Boc-L-Proline structure
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Common Name | Boc-L-Proline | ||
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CAS Number | 15761-39-4 | Molecular Weight | 215.25 | |
Density | 1.2±0.1 g/cm3 | Boiling Point | 337.2±35.0 °C at 760 mmHg | |
Molecular Formula | C10H17NO4 | Melting Point | 133-136ºC | |
MSDS | USA | Flash Point | 157.7±25.9 °C |
Use of Boc-L-ProlineBoc-L-proline is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
Name | BOC-L-Proline |
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Synonym | More Synonyms |
Description | Boc-L-proline is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
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Related Catalog |
Density | 1.2±0.1 g/cm3 |
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Boiling Point | 337.2±35.0 °C at 760 mmHg |
Melting Point | 133-136ºC |
Molecular Formula | C10H17NO4 |
Molecular Weight | 215.25 |
Flash Point | 157.7±25.9 °C |
Exact Mass | 215.115753 |
PSA | 66.84000 |
LogP | 0.56 |
Vapour Pressure | 0.0±1.6 mmHg at 25°C |
Index of Refraction | 1.503 |
Storage condition | 2~8°C |
Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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Hazard Codes | Xn |
Risk Phrases | 20/21/22-36/37/38 |
Safety Phrases | S24/25 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
HS Code | 2933990090 |
Precursor 10 | |
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DownStream 10 | |
HS Code | 2933990090 |
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Summary | 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
Transport and signaling via the amino acid binding site of the yeast Gap1 amino acid transceptor.
Nat. Chem. Biol. 5 , 45-52, (2009) Transporter-related nutrient sensors, called transceptors, mediate nutrient activation of signaling pathways through the plasma membrane. The mechanism of action of transporting and nontransporting tr... |
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Complexation-Driven Mutarotation in Poly(L-proline) Block Copolypeptides.
Biomacromolecules 16 , 3686-93, (2015) Novel poly(L-lysine)-block-poly(L-proline) (PLL-b-PLP)-based materials with all PLP helical conformers, i.e., PLP II and the rare PLP I are here reported. Electrostatic supramolecular complexation of ... |
1-(tert-butoxycarbonyl)-L-proline |
Boc-L-Pro-OH |
tert-Butyloxycarbonyl-L-proline |
1,2-Pyrrolidinedicarboxylic acid, 1-(1,1-dimethylethyl) ester, (2S)- |
N-(tert-Butyloxycarbonyl)-L-proline |
MFCD00037324 |
1-{[(2-Methyl-2-propanyl)oxy]carbonyl}-L-proline |
Boc-L-Proline |
1,2-Pyrrolidinedicarboxylic acid, 1- (1,1-dimethylethyl) ester, (S)- |
EINECS 239-848-3 |
N-(tert-Butoxycarbonyl)-L-proline |
(S)-1-(tert-Butoxycarbonyl)pyrrolidine-2-carboxylic acid |
(2S)-1-{[(2-Methyl-2-propanyl)oxy]carbonyl}-2-pyrrolidinecarboxylic acid |
N-Boc-L-proline |
1-tert-Butyloxycarbonyl-L-proline |
Boc-Pro-OH |