawa, Isao,Tsujii, Shinji,Nishikawa, Fumiko,Shibuya, Hirotaka

, p. 2639 - 2651 (2007/10/02)

Acid treatment of 1-O-acetyl-10-hydroxygeraniol (5a), 1-O-methyl-10-hydroxygeraniol (5b), 1-O-acetyl-10-hydroxynerol (6a), and 1-O-methyl-10-hydroxynerol (6b) was investigated under various conditions.It was found that treatment of 5a and 6a with HCOOH gave menth-1-ene-8,9-diol (7), while treatment of 5a, 5b, 6a, or 6b with BF3-etherate in CH2Cl2 furnished two menthofuran-type compounds (9, 10) and two bicyclooct-2-ene derivatives (17, 24).Both 9 and 10 were successfully converted to menthofuran (16) and 17 was converted to a bicyclooctenone derivative (23) which was a key intermediate for a synthesis of juvabione (27).Keywords - geraniol; nerol; 10-hydroxygeraniol; 10-hydroxynerol; 10-hydroxygeraniol derivative; 10-hydroxynerol derivative; uroterpenol; menthofuran; bicyclooct-2-ene derivative

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