Ceftezole

Base Information

Chemical Name:Ceftezole
CAS No.:26973-24-0
Molecular Formula:C₁₃H₁₂N₈O₄S₃
Molecular Weight:440.487
Hs Code.:3003201400
UNII:2Z86SYP11W
DSSTox Substance ID:DTXSID0022771
Nikkaji Number:J9.795K
Wikipedia:Ceftezole
Wikidata:Q5057295
NCI Thesaurus Code:C76038
Metabolomics Workbench ID:154599
ChEMBL ID:CHEMBL1697829
Mol file:26973-24-0.mol

Synonyms:ceftezol;ceftezol, sodium salt;ceftezole;ceftezole sodium;Celoslin;demethylcefazolin;Falomesin

Suppliers and Price of Ceftezole

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
Ceftezole
10g
$ 85.00

Sigma-Aldrich
Cadmium zinc telluride 99.9999% trace metals basis
5g
$ 124.00

Chem-Impex
Ceftezole,98%(HPLC) 98%(HPLC)
25G
$ 262.08

Chem-Impex
Ceftezole,98%(HPLC) 98%(HPLC)
5G
$ 72.80

Biosynth Carbosynth
Ceftezole
50 g
$ 400.00

Biosynth Carbosynth
Ceftezole
10 g
$ 144.00

Biosynth Carbosynth
Ceftezole
2 g
$ 50.00

Biosynth Carbosynth
Ceftezole
5 g
$ 90.00

Biosynth Carbosynth
Ceftezole
25 g
$ 250.00

AK Scientific
Ceftezole
25g
$ 236.00

Total 80 raw suppliers

Chemical Property of Ceftezole

Chemical Property:

Melting Point:155 °C (dec.)
Refractive Index:2.003
PKA:2.60±0.50(Predicted)
PSA：234.93000
Density:2.09 g/cm³
LogP:-0.61570
XLogP3:-0.7
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:12
Rotatable Bond Count:7
Exact Mass:440.01436441
Heavy Atom Count:28
Complexity:709

Purity/Quality:

99% ^*data from raw suppliers

Ceftezole ^*data from reagent suppliers

Safty Information:

Pictogram(s): T+,N
Hazard Codes:T+,N
Statements: 21/22-26-50/53
Safety Statements: 28-36/37-45-61

MSDS Files:

Useful:

Canonical SMILES:C1C(=C(N2C(S1)C(C2=O)NC(=O)CN3C=NN=N3)C(=O)O)CSC4=NN=CS4
Isomeric SMILES:C1C(=C(N2[C@H](S1)[C@@H](C2=O)NC(=O)CN3C=NN=N3)C(=O)O)CSC4=NN=CS4
Uses Ceftezole is a β-lactam, cephem antibiotic. It also exhibits potent α-glucosidase inhibitory activity and antidiabetic effect in streptozotocin-induced mouse. A direct bandgap semiconductor, it is used in a variety of applications, including radiation detectors, photorefractive gratings, electro-optic modulators, solar cells, and terahertz generation and detection. The band gap varies from approximately 1.4 to 2.2 eV, depending on composition.
Therapeutic Function Antibiotic

Technology Process of Ceftezole

There total 3 articles about Ceftezole which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 91.0%

: 21744-54-7
tert-butyl 2-(1H-1,2,3,4-tetrazol-1-yl)acetate

: 7-amino-3-chloromethyl-3-cephem-4-carboxylic acid

: 18686-82-3
2-mercapto-1,3,4-thiadiazole

: 26973-24-0
ceftezole

Guidance literature:: 7-amino-3-chloromethyl-3-cephem-4-carboxylic acid; 2-mercapto-1,3,4-thiadiazole; With alumina; N-benzyl-N-decyl-N,N-dimethylammonium chloride; magnesium acetate; potassium hydroxide; calcium hydroxide; In cyclohexanone; at 10 ℃; for 10h;

tert-butyl 2-(1H-1,2,3,4-tetrazol-1-yl)acetate; In cyclohexanone; at 20 ℃; for 1h; Reagent/catalyst; Temperature;