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Cefaclor Dimer

SZ CAT No SZ-C067023
CAS No NA
Mol.F. C30H26Cl2N6O7S2
Mol.Wt. 717.6
Inv. Status Custom Synthesis


Chemical Name: (6R,7R)-7-((R)-2-((6R,7R)-7-((R)-2-Amino-2-phenylacetamido)-3-chloro-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxamido)-2-phenyl acetamido)-3-chloro-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

Smiles: O=C(C(N12)=C(Cl)CS[C@]2([H])[C@H](NC([C@H](NC(C(N34)=C(Cl)CS[C@]4([H])[C@H](NC([C@H](N)C5=CC=CC=C5)=O)C3=O)=O)C6=CC=CC=C6)=O)C1=O)O

Inchi: InChI=1S/C21H24F3N3S/c1-25-11-13-26(14-12-25)9-4-10-27-17-5-2-3-6-19(17)28-20-8-7-16(15-18(20)27)21(22,23)24/h2-3,5-8,15H,4,9-14H2,1H3

Multidimensional evaluation of impurity profiles for generic cephalexin and cefaclor antibiotics
B.A. Olsen*, S.W. Baertschi and R.M. Riggin
Journal of Chromatography, 648 (1993) 165-173
 
Mass Spectral Profile for Rapid Differentiating Beta-Lactams from Their Ring-Opened Impurities
Hecheng Wang,1,2 Haiwei Huang,3 Jin Cao,3 Dehua Chui,2 and Shengyuan Xiao
Hindawi Publishing Corporation BioMed Research International Volume 2015, Article ID 697958, 13 pages
 
The Degradation Mechanism of an Oral Cephalosporin: Cefaclor
Bartolomê Vilanova  Josefa Donoso  Francisco Muñoz  Francisco García‐Blanco
helvetica chimica acta - vol. 79 (1996)