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84072-07-1

2-Cyclohexene-1-methanol, 5-hydroxy-2,6,6-trimethyl-, a-acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 2-Cyclohexene-1-methanol, 5-hydroxy-2,6,6-trimethyl-, a-acetate

    Cas No: 84072-07-1

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  • 84072-07-1 Structure

  • Basic information

    1. Product Name: 2-Cyclohexene-1-methanol, 5-hydroxy-2,6,6-trimethyl-, a-acetate
    2. Synonyms:
    3. CAS NO:84072-07-1
    4. Molecular Formula: C12H20O3
    5. Molecular Weight: 212.289
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 84072-07-1.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: 2-Cyclohexene-1-methanol, 5-hydroxy-2,6,6-trimethyl-, a-acetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Cyclohexene-1-methanol, 5-hydroxy-2,6,6-trimethyl-, a-acetate(84072-07-1)
    11. EPA Substance Registry System: 2-Cyclohexene-1-methanol, 5-hydroxy-2,6,6-trimethyl-, a-acetate(84072-07-1)

  • 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: 84072-07-1(Hazardous Substances Data)

84072-07-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84072-07-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,0,7 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 84072-07:
(7*8)+(6*4)+(5*0)+(4*7)+(3*2)+(2*0)+(1*7)=121
121 % 10 = 1
So 84072-07-1 is a valid CAS Registry Number.

84072-07-1Downstream Products

84072-07-1Relevant articles and documents

Stereo- and regio-selective Ti-mediated radical cyclization of epoxy-alkenes: Synthesis of the A and C ring synthons of paclitaxel

Nakai, Kazuoki,Kamoshita, Miyuki,Doi, Takayuki,Yamada, Haruo,Takahashi, Takashi

, p. 7855 - 7857 (2001)

We have developed a practical synthetic route for the A and C rings of paclitaxel. The key reaction is a Ti-mediated radical cyclization of an epoxyalkene.

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