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CAS

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1394922-46-3

C30H36O8 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1394922-46-3 Structure

  • Basic information

    1. Product Name: C30H36O8
    2. Synonyms: C30H36O8
    3. CAS NO:1394922-46-3
    4. Molecular Formula:
    5. Molecular Weight: 524.611
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1394922-46-3.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: C30H36O8(CAS DataBase Reference)
    10. NIST Chemistry Reference: C30H36O8(1394922-46-3)
    11. EPA Substance Registry System: C30H36O8(1394922-46-3)

  • 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: 1394922-46-3(Hazardous Substances Data)

1394922-46-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1394922-46-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,4,9,2 and 2 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1394922-46:
(9*1)+(8*3)+(7*9)+(6*4)+(5*9)+(4*2)+(3*2)+(2*4)+(1*6)=193
193 % 10 = 3
So 1394922-46-3 is a valid CAS Registry Number.

1394922-46-3Upstream product

1394922-46-3Downstream Products

1394922-46-3Relevant articles and documents

Deoxygenation/dimerization of sugar derivatives with BF3· Et2O-Et3SiH: Synthesis of a β-isonucleoside

Mukherjee, Subhrangshu,Roy, Biswajit G.,Das, Soumendra N.,Mandal, Sukhendu B.

, p. 4929 - 4932,4 (2012)

Lewis acid-Et3SiH induced deoxygenation of anomeric carbon of sugars generates tetrahydrofuran derivatives, accompanied by hitherto unknown dimeric products. If the reagent addition steps are reversed, tetrahydrofuran derivatives are obtained a

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