| Name | tert-butyl 2-[(2-methylpropan-2-yl)oxycarbonylamino]acetate |
|---|---|
| Synonyms |
N-(TERT-BUTOXYCBONYL)GLYCINE TERT-BUTYL ESTER
BOC-GLY-OTBU N-Boc-gL BOC-GLYCINE T-BUTYL ESTER N-(tert-Butoxycbonyl)glycine tert-Butyl Ester > ert-butyl2-[(2-methylpropan-2-yl)oxycbonylamino]acetate tert-Butyl 2-((tert-butoxycbonyl)amino)acetate N-Boc-glycine t-butyl ester MFCD00191866 N-alpha-t-Butyloxycbonyl-glycine t-butyl ester 2-Methyl-2-propanyl N-{[(2-methyl-2-propanyl)oxy]carbonyl}glycinate Boc-Gly-Ot< tert-butyl 2-(tert-butoxycbonyl)acetate N-(tert-Butoxycbonyl)glycine tert-butyl ester (tert-Butoxycbonylamino)acetic acid tert-butyl ester BOC-GLYCINE TERT-BUTYL ESTER t-BuO2CCH2NHBoc Boc-glycine tert-butyl ester tert-butyl 2-[(2-methylpropan-2-yl)oxycbonylamino]acetate (Tert-Butoxy)carbonyl Gly-OtBu tert-butyl N-Boc-glycinate N-Boc-glycine tert-butyl ester (tert-Butoxycbonylamino)acetic acid tert-butyl ester Glycine, N-[(1,1-dimethylethoxy)carbonyl]-, 1,1-dimethylethyl ester N-BOC-Gly-OtBu tert-butyl N-(tert-butoxycbonyl)glycinate Boc-Glycine N-(tert-Butoxycarbonyl)-3-methyl-L-valine Boc-Gly-Otbu-OH Tert butyloxycbonylglycine tert butyl ester N-Boc-glycine tert-Butyl Ester BOC-GLYCINE TERT-BUTYL ESTER //BP BOC-GLYCINETERT-BUTYLESTER 3-Methyl-N-{[(2-methyl-2-propanyl)oxy]carbonyl}-L-valine Boc-Gly-OtBu Glycine, N-[(1,1-diMethylethoxy)carbonyl]-, 1,1-diMethylethyl ester N-(tert-Butoxycbonyl)glycine tert-Butyl Este Boc-glycinetert-butyl ester (HPLC) tert-Butyl 2-((tert-butoxycarbonyl)amino)acetate |
| Description | tert-Butyl 2-((tert-butoxycarbonyl)amino)acetate is a Glycine (HY-Y0966) derivative[1]. |
|---|---|
| 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 | 1.0±0.1 g/cm3 |
|---|---|
| Boiling Point | 306.0±25.0 °C at 760 mmHg |
| Melting Point | 66-68ºC(lit.) |
| Molecular Formula | C11H21NO4 |
| Molecular Weight | 231.289 |
| Flash Point | 138.9±23.2 °C |
| Exact Mass | 231.147064 |
| PSA | 64.63000 |
| LogP | 2.44 |
| Vapour Pressure | 0.0±0.6 mmHg at 25°C |
| Index of Refraction | 1.444 |
| Symbol |
GHS07 |
|---|---|
| Signal Word | Warning |
| Hazard Statements | H302 |
| Hazard Codes | Xn |
| Risk Phrases | 22-51 |
| Safety Phrases | 20/21-29/56 |
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3 |
| HS Code | 2924199090 |
|
~35%
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| Literature: Vidal, Joelle; Damestoy, Stephanie; Guy, Laure; Hannachi, Jean-Christophe; Aubry, Andre; Collet, Andre Chemistry - A European Journal, 1997 , vol. 3, # 10 p. 1691 - 1709 |
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| Literature: Muenster, Peter; Steglich, Wolfgang Synthesis, 1987 , # 3 p. 223 - 225 |
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| Literature: Ducho, Christian; Hamed, Refaat B.; Batchelar, Edward T.; Sorensen, John L.; Odell, Barbara; Schofield, Christopher J. Organic and Biomolecular Chemistry, 2009 , vol. 7, # 13 p. 2770 - 2779 |
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| Literature: Chemistry - A European Journal, , vol. 3, # 10 p. 1691 - 1709 |
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| Literature: Chemistry - A European Journal, , vol. 3, # 10 p. 1691 - 1709 |
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| Literature: Chemistry - A European Journal, , vol. 3, # 10 p. 1691 - 1709 |
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| Literature: Tetrahedron Letters, , vol. 36, # 48 p. 8857 - 8858 |
| Precursor 10 | |
|---|---|
| DownStream 6 | |
| HS Code | 2924199090 |
|---|---|
| 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% |