Introduction：Basic information about CAS 24277-39-2|Boc-Glu-OtBu, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
| Common Name | Boc-Glu-OtBu |
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| CAS Number | 24277-39-2 | Molecular Weight | 303.351 |
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| Density | 1.1±0.1 g/cm3 | Boiling Point | 449.8±40.0 °C at 760 mmHg |
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| Molecular Formula | C14H25NO6 | Melting Point | 113 °C |
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| MSDS | ChineseUSA | Flash Point | 225.8±27.3 °C |
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Names
| Name | (4S)-5-[(2-methylpropan-2-yl)oxy]-4-[(2-methylpropan-2-yl)oxycarbonylamino]-5-oxopentanoic acid |
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| Synonym | More Synonyms |
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Boc-Glu-OtBu BiologicalActivity
| Description | Boc-Glu-OtBu is a glutamic acid 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 | 1.1±0.1 g/cm3 |
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| Boiling Point | 449.8±40.0 °C at 760 mmHg |
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| Melting Point | 113 °C |
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| Molecular Formula | C14H25NO6 |
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| Molecular Weight | 303.351 |
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| Flash Point | 225.8±27.3 °C |
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| Exact Mass | 303.168182 |
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| PSA | 101.93000 |
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| LogP | 2.82 |
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| Vapour Pressure | 0.0±2.3 mmHg at 25°C |
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| Index of Refraction | 1.470 |
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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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| RIDADR | NONH for all modes of transport |
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| WGK Germany | 3 |
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Articles1
More Articles
| Folding graft copolymer with pendant drug segments for co-delivery of anticancer drugs. Biomaterials 35(25) , 7194-203, (2014) A graft copolymer with pendant drug segments can fold into nanostructures in a protein folding-like manner. The graft copolymer is constructed by directly polymerizing γ-camptothecin-glutamate N-carbo... | |
Synonyms
| Boc-L-glutamicacid1-tert-butylester |
| Boc-L-glutamic acid 1-tert-butyl ester |
| MFCD00038273 |
| N-(tert-Butoxycarbonyl)-L-glutamic Acid 1-tert-Butyl Ester |
| N-Boc-Glu-OtBu |
| N-(t-butoxycarbonyl)-L-glutamic acid t-butyl ester |
| Boc-Glu-Otbu |
| N-Boc-L-glutamic acid 1-tert-butyl ester |
| 1-tert-Butyl N-(tert-Butoxycarbonyl)-L-glutamate |
| (S)-5-tert-butoxy-4-tert-butoxycarbonylamino-5-oxo-pentanoic acid |
| (4S)-5-[(2-Methyl-2-propanyl)oxy]-4-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)-5-oxopentanoic acid |
| 5-[(2-Methyl-2-propanyl)oxy]-4-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)-5-oxopentanoic acid |
| (4S)-5-tert-Butoxy-4-[(tert-butoxycarbonyl)amino]-5-oxopentanoic acid (non-preferred name) |
| Glutamic acid, N-[(1,1-dimethylethoxy)carbonyl]-, 1-(1,1-dimethylethyl) ester |
| 1-tert-Butyl N-Boc-L-glutamate |
| L-Glutamic acid, N-[(1,1-dimethylethoxy)carbonyl]-, 1-(1,1-dimethylethyl) ester |
