CAS 86938-17-2
:1-Ethyl hydrogen N-[(1,1-dimethylethoxy)carbonyl]-L-glutamate
Description:
1-Ethyl hydrogen N-[(1,1-dimethylethoxy)carbonyl]-L-glutamate, with the CAS number 86938-17-2, is an amino acid derivative that features a glutamate backbone modified with an ethyl group and a tert-butoxycarbonyl (Boc) protecting group. This compound is characterized by its ability to participate in peptide synthesis and other organic reactions due to the presence of both an amino group and a carboxylic acid functional group. The ethyl substitution enhances its lipophilicity, potentially affecting its solubility and reactivity in various solvents. The Boc group serves as a protective moiety, allowing for selective reactions while preventing unwanted side reactions during synthesis. This compound is typically used in the field of medicinal chemistry and peptide synthesis, where it can act as an intermediate or building block for more complex molecules. Its stability under standard laboratory conditions makes it a valuable reagent in organic synthesis. Overall, the unique structural features of this compound contribute to its utility in chemical research and development.
Formula:C12H21NO6
InChI:InChI=1S/C12H21NO6/c1-5-18-10(16)8(6-7-9(14)15)13-11(17)19-12(2,3)4/h8H,5-7H2,1-4H3,(H,13,17)(H,14,15)/t8-/m0/s1
InChI key:InChIKey=LXQBXYDPJVHNPQ-QMMMGPOBSA-N
SMILES:[C@@H](NC(OC(C)(C)C)=O)(C(OCC)=O)CCC(O)=O
Synonyms:- 1-Ethyl hydrogen N-[(1,1-dimethylethoxy)carbonyl]-L-glutamate
- L-Glutamic acid, N-[(1,1-dimethylethoxy)carbonyl]-, 1-ethyl ester
- (S)-4-((tert-Butoxycarbonyl)amino)-5-ethoxy-5-oxopentanoicacid
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Found 3 products.
(S)-4-((tert-Butoxycarbonyl)amino)-5-ethoxy-5-oxopentanoic acid
CAS:Formula:C12H21NO6Purity:97%Molecular weight:275.2982(S)-4-((tert-Butoxycarbonyl)amino)-5-ethoxy-5-oxopentanoic acid
CAS:(S)-4-((tert-Butoxycarbonyl)amino)-5-ethoxy-5-oxopentanoic acidPurity:95%Molecular weight:275.3g/molBoc-Glu-OEt·DCHA
CAS:Boc-Glu-OEt·DCHA is an activating, acid ethyl ester of diazoalkane. It is used as a reagent in organic synthesis and has been used to activate the carboxyl group of an active ester. The reactivity of the boc group has been shown by the formation of an intramolecular ester bond with the ethyl acetate molecule. The reaction scheme for this process is shown below:Formula:C12H21NO6·C12H23NPurity:Min. 95%Molecular weight:456.62 g/mol


