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1312012-07-9

C15H13BrN4O3S is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1312012-07-9 Structure

  • Basic information

    1. Product Name: C15H13BrN4O3S
    2. Synonyms:
    3. CAS NO:1312012-07-9
    4. Molecular Formula:
    5. Molecular Weight: 409.263
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1312012-07-9.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: C15H13BrN4O3S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C15H13BrN4O3S(1312012-07-9)
    11. EPA Substance Registry System: C15H13BrN4O3S(1312012-07-9)

  • 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: 1312012-07-9(Hazardous Substances Data)

1312012-07-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1312012-07-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,2,0,1 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1312012-07:
(9*1)+(8*3)+(7*1)+(6*2)+(5*0)+(4*1)+(3*2)+(2*0)+(1*7)=69
69 % 10 = 9
So 1312012-07-9 is a valid CAS Registry Number.

1312012-07-9Downstream Products

1312012-07-9Relevant articles and documents

Orally active aminopyridines as inhibitors of tetrameric fructose-1,6-bisphosphatase

Hebeisen, Paul,Haap, Wolfgang,Kuhn, Bernd,Mohr, Peter,Wessel, Hans Peter,Zutter, Ulrich,Kirchner, Stephan,Ruf, Armin,Benz, J?rg,Joseph, Catherine,Alvarez-Sánchez, Rubén,Gubler, Marcel,Schott, Brigitte,Benardeau, Agnes,Tozzo, Effie,Kitas, Eric

, p. 3237 - 3242 (2011/07/07)

A novel sulfonylureido pyridine series exemplified by compound 19 yielded potent inhibitors of FBPase showing significant glucose reduction and modest glycogen lowering in the acute db/db mouse model for Type-2 diabetes. Our inhibitors occupy the allosteric binding site and also extend into the dyad interface region of tetrameric FBPase.

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