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TM-trans-carveol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 81517-75-1 Structure
  • Basic information

    1. Product Name: TM-trans-carveol
    2. Synonyms: TM-trans-carveol
    3. CAS NO:81517-75-1
    4. Molecular Formula:
    5. Molecular Weight: 208.344
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 81517-75-1.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: TM-trans-carveol(CAS DataBase Reference)
    10. NIST Chemistry Reference: TM-trans-carveol(81517-75-1)
    11. EPA Substance Registry System: TM-trans-carveol(81517-75-1)
  • 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: 81517-75-1(Hazardous Substances Data)

81517-75-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81517-75-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,5,1 and 7 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 81517-75:
(7*8)+(6*1)+(5*5)+(4*1)+(3*7)+(2*7)+(1*5)=131
131 % 10 = 1
So 81517-75-1 is a valid CAS Registry Number.

81517-75-1Relevant articles and documents

OXYGENATED LIMONENE ANALOGS. PREPARATION OF TETRAMETHYLATED CARVONE AND CARVEOLS VIA REGIOCONTROLLED OPENING OF TETRAMETHYLLIMONENE OXIDE.

Giguere, Raymond J.,Hoffmann, H. M. R.

, p. 5039 - 5042 (1981)

Regioselective opening of trans epoxide 2 gave endo and exo tetramethylated trans carveols 3t and 4t, respectively, which were oxidized to tetramethylcarvone (5) and its unstable exocyclic isomer 6; reduction of 5 with DIBAH gave tetramethylated cis carve

Homologues of Monocyclic Monoterpenes. Tetramethylated Derivatives of Carvone, Carveol, β-Terpineol, Sobrerol, and Related Compounds

Giguere, Raymond J.,Ilsemann, Godard von,Hoffmann, H. M. R.

, p. 4948 - 4954 (2007/10/02)

Epoxidation of tetramethyllimonene (1) gave monoepoxide 2t, which was opened regioselectively to endo and exo tetramethylated trans-carveols 3t and 5t, respectively.The alcohols were further oxidized to tetramethylcarvone (4) and its unstable exocyclic is

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