(S)-ALPHA-TERT.-BUTOXYCARBONYLAMINO-BETA-(2-AMINOPYRIMIDIN-4-YL)-PROPANOIC-ACID-ALPHA-TERT.-BUTYLESTER
Compound with spectra: 1 NMR
| SpectraBase Compound ID | ItqwWgXeBZM |
|---|---|
| InChI | InChI=1S/C16H26N4O4/c1-15(2,3)23-12(21)11(20-14(22)24-16(4,5)6)9-10-7-8-18-13(17)19-10/h7-8,11H,9H2,1-6H3,(H,20,22)(H2,17,18,19)/t11-/m1/s1 |
| InChIKey | TYMYDGSJMREAMR-LLVKDONJSA-N |
| Mol Weight | 338.41 g/mol |
| Molecular Formula | C16H26N4O4 |
| Exact Mass | 338.195405 g/mol |
| Enantiomer InChIKey | TYMYDGSJMREAMR-NSHDSACASA-N |
| Racemate InChIKey | TYMYDGSJMREAMR-UHFFFAOYSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
N-(TERT.-BUTYLOXYCARBONYL)-L-3-BROMOTYROSINE-TERT.-BUTYLESTER
N(A)-T-Butoxycarbonyl-N(im)-(2-cyano-ethyl)-L-histidine methyl ester
(S)-ALPHA-TERT.-BUTOXYCARBONYLAMINO-GAMMA-(2-AMINO-6-PROPYLPYRIMIDIN-4-YL)-BUTYRIC-ACID-ALPHA-TERT.-BUTYLESTER
1-[(BENZYLOXY)METHYL]-N-CARBOXY-L-HISTIDINE, N-tert-BUTYL ESTER
3-Nitro-N-[[(phenylmethoxy)carbonyl]-L-tyrosine 1,1-dimethylethyl ester
(S)-ALPHA-TERT.-BUTOXYCARBONYLAMINO-GAMMA-(2-METHYL-6-PROPYLPYRIMIDIN-4-YL)-BUTYRIC-ACID-ALPHA-TERT.-BUTYLESTER
1-TERT.-BUTYL-5-METHYL-(2S)-N-TERT.-BUTOXYCARBONYL-4-PROPYLIDENEGLUTAMATE
METHYL-1-[(2S)-3-TERT.-BUTOXY-2-(TERT.-BUTOXYCARBONYLAMINO)-3-OXOPROPYL]-CYCLOPROPANECARBOXYLATE
(R)-METHYL-3-(3-CHLORO-4-METHOXYPHENYL)-2-(TERT.-BUTOXYCARBONYLAMINO)-PROPANOATE
Ethyl-N-(3,4,4-trimethyl-1,2-dioxetane-3-ylmethoxycarbonyl)-L-phenylalanate
| Title | Journal or Book | Year |
|---|---|---|
| The synthesis of pyrimidin-4-yl substituted α-amino acids. A versatile approach from alkynyl ketones | Journal of the Chemical Society, Perkin Transactions 1 | 1999 |
KnowItAll NMR Spectral Library
Author: Wiley
The KnowItAll NMR Spectral Library offers a comprehensive collection of NMR reference spectra, including NMR, CNMR, and XNMR, and covers a wide range of compounds including organics, polymers, monomers, metabolites, and more. Learn more.