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1379596-17-4

C15H25INO2P is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1379596-17-4 Structure

  • Basic information

    1. Product Name: C15H25INO2P
    2. Synonyms: C15H25INO2P
    3. CAS NO:1379596-17-4
    4. Molecular Formula:
    5. Molecular Weight: 409.247
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1379596-17-4.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: C15H25INO2P(CAS DataBase Reference)
    10. NIST Chemistry Reference: C15H25INO2P(1379596-17-4)
    11. EPA Substance Registry System: C15H25INO2P(1379596-17-4)

  • 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: 1379596-17-4(Hazardous Substances Data)

1379596-17-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1379596-17-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,9,5,9 and 6 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1379596-17:
(9*1)+(8*3)+(7*7)+(6*9)+(5*5)+(4*9)+(3*6)+(2*1)+(1*7)=224
224 % 10 = 4
So 1379596-17-4 is a valid CAS Registry Number.

1379596-17-4Relevant articles and documents

An approach to the site-selective deoxygenation of hydroxy groups based on catalytic phosphoramidite transfer

Jordan, Peter A.,Miller, Scott J.

, p. 2907 - 2911 (2012)

Selective: The deoxygenation of simple and complex natural products employing a readily synthesized phosphoramidite and tetrazole catalysts can be executed as a two-step process, without the need to isolate intermediate deoxygenation precursors. Furthermore, a peptide-based tetrazole catalyst controls the site selectivity of deoxyerythromycin synthesis (see scheme), thus overcoming the notorious challenges with unprotected erythromycin A. Copyright

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