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CAS

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105996-71-2

(-)-(1S,3S)-(3-hydroxy-2,2-dimethyl-6-methylenecyclohexyl)methyl p-toluenesulfonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 105996-71-2 Structure

  • Basic information

    1. Product Name: (-)-(1S,3S)-(3-hydroxy-2,2-dimethyl-6-methylenecyclohexyl)methyl p-toluenesulfonate
    2. Synonyms: (-)-(1S,3S)-(3-hydroxy-2,2-dimethyl-6-methylenecyclohexyl)methyl p-toluenesulfonate
    3. CAS NO:105996-71-2
    4. Molecular Formula:
    5. Molecular Weight: 324.441
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 105996-71-2.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,3S)-(3-hydroxy-2,2-dimethyl-6-methylenecyclohexyl)methyl p-toluenesulfonate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (-)-(1S,3S)-(3-hydroxy-2,2-dimethyl-6-methylenecyclohexyl)methyl p-toluenesulfonate(105996-71-2)
    11. EPA Substance Registry System: (-)-(1S,3S)-(3-hydroxy-2,2-dimethyl-6-methylenecyclohexyl)methyl p-toluenesulfonate(105996-71-2)

  • 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: 105996-71-2(Hazardous Substances Data)

105996-71-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105996-71-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,9,9 and 6 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 105996-71:
(8*1)+(7*0)+(6*5)+(5*9)+(4*9)+(3*6)+(2*7)+(1*1)=152
152 % 10 = 2
So 105996-71-2 is a valid CAS Registry Number.

105996-71-2Relevant articles and documents

Synthesis of Chiral 3'-Hydroxy-&γ-ionylideneacetic Acids

Yamamoto, Hiroshi,Oritani, Takayuki,Yamashita, Kyohei

, p. 2203 - 2208 (2007/10/02)

Four isomers of chiral 3'-hydroxy-γ-ionylideneacetic acid (3'-hydroxy-γ-acid), acidic metabolites of Cercospora cruenta, were synthesized from (+)-(S)-3-hydroxy-2,2-dimethyl-1-cyclohexanone as the chiral starting material.A -sigmatropic rearrangement

SHYNTHESIS OF (1S,5R)-KARAHANA ETHER AND (1S,5R)-KARAHANA LACTONE. THE OPTICALLY ACTIVE FORMS OF UNIQUE MONOTERPENES WITH A 6-OXABICYCLOOCTANE RING SYSTEM

Mori, Kenji,Mori, Hideto

, p. 5487 - 5494 (2007/10/02)

(1S,5R)-(-)-Karahana ether (8,8-dimethyl-2-methylene-6-oxabicyclooctane) and (1S,5R)-(-)-karahana lactone (8,8-dimethyl-2-methylene-6-oxabicyclooctan-7-one) were synthesized from (S)-3-hydroxy-2,2-dimethylcyclohexanone.The natural karahana lactone was shown to be almost racemic (ca. 1.3 percent e.e.).

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