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1375479-13-2

C15H10I2O is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1375479-13-2 Structure

  • Basic information

    1. Product Name: C15H10I2O
    2. Synonyms: C15H10I2O
    3. CAS NO:1375479-13-2
    4. Molecular Formula:
    5. Molecular Weight: 460.053
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1375479-13-2.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: C15H10I2O(CAS DataBase Reference)
    10. NIST Chemistry Reference: C15H10I2O(1375479-13-2)
    11. EPA Substance Registry System: C15H10I2O(1375479-13-2)

  • 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: 1375479-13-2(Hazardous Substances Data)

1375479-13-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1375479-13-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,5,4,7 and 9 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1375479-13:
(9*1)+(8*3)+(7*7)+(6*5)+(5*4)+(4*7)+(3*9)+(2*1)+(1*3)=192
192 % 10 = 2
So 1375479-13-2 is a valid CAS Registry Number.

1375479-13-2Downstream Products

1375479-13-2Relevant articles and documents

Catalytic generation of arynes and trapping by nucleophilic addition and iodination

Hamura, Toshiyuki,Chuda, Yu,Nakatsuji, Yuya,Suzuki, Keisuke

supporting information; experimental part, p. 3368 - 3372 (2012/06/18)

A fair exchange: In the title reaction, alkynyllithium serves as an initiator for benzyne generation through an iodine-lithium exchange (see scheme; Tf=trifluoromethanesulfonyl). When performed in the presence of stoichiometric amounts of a nucleophile, the generated benzyne undergoes attack by lithio nucleophiles to generate aryllithium, which is then iodinated by iodoalkyne to give the iodoarenes 1. Copyright

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