| Identification | Back Directory | [Name]
TERT-BUTOXYCARBONYLAMINO-ACETIC ACID ETHYL ESTER | [CAS]
14719-37-0 | [Synonyms]
Ethyl boc-aminoacetate
N-Boc-glycine Ethyl Ester
N-Boc-glycineethylester,95%
ethyl(tert-butoxycarbonyl)glycinate
EthylN-(tert-butoxycarbonyl)glycinate
tert-butoxycarbonylamino-acetic acid eth
Ethyl 2-(tert-butoxycarbonylaMino)acetate
Ethyl [(tert-butoxycarbonyl)amino]acetate
N-(tert-butoxycarbonyl)glycine ethyl ester
N-(tert-Butoxycarbonyl)glycine Ethyl Ester >
N-[(1,1-dimethylethoxy)carbonyl]Glycineethyl ester
2-(tert-butoxycarbonylamino)acetic acid ethyl ester
ethyl 2-[(2-methylpropan-2-yl)oxycarbonylamino]acetate
2-[(tert-butoxy-oxomethyl)amino]acetic acid ethyl ester
Glycine, N-[(1,1-diMethylethoxy)carbonyl]-, ethyl ester
ethyl 2-[(2-methylpropan-2-yl)oxycarbonylamino]ethanoate
N-(tert-Butoxycarbonyl)glycine Ethyl Ester
TERT-BUTOXYCARBONYLAMINO-ACETIC ACID ETHYL ESTER USP/EP/BP | [EINECS(EC#)]
1533716-785-6 | [Molecular Formula]
C9H17NO4 | [MDL Number]
MFCD05663720 | [MOL File]
14719-37-0.mol | [Molecular Weight]
203.24 |
| Chemical Properties | Back Directory | [Boiling point ]
97°C/0.7mmHg(lit.) | [density ]
1.053±0.06 g/cm3(Predicted) | [refractive index ]
1.4350 to 1.4390 | [storage temp. ]
under inert gas (nitrogen or Argon) at 2-8°C | [form ]
Oily Liquid | [pka]
11.18±0.46(Predicted) | [color ]
Colorless | [InChI]
InChI=1S/C9H17NO4/c1-5-13-7(11)6-10-8(12)14-9(2,3)4/h5-6H2,1-4H3,(H,10,12) | [InChIKey]
CNIBHMMDDXGDNR-UHFFFAOYSA-N | [SMILES]
C(OCC)(=O)CNC(OC(C)(C)C)=O |
| Hazard Information | Back Directory | [Uses]
Ethyl (tert-Butoxycarbonyl)glycinate is a Glycine.html" class="link-product" target="_blank">Glycine (HY-Y0966) derivative[1]. | [Synthesis]
1. A solution of di-tert-butyl dicarbonate (365 g, 1.67 mol) in tetrahydrofuran (1 L) was slowly added dropwise to a solution of tetrahydrofuran (2.5 L) containing ethyl glycinate hydrochloride (232.5 g, 1.66 mol) and triethylamine (497.5 ml, 3.57 mol) at 0 °C. 2. The reaction mixture was allowed to react for 36 hours under vigorous stirring. 3. . After completion of the reaction, the reaction mixture was filtered.4. The filtrate was concentrated under vacuum to give 329.49 g (98% yield) of ethyl N-tert-butoxycarbonylglycinate (compound 5) as a white solid. | [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. DOI:10.1080/10408398.2012.708368 |
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