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4-iodo-N-(2-pyridinylmethyl)benzenesulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 433964-89-7 Structure
  • Basic information

    1. Product Name: 4-iodo-N-(2-pyridinylmethyl)benzenesulfonamide
    2. Synonyms: 4-iodo-N-(2-pyridinylmethyl)benzenesulfonamide
    3. CAS NO:433964-89-7
    4. Molecular Formula: C12H11IN2O2S
    5. Molecular Weight: 374.19741
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 433964-89-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-iodo-N-(2-pyridinylmethyl)benzenesulfonamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-iodo-N-(2-pyridinylmethyl)benzenesulfonamide(433964-89-7)
    11. EPA Substance Registry System: 4-iodo-N-(2-pyridinylmethyl)benzenesulfonamide(433964-89-7)
  • 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: 433964-89-7(Hazardous Substances Data)

433964-89-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 433964-89-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,3,9,6 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 433964-89:
(8*4)+(7*3)+(6*3)+(5*9)+(4*6)+(3*4)+(2*8)+(1*9)=177
177 % 10 = 7
So 433964-89-7 is a valid CAS Registry Number.

433964-89-7Upstream product

433964-89-7Downstream Products

433964-89-7Relevant articles and documents

PYRIMIDINE COMPOUNDS

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Page/Page column 52, (2008/06/13)

Compounds of the formula (I), wherein R1, R2, R3, R4, R5 and p are as defined within and a pharmaceutically acceptable salts and in vivo hydrolysable esters are described. Also described are processes

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