BOC-L-Proline CAS 15761-39-4
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Chemical Name: BOC-L-Proline CAS 15761-39-4
CAS No.: 15761-39-4
Molecular Fomula: C10H17NO4
Molecular weight: 215.25
Appearance: White Crystals or Crystalline Powder
Sample: Available
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Description of BOC-L-Proline
N-Boc-L-proline is a useful synthetic intermediate. It is used to synthesize Daclatasvir which nhibits the HCV protein NS5A. Daclatasvir can be used as a drug candidate for the treatment of hepatitis C (HCV).
Basic Info of BOC-L-Proline
Chemical Name | BOC-L-Proline |
Synonyms | Boc-L-Proline;N-(tert-Butyloxycarbonyl)-L-proline;N-(tert-Butoxycarbonyl)-L-proline;(S)-1-(tert-Butoxycarbonyl)pyrrolidine-2-carboxylic acid;N-Boc-L-proline; |
CAS No. | 15761-39-4 |
Molecular Formula | C10H17NO4 |
Molecular Weight | 215.24600 |
PSA | 66.84000 |
LogP | 1.40840 |
Safety Info
HS Code | 2933990090 |
Properties
Appearance & Physical State | White to off-white crystalline powder |
Density | 1.201 g/cm3 |
Boiling Point | 337.2ºC at 760 mmHg |
Melting Point | 133-136ºC |
Flash Point | 157.7ºC |
Stability | Stable at room temperature in closed containers under normal storage and handling conditions. |
Storage Condition | Store at RT. |
Vapor Pressure | 2E-05mmHg at 25°C |
Numbering system
MDL number | MFCD00037324 |
EINECS number | 239-848-3 |
PubChem number | 24849310 |
BRN number | 15828 |
What is BOC-L-Proline?
With the progress of science and technology and the development of society, chemical products have invariably permeated our daily lives, in medicine, food, cosmetics, electronics, industry, and other areas, becoming an essential part of our lives. One such product is BOC-L-Proline which has developed particularly rapidly in recent years. Do you know about BOC-L-Proline?
The official answer: BOC-L-proline is a chemical compound with the molecular formula C10H17NO4.
What’s the application of BOC-L-Proline?
BOC-L-proline is a useful synthetic intermediate. It is used in the synthesis of Daclatasvir (D101500) which inhibits the HCV protein NS5A. Daclatasvir (D101500) can be used as a drug candidate for the treatment of hepatitis C (HCV).
Conclusion
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