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Cefetamet pivoxil hydrochloride
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Cefetamet pivoxil hydrochloride

CAS: 111696-23-2

Ref. 3D-FC40876

5gDiscontinued
10gDiscontinued
25gDiscontinued
50gDiscontinued
100gDiscontinued

Discontinued product. For inquiries about similar products, please fill out our form or email us at .


Product Information

Name:
Cefetamet pivoxil hydrochloride
Synonyms:
  • 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[(2-amino-4-thiazolyl)(methoxyimino)acetyl]amino]-3-methyl-8-oxo-, (2,2-dimethyl-1-oxopropoxy)methyl ester, monohydrochloride, [6R-[6α,7β(Z)]]-
  • 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[(2Z)-(2-amino-4-thiazolyl)(methoxyimino)acetyl]amino]-3-methyl-8-oxo-, (2,2-dimethyl-1-oxopropoxy)methyl ester, monohydrochloride, (6R,7R)-
  • 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[(2Z)-2-(2-amino-4-thiazolyl)-2-(methoxyimino)acetyl]amino]-3-methyl-8-oxo-, (2,2-dimethyl-1-oxopropoxy)methyl ester, hydrochloride (1:1), (6R,7R)-
  • Cefetamet (pivaloyloxy)methyl ester hydrochloride
  • Cefetamet Pivoxil Hydrochloride
  • Cefyl
  • Ro 15-8075
  • [(2,2-dimethylpropanoyl)oxy]methyl (6R,7R)-7-{[(2E)-2-(2-amino-1,3-thiazol-4-yl)-2-(methoxyimino)acetyl]amino}-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate hydrochloride
  • [(2,2-dimethylpropanoyl)oxy]methyl (6R,7R)-7-{[(2Z)-2-(2-amino-1,3-thiazol-4-yl)-2-(methoxyimino)acetyl]amino}-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate hydrochloride
Description:

Cefetamet pivoxil hydrochloride is an antimicrobial agent that belongs to the class of cephalosporin antibiotics and is used as a second-line drug in the treatment of respiratory tract infections. It is active against Gram-positive bacteria, such as Streptococcus pneumoniae and Staphylococcus aureus, but not against Gram-negative bacteria such as Escherichia coli. Cefetamet pivoxil hydrochloride inhibits bacterial growth by binding to penicillin-binding proteins, which are located in the cell wall of bacteria. The reaction mechanism for this antibiotic follows the same pathway as other cephalosporins: it binds to penicillin-binding proteins, which are located in the cell wall of bacteria. The reaction mechanism for this antibiotic follows the same pathway as other cephalosporins: it binds to penicillin-binding proteins, which are located in the cell wall of bacteria.

Notice:
Our products are intended for lab use only. For any other use, please contact us.
Brand:
Biosynth
Long term storage:
Notes:

Chemical properties

Molecular weight:
548.03 g/mol
Formula:
C20H25N5O7S2·HCl
Purity:
Min. 95%
MDL:
Melting point:
Boiling point:
Flash point:
Density:
Concentration:
EINECS:
Merck:
HS code:

Hazard Info

UN Number:
EQ:
Class:
H Statements:
P Statements:
Forbidden to fly:
Hazard Info:
Packing Group:
LQ:

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