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904312-12-5

2-Pyridinecarboxamide, 4-amino-6-ethoxy-5-iodo-N-[[4-(methylsulfonyl)phenyl]methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 904312-12-5 Structure

  • Basic information

    1. Product Name: 2-Pyridinecarboxamide, 4-amino-6-ethoxy-5-iodo-N-[[4-(methylsulfonyl)phenyl]methyl]-
    2. Synonyms:
    3. CAS NO:904312-12-5
    4. Molecular Formula: C16H18IN3O4S
    5. Molecular Weight: 475.307
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 904312-12-5.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: 2-Pyridinecarboxamide, 4-amino-6-ethoxy-5-iodo-N-[[4-(methylsulfonyl)phenyl]methyl]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Pyridinecarboxamide, 4-amino-6-ethoxy-5-iodo-N-[[4-(methylsulfonyl)phenyl]methyl]-(904312-12-5)
    11. EPA Substance Registry System: 2-Pyridinecarboxamide, 4-amino-6-ethoxy-5-iodo-N-[[4-(methylsulfonyl)phenyl]methyl]-(904312-12-5)

  • 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: 904312-12-5(Hazardous Substances Data)

904312-12-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 904312-12-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,4,3,1 and 2 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 904312-12:
(8*9)+(7*0)+(6*4)+(5*3)+(4*1)+(3*2)+(2*1)+(1*2)=125
125 % 10 = 5
So 904312-12-5 is a valid CAS Registry Number.

904312-12-5Relevant articles and documents

Aminopyridine carboxamides as c-Jun N-terminal kinase inhibitors: Targeting the gatekeeper residue and beyond

Liu, Gang,Zhao, Hongyu,Liu, Bo,Xin, Zhili,Liu, Mei,Kosogof, Christi,Szczepankiewicz, Bruce G.,Wang, Sanyi,Clampit, Jill E.,Gum, Rebecca J.,Haasch, Deanna L.,Trevillyan, James M.,Sham, Hing L.

, p. 5723 - 5730 (2007/10/03)

The structure-activity relationships of 5,6-positions of aminopyridine carboxamide-based c-Jun N-terminal Kinase (JNK) inhibitors were explored to expand interaction with the kinase specificity and ribose-binding pockets. The syntheses of analogues and the impact of structural modification on in vitro potency and cellular activity are described.

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