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  • 1380111-09-0 Structure
  • Basic information

    1. Product Name: C12H15NO3
    2. Synonyms: C12H15NO3
    3. CAS NO:1380111-09-0
    4. Molecular Formula:
    5. Molecular Weight: 221.256
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1380111-09-0.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: C12H15NO3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C12H15NO3(1380111-09-0)
    11. EPA Substance Registry System: C12H15NO3(1380111-09-0)
  • 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: 1380111-09-0(Hazardous Substances Data)

1380111-09-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1380111-09-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,0,1,1 and 1 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1380111-09:
(9*1)+(8*3)+(7*8)+(6*0)+(5*1)+(4*1)+(3*1)+(2*0)+(1*9)=110
110 % 10 = 0
So 1380111-09-0 is a valid CAS Registry Number.

1380111-09-0Relevant articles and documents

Pyridone-conjugated monobactam antibiotics with gram-negative activity

Brown, Matthew F.,Mitton-Fry, Mark J.,Arcari, Joel T.,Barham, Rose,Casavant, Jeffrey,Gerstenberger, Brian S.,Han, Seungil,Hardink, Joel R.,Harris, Thomas M.,Hoang, Thuy,Huband, Michael D.,Lall, Manjinder S.,Lemmon, M. Megan,Li, Chao,Lin, Jian,McCurdy, Sandra P.,McElroy, Eric,McPherson, Craig,Marr, Eric S.,Mueller, John P.,Mullins, Lisa,Nikitenko, Antonia A.,Noe, Mark C.,Penzien, Joseph,Plummer, Mark S.,Schuff, Brandon P.,Shanmugasundaram, Veerabahu,Starr, Jeremy T.,Sun, Jianmin,Tomaras, Andrew,Young, Jennifer A.,Zaniewski, Richard P.

, p. 5541 - 5552 (2013/07/26)

Herein we describe the structure-aided design and synthesis of a series of pyridone-conjugated monobactam analogues with in vitro antibacterial activity against clinically relevant Gram-negative species including Pseudomonas aeruginosa, Klebsiella pneumoniae, and Escherichia coli. Rat pharmacokinetic studies with compound 17 demonstrate low clearance and low plasma protein binding. In addition, evidence is provided for a number of analogues suggesting that the siderophore receptors PiuA and PirA play a role in drug uptake in P. aeruginosa strain PAO1.

MONOBACTAMS

-

, (2012/06/16)

The present invention is directed to a new class of monobactam derivatives and their use for treating bacterial infections.

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