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CAS RN: 104146-10-3 | Product Number: M2411
4-Methoxybenzyl 3-Chloromethyl-7-(2-phenylacetamido)-3-cephem-4-carboxylate
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Purity: >98.0%(N)
Synonyms:
- 3-Chloromethyl-7-(2-phenylacetamido)-3-cephem-4-carboxylic Acid 4-Methoxybenzyl Ester
Product Documents:
| Size | Unit Price | Shanghai | Tianjin | Japan* |
|---|---|---|---|---|
| 5G |
¥190.00
|
2 | 1 | 8 |
| 25G |
¥280.00
|
3 | 1 | 27 |
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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:
| Customs Control Conditions (Q) |
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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Specifications
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