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CAS

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91084-99-0

3-(ethylenedioxy)-2-(p-tolylsulfinylmethyl)-7,7-dimethylbicyclo<3.3.0>octane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 91084-99-0 Structure

  • Basic information

    1. Product Name: 3-(ethylenedioxy)-2-(p-tolylsulfinylmethyl)-7,7-dimethylbicyclo<3.3.0>octane
    2. Synonyms: 3-(ethylenedioxy)-2-(p-tolylsulfinylmethyl)-7,7-dimethylbicyclo<3.3.0>octane
    3. CAS NO:91084-99-0
    4. Molecular Formula:
    5. Molecular Weight: 364.506
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 91084-99-0.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: 3-(ethylenedioxy)-2-(p-tolylsulfinylmethyl)-7,7-dimethylbicyclo<3.3.0>octane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(ethylenedioxy)-2-(p-tolylsulfinylmethyl)-7,7-dimethylbicyclo<3.3.0>octane(91084-99-0)
    11. EPA Substance Registry System: 3-(ethylenedioxy)-2-(p-tolylsulfinylmethyl)-7,7-dimethylbicyclo<3.3.0>octane(91084-99-0)

  • 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: 91084-99-0(Hazardous Substances Data)

91084-99-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91084-99-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,0,8 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 91084-99:
(7*9)+(6*1)+(5*0)+(4*8)+(3*4)+(2*9)+(1*9)=140
140 % 10 = 0
So 91084-99-0 is a valid CAS Registry Number.

91084-99-0Downstream Products

91084-99-0Relevant articles and documents

SYNTHESIS OF dl-PENTALENOLACTONES E AND F.

Cane,Thomas

, p. 5295 - 5303 (1984)

The methyl esters of ( plus or minus )-pentalenolactone E and F have been synthesized by a route based on the intramolecular insertion of an alpha -acylcarbene into an unactivated C-H bond to effect closure of the key fused delta -lactone ring system. Lactone reduction, deketalization, and selective acetalization of the derived lactol provided as a mixture of epimers.

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