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Cefoxitin CAS 35607-66-0 Effective Treatment

Product Details

Place of Origin: China

Brand Name: Sunshine

Certification: ISO,COA

Model Number: 35607-66-0

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Minimum Order Quantity: Negotiation

Price: Negotiation

Packaging Details: Bag,Drum

Delivery Time: 7-15 days

Payment Terms: L/C, D/A, T/T, Western Union

Supply Ability: TON

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CAS 35607-66-0 Cefoxitin

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CAS 35607-66-0

CAS NO::
35607-66-0
Appearance::
White To Off-white Crystalline Powder
Molecular Formula::
C16H17N3O7S2
Molecular Weight::
427.45200
EINECS NO::
252-641-2
MDL NO::
MFCD00072014
CAS NO::
35607-66-0
Appearance::
White To Off-white Crystalline Powder
Molecular Formula::
C16H17N3O7S2
Molecular Weight::
427.45200
EINECS NO::
252-641-2
MDL NO::
MFCD00072014
Cefoxitin CAS 35607-66-0 Effective Treatment

Product Description:

Product Name: Cefoxitin CAS NO: 35607-66-0

 

 

Synonyms:

(6r-cis)-ethyl)-7-metho-xy-8-oxo-7-((2-thienylacetyl)amino);

Cefoxitin{(6R-cis)-3-[(Carbamoyloxy)methyl]-7-metho-xy-8-oxo-7-(2-thienylacetamido)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid};

 

 

Chemical & Physical Properties:

Appearance: White to off-white crystalline powder

Assay :≥99.0%

Density: 1.63 g/cm3

Boiling Point: 843.4℃ at 760 mmHg

Melting Point: 149 – 150℃

Refractive Index: 1.692

Water Solubility: Predicted solubility in water is less than 0.2mg/ml

 

 

Safety Information:

HS Code: 3003201300

Packing Group: III

RIDADR: UN 3077

 

 

Cefoxitin is a semi-synthetic antibiotic derived from Cephamycin C, possessing high resistance to β-lactamase inactivation. An antibacterial. Cefoxitin contains the same C-7 side chain as cephalothin and the same C-3 side chain as cefuroxime. The most novel chemical feature of cefoxitin is the possession of an α-oriented metho-xyl group in place of the normal H-atom at C-7. This increased steric bulk conveys very significant stability against β-lactamases. The inspiration for these functional groups was provided by the discovery of the naturally occurring antibiotic cephamycin C derived from fermentation of Streptomyces lactamdurans. Cephamycin C itself has not seen clinical use but, rather, has provided the structural clue that led to useful agents such as cefoxitin. Agents that contain this 7α metho-xy group are commonly referred to as cephamycins. Ingenious chemical transformations now enable synthetic introduction of such a metho-xy group into cephalosporins lacking this feature.

 

 

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