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<2R-<2α(R*),3aβ,4β,7β,7aβ>>-Octahydro-7,8,8-trimethyl-2-(1-phenylethoxy)-4,7-methanobenzothiophen is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

100483-68-9

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  • 100483-68-9 Structure

  • Basic information

    1. Product Name: <2R-<2α(R*),3aβ,4β,7β,7aβ>>-Octahydro-7,8,8-trimethyl-2-(1-phenylethoxy)-4,7-methanobenzothiophen
    2. Synonyms:
    3. CAS NO:100483-68-9
    4. Molecular Formula:
    5. Molecular Weight: 316.508
    6. EINECS: N/A
    7. Product Categories: N/A

  • 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: <2R-<2α(R*),3aβ,4β,7β,7aβ>>-Octahydro-7,8,8-trimethyl-2-(1-phenylethoxy)-4,7-methanobenzothiophen(CAS DataBase Reference)
    10. NIST Chemistry Reference: <2R-<2α(R*),3aβ,4β,7β,7aβ>>-Octahydro-7,8,8-trimethyl-2-(1-phenylethoxy)-4,7-methanobenzothiophen(100483-68-9)
    11. EPA Substance Registry System: <2R-<2α(R*),3aβ,4β,7β,7aβ>>-Octahydro-7,8,8-trimethyl-2-(1-phenylethoxy)-4,7-methanobenzothiophen(100483-68-9)

  • 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: 100483-68-9(Hazardous Substances Data)

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100483-68-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100483-68-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,4,8 and 3 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 100483-68:
(8*1)+(7*0)+(6*0)+(5*4)+(4*8)+(3*3)+(2*6)+(1*8)=89
89 % 10 = 9
So 100483-68-9 is a valid CAS Registry Number.

100483-68-9Downstream Products

100483-68-9Relevant academic research and scientific papers

Carbohydrate-Model Compounds, I. Kinetic and Thermodynamic Effects in Acetal Formation of Enantiomerically Pure Thiolactols

Noe, Christian R.,Knollmueller, Max,Wagner, Ernst,Voellenkle, Horst

, p. 3299 - 3310 (2007/10/02)

The synthesis of the enantiomerically pure thiolactol 1 is described.Depending on reaction conditions either (R)-2 or (S)-2 reacts with preference in acetal formation with racemic 1-phenylethanol (rac-2).

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