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p-nitrobenzyl 7β-(2-thienylacetamido)-3-(acetoxymethyl)-3-cephem-4-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 41625-53-0 Structure
  • Basic information

    1. Product Name: p-nitrobenzyl 7β-(2-thienylacetamido)-3-(acetoxymethyl)-3-cephem-4-carboxylate
    2. Synonyms: p-nitrobenzyl 7β-(2-thienylacetamido)-3-(acetoxymethyl)-3-cephem-4-carboxylate
    3. CAS NO:41625-53-0
    4. Molecular Formula:
    5. Molecular Weight: 531.567
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 41625-53-0.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: p-nitrobenzyl 7β-(2-thienylacetamido)-3-(acetoxymethyl)-3-cephem-4-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: p-nitrobenzyl 7β-(2-thienylacetamido)-3-(acetoxymethyl)-3-cephem-4-carboxylate(41625-53-0)
    11. EPA Substance Registry System: p-nitrobenzyl 7β-(2-thienylacetamido)-3-(acetoxymethyl)-3-cephem-4-carboxylate(41625-53-0)
  • 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: 41625-53-0(Hazardous Substances Data)

41625-53-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41625-53-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,6,2 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 41625-53:
(7*4)+(6*1)+(5*6)+(4*2)+(3*5)+(2*5)+(1*3)=100
100 % 10 = 0
So 41625-53-0 is a valid CAS Registry Number.

41625-53-0Relevant articles and documents

Process for preparing cephalosporin esters in the presence of liquid sulfur dioxide

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, (2008/06/13)

A process for preparing a cephalosporin ester which comprises subjecting an organic halide or an alcohol to reaction with a cephalosporin acid, a cephalosporin acid halide or a salt thereof in the presence of liquid sulfur dioxide.

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