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CAS

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70102-02-2

1,3-di(3,5-xylyl)tricyclo<3.3.1.13,7>decane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 70102-02-2 Structure

  • Basic information

    1. Product Name: 1,3-di(3,5-xylyl)tricyclo<3.3.1.13,7>decane
    2. Synonyms:
    3. CAS NO:70102-02-2
    4. Molecular Formula:
    5. Molecular Weight: 344.54
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 70102-02-2.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: 1,3-di(3,5-xylyl)tricyclo<3.3.1.13,7>decane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,3-di(3,5-xylyl)tricyclo<3.3.1.13,7>decane(70102-02-2)
    11. EPA Substance Registry System: 1,3-di(3,5-xylyl)tricyclo<3.3.1.13,7>decane(70102-02-2)

  • 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: 70102-02-2(Hazardous Substances Data)

70102-02-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70102-02-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,1,0 and 2 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 70102-02:
(7*7)+(6*0)+(5*1)+(4*0)+(3*2)+(2*0)+(1*2)=62
62 % 10 = 2
So 70102-02-2 is a valid CAS Registry Number.

70102-02-2Downstream Products

70102-02-2Relevant articles and documents

Direct Clay-Catalyzed Friedel-Crafts Arylation and Chlorination of the Hydrocarbon Adamantane

Chalais, Stephane,Cornelis, Andre,Gerstmans, Andre,Kolodziejski, Waclaw,Laszlo, Pierre,et al.

, p. 1196 - 1203 (1985)

Multiple chlorinations and arylations at the tertiary positions of adamantane are promoted by FeCl3-doped K10 montmorillonite in CCl4 or in aromatic solvents.The process, remarkably easy implement, can be tailored to selective formation of monosubstituted 1-adamantyl derivatives or 1,3-disubstituted adamantanes.The process achieves alkylation at the meta- and para-positions of toluene leading to a purely statistical distribution and displays no substrate specificity in competition experiments between toluene and benzene.

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