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CAS

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127716-99-8

(1S,2R,3S)-2,3-Dimethyl-2-vinyl-cyclohexanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 127716-99-8 Structure

  • Basic information

    1. Product Name: (1S,2R,3S)-2,3-Dimethyl-2-vinyl-cyclohexanol
    2. Synonyms:
    3. CAS NO:127716-99-8
    4. Molecular Formula:
    5. Molecular Weight: 154.252
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 127716-99-8.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: (1S,2R,3S)-2,3-Dimethyl-2-vinyl-cyclohexanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1S,2R,3S)-2,3-Dimethyl-2-vinyl-cyclohexanol(127716-99-8)
    11. EPA Substance Registry System: (1S,2R,3S)-2,3-Dimethyl-2-vinyl-cyclohexanol(127716-99-8)

  • 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: 127716-99-8(Hazardous Substances Data)

127716-99-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 127716-99-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,7,1 and 6 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 127716-99:
(8*1)+(7*2)+(6*7)+(5*7)+(4*1)+(3*6)+(2*9)+(1*9)=148
148 % 10 = 8
So 127716-99-8 is a valid CAS Registry Number.

127716-99-8Relevant articles and documents

STEREOSELECTIVE CYCLIZATION OF (E)- AND (Z)-5,6-DIMETHYL-8-TRIMETHYLSILYL-6-OCTENALS

Asao, Kazuhiko,Iio, Hideo,Tokoroyama, Takashi

, p. 6397 - 6400 (2007/10/02)

The diastereoselectivities in the acid-mediated cyclization of (E)- and (Z)-5,6-dimethyl-8-trimethylsilyl-6-octenals, both stereoselectively synthesized, were investigated.Excellent preference for the formation of cis-dimethylcyclohexanols was realized, s

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