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C37H32N4O4 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1312939-15-3 Structure
  • Basic information

    1. Product Name: C37H32N4O4
    2. Synonyms: C37H32N4O4
    3. CAS NO:1312939-15-3
    4. Molecular Formula:
    5. Molecular Weight: 596.685
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1312939-15-3.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: C37H32N4O4(CAS DataBase Reference)
    10. NIST Chemistry Reference: C37H32N4O4(1312939-15-3)
    11. EPA Substance Registry System: C37H32N4O4(1312939-15-3)
  • 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: 1312939-15-3(Hazardous Substances Data)

1312939-15-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1312939-15-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,2,9,3 and 9 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1312939-15:
(9*1)+(8*3)+(7*1)+(6*2)+(5*9)+(4*3)+(3*9)+(2*1)+(1*5)=143
143 % 10 = 3
So 1312939-15-3 is a valid CAS Registry Number.

1312939-15-3Downstream Products

1312939-15-3Relevant articles and documents

Synthesis and evaluation of indole-based new scaffolds for antimicrobial activities - Identification of promising candidates

Singh, Palwinder,Verma, Puja,Yadav, Bhawna,Komath, Sneha S.

, p. 3367 - 3372 (2011)

Search for new antimicrobial agents led to the synthesis of series of N-1, C-3 and C-5 substituted bis-indoles. Their evaluation for antifungal and antibacterial activities resulted in the optimization of pyrrolidine/morpholine/ N-benzyl moiety at the C-3 end and propane/butane/xylidine groups as linkers between two indoles for significant inhibition of microbial growth. Preliminary investigations have identified three highly potent antimicrobial agents. Dockings of these molecules in the active sites of lanosterol demethylase, dihydrofolate reductase and topoisomerase II indicate their strong interactions with these enzymes.

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