Boc-L-homoserine structure
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Common Name | Boc-L-homoserine | ||
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CAS Number | 41088-86-2 | Molecular Weight | 219.235 | |
Density | 1.2±0.1 g/cm3 | Boiling Point | 421.6±40.0 °C at 760 mmHg | |
Molecular Formula | C9H17NO5 | Melting Point | 140°C(lit.) | |
MSDS | Chinese USA | Flash Point | 208.8±27.3 °C |
Use of Boc-L-homoserineBoc-L-Homoserine is a serine derivative[1]. |
Name | Boc-L-homoserine |
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Synonym | More Synonyms |
Description | Boc-L-Homoserine is a serine derivative[1]. |
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Related Catalog | |
In Vitro | Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1]. |
References |
Density | 1.2±0.1 g/cm3 |
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Boiling Point | 421.6±40.0 °C at 760 mmHg |
Melting Point | 140°C(lit.) |
Molecular Formula | C9H17NO5 |
Molecular Weight | 219.235 |
Flash Point | 208.8±27.3 °C |
Exact Mass | 219.110672 |
PSA | 95.86000 |
LogP | 0.69 |
Vapour Pressure | 0.0±2.3 mmHg at 25°C |
Index of Refraction | 1.485 |
Storage condition | −20°C |
Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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Hazard Codes | Xi |
Safety Phrases | 26-36-37/39 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
HS Code | 2924199090 |
Precursor 7 | |
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DownStream 3 | |
HS Code | 2924199090 |
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Summary | 2924199090. other acyclic amides (including acyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0% |
Synthesis of the functionalizable methionine surrogate azidohomoalanine using Boc-homoserine as precursor.
Nat. Protoc. 2 , 1884-1887, (2007) This protocol describes a synthetic route to the non-canonical amino acid azidohomoalanine (AHA) using protected homoserine as a starting material. An alternative route to AHA is presented in a compan... |
L-Homoserine, N-[(1,1-dimethylethoxy)carbonyl]- |
N-Boc-L-Homoserine |
Boc-L-Homoserine |
(2S)-4-hydroxy-2-[(2-methylpropan-2-yl)oxycarbonylamino]butanoic acid |
N-(tert-Butoxycarbonyl)-L-homoserine |
(S)-2-((tert-Butoxycarbonyl)amino)-4-hydroxybutanoic acid |
(S)-2-(Boc-amino)-4-hydroxybutyric Acid |
Boc-Homoser-OH |
N-T-Boc-L-Homoserine |
Boc-Homoserine |
N-{[(2-Methyl-2-propanyl)oxy]carbonyl}-L-homoserine |
(S)-2-(tert-Butoxycarbonylamino)-4-hydroxybutyric Acid |