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103618-46-8

((1S,6R)-6-Vinyl-cyclohex-3-enyl)-methanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 103618-46-8 Structure

  • Basic information

    1. Product Name: ((1S,6R)-6-Vinyl-cyclohex-3-enyl)-methanol
    2. Synonyms:
    3. CAS NO:103618-46-8
    4. Molecular Formula:
    5. Molecular Weight: 138.21
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 103618-46-8.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,6R)-6-Vinyl-cyclohex-3-enyl)-methanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: ((1S,6R)-6-Vinyl-cyclohex-3-enyl)-methanol(103618-46-8)
    11. EPA Substance Registry System: ((1S,6R)-6-Vinyl-cyclohex-3-enyl)-methanol(103618-46-8)

  • 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: 103618-46-8(Hazardous Substances Data)

103618-46-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103618-46-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,6,1 and 8 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 103618-46:
(8*1)+(7*0)+(6*3)+(5*6)+(4*1)+(3*8)+(2*4)+(1*6)=98
98 % 10 = 8
So 103618-46-8 is a valid CAS Registry Number.

103618-46-8Relevant articles and documents

Enantioselective Reduction of Vicinally Substituted Monocyclic Aldehydes with Horse Liver Alcohol Dehydrogenase; A New Approach to Chiral Alcohols and Aldehydes

Boland, Wilhelm,Niedermeyer, Uwe

, p. 28 - 32 (1987)

Optically active, vicinally substituted monocyclic aldehydes and alcohols can be conveniently prepared by enantioselective reduction of racemic aldehydes by means of horse liver alcohol dehydrogenase (HLADH) under kinetically controlled conditions.

The first total synthesis of (+)-mucosin

Henderson, Alan R.,Stec, Jozef,Owen, David R.,Whitby, Richard J.

supporting information; experimental part, p. 3409 - 3411 (2012/05/20)

The first total synthesis of (+)-mucosin has been completed allowing assignment of the absolute stereochemistry of the natural product. A zirconium induced co-cyclisation was utilised to install the correct stereochemistry of the four contiguous stereocentres around the unusual bicyclo[4.3.0]nonene core.

Studies in iridoid synthesis. Chemoselective transformations of cis-1,2,4,6-tetrahydrophthalic anhydride

Stevens, Anne T.,Bull, James R.,Chibale, Kelly

supporting information; experimental part, p. 586 - 595 (2008/10/09)

In the course of synthetic studies towards the development of diastereoselective routes to secoiridoid aglycones, cis-1,2,4,6- tetrahydrophthalic anhydride was transformed into the corresponding lactone cis-3a,4,7,7a-tetrahydro-3H-isobenzofuran-1-one, whi

Chemoselectivity and unusual internal acetal formation in the synthesis of a glycosidation precursor

Stevens, Anne T.,Bull, James R.,Chibale, Kelly

, p. 3175 - 3179 (2008/09/19)

Chemoselective deprotection of a tert-butyldimethyl (TBS) silyl ether group in the presence of an acetal moiety within an advanced iridoid precursor using scandium trifluoromethane-sulfonate at 25°C unexpectedly leads to internal acetal formation in high

217. Enantioselective Syntheses and Absolute Configurations of Viridiene and Aucantene, Two Constituents of Algae Pheromone Bouquets

Boland, Wilhelm,Niedermeyer, Uwe,Jaenicke, Lothar,Goerisch, Helmut

, p. 2062 - 2073 (2007/10/02)

Viridiene ((+)-6; (+)-(3R,4S)-3-((1Z)-1,3-butadienyl)-4-vinylcyclopentene) and aucantene ((+)-18; (+)-(4R,5R)-4-((1E)-1-propenyl)-5-vinylcyclohexene) are constituents of the pheromone bouquets of several brown algae species.Key synthons to the title compo

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