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214341-15-8

dimethyl 4-(N,N-dimethylcarbamoylthio)isophthalate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 214341-15-8 Structure

  • Basic information

    1. Product Name: dimethyl 4-(N,N-dimethylcarbamoylthio)isophthalate
    2. Synonyms: dimethyl 4-(N,N-dimethylcarbamoylthio)isophthalate
    3. CAS NO:214341-15-8
    4. Molecular Formula:
    5. Molecular Weight: 297.332
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 214341-15-8.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: dimethyl 4-(N,N-dimethylcarbamoylthio)isophthalate(CAS DataBase Reference)
    10. NIST Chemistry Reference: dimethyl 4-(N,N-dimethylcarbamoylthio)isophthalate(214341-15-8)
    11. EPA Substance Registry System: dimethyl 4-(N,N-dimethylcarbamoylthio)isophthalate(214341-15-8)

  • 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: 214341-15-8(Hazardous Substances Data)

214341-15-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 214341-15-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,4,3,4 and 1 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 214341-15:
(8*2)+(7*1)+(6*4)+(5*3)+(4*4)+(3*1)+(2*1)+(1*5)=88
88 % 10 = 8
So 214341-15-8 is a valid CAS Registry Number.

214341-15-8Relevant articles and documents

Discovery of MC-02,331, a new cephalosporin exhibiting potent activity against methicillin-resistant staphylococcus aureus

Hecker, Scott J.,Cho, In-Seop,Glinka, Tomasz W.,Zhang, Zhijia J.,Price, Mary E.,Lee, Ving J.,Christensen, Burton G.,Boggs, Amy,Chamberland, Suzanne,Malouin, Francois,Parr, Thomas R.,Annamalai, Thamil,Blais, Johanne,Bond, Emmett L.,Case, Laura,Chan, Christine,Crase, Jac,Frith, Ria,Griffith, David,Harford, Laurie,Liu, Nancy,Ludwikow, Maria,Mathias, Kristina,Rea, David,Williams, Robert

, p. 722 - 734 (2007/10/03)

A systematic approach toward building activity against methicillin-resistant staphylococci into the cephalosporin class of β-lactam antibiotics is described. Initial work focused on finding the optimal linkage between the cephem nucleus and a biphenyl pha

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