Introduction：Basic information about CAS 41088-86-2|Boc-L-homoserine, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
| Common Name | Boc-L-homoserine |
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| CAS Number | 41088-86-2 | Molecular Weight | 219.235 |
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| Density | 1.2±0.1 g/cm3 | Boiling Point | 421.6±40.0 °C at 760 mmHg |
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| Molecular Formula | C9H17NO5 | Melting Point | 140°C(lit.) |
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| MSDS | ChineseUSA | Flash Point | 208.8±27.3 °C |
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Names
| Name | Boc-L-homoserine |
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| Synonym | More Synonyms |
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Boc-L-homoserine BiologicalActivity
| Description | Boc-L-Homoserine is a serine derivative[1]. |
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| Related Catalog | Research Areas >>OthersSignaling Pathways >>Others >>Others |
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| 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]. |
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| References | [1]. Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1144. |
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Chemical & Physical Properties
| Density | 1.2±0.1 g/cm3 |
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| Boiling Point | 421.6±40.0 °C at 760 mmHg |
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| Melting Point | 140°C(lit.) |
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| Molecular Formula | C9H17NO5 |
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| Molecular Weight | 219.235 |
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| Flash Point | 208.8±27.3 °C |
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| Exact Mass | 219.110672 |
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| PSA | 95.86000 |
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| LogP | 0.69 |
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| Vapour Pressure | 0.0±2.3 mmHg at 25°C |
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| Index of Refraction | 1.485 |
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| InChIKey | PZEMWPDUXBZKJN-LURJTMIESA-N |
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| SMILES | CC(C)(C)OC(=O)NC(CCO)C(=O)O |
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| Storage condition | −20°C |
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Safety Information
| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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| Hazard Codes | Xi |
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| Safety Phrases | 26-36-37/39 |
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| RIDADR | NONH for all modes of transport |
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| WGK Germany | 3 |
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| HS Code | 2924199090 |
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Customs
| 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% |
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Articles1
More Articles
| 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... | |
Synonyms
| 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 |
