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1287769-02-1

C13H14INO3 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1287769-02-1 Structure

  • Basic information

    1. Product Name: C13H14INO3
    2. Synonyms: C13H14INO3
    3. CAS NO:1287769-02-1
    4. Molecular Formula:
    5. Molecular Weight: 359.164
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1287769-02-1.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: C13H14INO3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C13H14INO3(1287769-02-1)
    11. EPA Substance Registry System: C13H14INO3(1287769-02-1)

  • 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: 1287769-02-1(Hazardous Substances Data)

1287769-02-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1287769-02-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,8,7,7,6 and 9 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1287769-02:
(9*1)+(8*2)+(7*8)+(6*7)+(5*7)+(4*6)+(3*9)+(2*0)+(1*2)=211
211 % 10 = 1
So 1287769-02-1 is a valid CAS Registry Number.

1287769-02-1Downstream Products

1287769-02-1Relevant articles and documents

Iodocyclization of hydroxylamine derivatives based on the control of oxidative aromatization leading to 2,5-dihydroisoxazoles and isoxazoles

Okitsu, Takashi,Sato, Kana,Potewar, Taterao M.,Wada, Akimori

, p. 3438 - 3449 (2011/06/26)

An efficient method for the synthesis of 2,5-dihydroisoxazoles and isoxazoles using iodocyclization of N-alkoxycarbonyl O-propargylic hydroxylamines has been developed. 2,5-Dihydro-4-iodoisoxazole underwent the cross-coupling reactions without aromatization to afford polyfunctionalized 2,5-dihydroisoxazoles. This process was applied to the preparation of valdecoxib and its 2,5-dihydro-derivative.

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