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CAS RN: 130525-58-5 | Product Number: A3442
Zanamivir Azide Triacetate Methyl Ester
Purity: >95.0%(HPLC)
Synonyms:
- (1S,2R)-1-[(2R,3R,4S)-3-Acetamido-4-azido-6-(methoxycarbonyl)-3,4-dihydro-2H-pyran-2-yl]propane-1,2,3-triyl Triacetate
- D-Glycero-D-galacto-non-2-enonic Acid
Product Documents:
Size | Unit Price | Same Day | 2-3 Business Days | Other Lead Time | Shipping Information |
---|---|---|---|---|---|
50MG |
₩253,500
|
19 | 0 | Contact Us |
* Please contact our distributor of SEJIN CI Co., Ltd.
if you would like to purchase TCI products. The above prices do not include freight cost, customs charge and other charges to the destination. SEJIN CI Co., Ltd. (Phone: 02-2655-2480 / email:
sales@sejinci.co.kr)
* The storage conditions are subject to change without notice.
* The storage conditions are subject to change without notice.
Product Number | A3442 |
Purity / Analysis Method | >95.0%(HPLC) |
Molecular Formula / Molecular Weight | C__1__8H__2__4N__4O__1__0 = 456.41 |
Physical State (20 deg.C) | Solid |
Storage Temperature | Refrigerated (0-10°C) |
Store Under Inert Gas | Store under inert gas |
Condition to Avoid | Air Sensitive,Heat Sensitive |
Packaging and Container | 50MG-Glass Bottle with Plastic Insert (View image) |
CAS RN | 130525-58-5 |
Reaxys Registry Number | 4359783 |
PubChem Substance ID | 468590302 |
MDL Number | MFCD08704809 |
Specifications
Appearance | White to Light yellow powder to crystal |
Purity(HPLC) | min. 95.0 area% |
Melting point | 90.0 to 94.0 °C |
Specific rotation | +102 to +108 deg(C=1, CHCl3) |
NMR | confirm to structure |
Properties (reference)
Melting Point | 91 °C |
GHS
Related Laws:
Transport Information:
H.S.code* | 2932.99-000 |
Application
A Key Synthetic Intermediate of Zanamivir and its Analogs
This product has been used as a key synthetic intermediate of zanamivir [Z0023] which is an influenza virus neuraminidase inhibitor, and its analogs.
References
- The synthesis of 2,3-didehydro-2,4-dideoxy-4-guanidinyl-N-acetylneuraminic acid: a potent influenza virus sialidase inhibitor
- Synthesis of the potent influenza neuraminidase inhibitor 4-guanidino Neu5Ac2en. X-ray molecular structure of 5-acetamido-4-amino-2,6-anhydro-3,4,5-trideoxy-D-erythro-L-gluco-nonionic acid
- Syntheses of triazole-modified zanamivir analogs via click chemistry and anti-AIV activities
Product Documents (Note: Some products will not have analytical charts available.)
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Specifications
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