Methoxycarbonyl-L-tert-leucine CAS NO.162537-11-3 CAS NO.162537-11-3
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- Product Details
Keywords
- Methoxycarbonyl-L-tert-leucine
- MOC-L-tert.Leucine
- (S)-2-Methoxycarbonylamino-3,3-dimethylbutyric acid
Quick Details
- ProName: Methoxycarbonyl-L-tert-leucine CAS NO....
- CasNo: 162537-11-3
- Molecular Formula: C8H15NO4
- Appearance: colourless viscous liquid
- Application: Synthetic fragrances
- DeliveryTime: In stock
- PackAge: drum
- Port: China main port
- ProductionCapacity: 10000 Metric Ton/Month
- Purity: 99%
- Storage: Room temperature
- Transportation: By Sea/Air/DHL
- LimitNum: 1 Kilogram
- first class: 1-10
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Details
Methoxycarbonyl-L-tert-leucine Basic information |
Product Name: | Methoxycarbonyl-L-tert-leucine |
Synonyms: | MOC-L-tert.Leucine;(S)-2-Methoxycarbonylamino-3,3-dimethylbutyric acid;Methoxycarbonyl-L-tert-leucine;N-(Methoxycarbonyl)-3-methyl-L-valine;N-Methoxycarbonyl-tert-leucine;Atazanavir related coMpound A;MOC-L-tert. Leucin;L-Valine,N-(Methoxycarbonyl)-3-Methyl- |
CAS: | 162537-11-3 |
MF: | C8H15NO4 |
MW: | 189.21 |
EINECS: | 1308068-626-2 |
Product Categories: | Amino Acid Derivatives;Amino Acids 13C, 2H, 15N;Amino Acids & Derivatives;Chiral Reagents |
Mol File: | 162537-11-3.mol |
Methoxycarbonyl-L-tert-leucine Chemical Properties |
Melting point | 1090C |
Boiling point | 320.9±25.0 °C(Predicted) |
density | 1.126±0.06 g/cm3(Predicted) |
storage temp. | 2-8°C |
solubility | Soluble in ethyl acetate and methanol. |
pka | 4.46±0.10(Predicted) |
form | powder |
InChIKey | NWPRXAIYBULIEI-RXMQYKEDSA-N |
Safety Information |
HS Code | 2933399090 |
MSDS Information |
Methoxycarbonyl-L-tert-leucine Usage And Synthesis |
Description | Methoxycarbonyl-L-tert-leucine is a kind of amino acid deriviative. It is a very useful intermediate for efficient synthesis of the HIV protease inhibitor BMS-232632 as well as atazanavir bisulfate. |
References | Zhongmin Xu, †, et al. "Process Research and Development for an Efficient Synthesis of the HIV Protease Inhibitor BMS-232632." Organic Process Research & Development 6.3(2002):323-328. Simhadri, Srinivas. "Process for the preparation of atazanavir bisulfate." (2016). # q=14328-63-3 |
Chemical Properties | White Solid |
Uses | The coupling of the two key intermediates, N-(methoxycarbonyl)-l-tert-leucine acylated benzyl hydrazine and chloromethyl ketone, via an S N 2 reaction furnished the amino ketone in high yield under our optimized conditions in practical synthesis of the HIV Protease Inhibitor Atazanavir via a Highly diastereoselective Reduction Approach. |