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CAS RN: 104146-10-3 | Product Number: M2411
4-Methoxybenzyl 3-Chloromethyl-7-(2-phenylacetamido)-3-cephem-4-carboxylate
Purity: >98.0%(N)
Synonyms:
- 3-Chloromethyl-7-(2-phenylacetamido)-3-cephem-4-carboxylic Acid 4-Methoxybenzyl Ester
Product Documents:
Size | Unit Price | Same Day | 2-3 Business Days |
---|---|---|---|
5G |
$21.00
|
3 | 8 |
25G |
$69.00
|
30 | 2 |
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Product Number | M2411 |
Purity / Analysis Method | >98.0%(N) |
Molecular Formula / Molecular Weight | C__2__4H__2__3ClN__2O__5S = 486.97 |
Physical State (20 deg.C) | Solid |
Storage Temperature | Frozen (<0°C) |
Condition to Avoid | Heat Sensitive |
CAS RN | 104146-10-3 |
Reaxys Registry Number | 4894110 |
PubChem Substance ID | 253659829 |
MDL Number | MFCD00191253 |
Specifications
Appearance | White to Orange to Green powder to crystal |
Purity(with Total Nitrogen) | min. 98.0 % |
Properties (reference)
Melting Point | 153 °C(dec.) |
GHS
Related Laws:
RTECS# | XI0369883 |
Transport Information:
H.S.code* | 2941.90-000 |
Application
Synthesis of Cehem 3-Side Chains and Cefditoren Pivoxil (ME1207)
This product is used to synthesize a compound with a modification of the 3-side chain of cephem antibiotics, such as cefditoren pivoxil (ME1207) [C2856].
References
- Palladium catalysis in cephalosporin chemistry: general methodology for the synthesis of cephem side chains
- Synthesis of cephalosporin-3′-diazeniumdiolates: biofilm dispersing NO-donor prodrugs activated by β-lactamase
- The Stille Reaction
- A Facile Access to 3-Cephems by Employing Novel Lewis Acid Mediated Reaction
- Synthesis and oral activity of pivaloyloxymethyl 7-[(Z)-2-(2-aminothiazol-4-yl)-2-methoxyiminoacetamido]-3(Z)-(4- methylthiazol-5-yl)vinyl-3-cephem-4-carboxylate (ME1207) and its related compound
- Synthesis and oral activity of ME 1207, a new orally active cephalosporin
PubMed Literature
Product Documents (Note: Some products will not have analytical charts available.)
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