Structure

Boc-L-propargylglycine·DCHA

CAS
63039-49-6
Catalog Number
ACM63039496-2
Category
Amino Acids
Molecular Weight
213.2·181.3
Molecular Formula
C10H15NO4·C12H23N

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Specification

Description
Boc-L-pra-OH dcha is a chemical compound used in scientific research for its unique properties. It is an amino acid derivative that is used as a coupling agent for peptide synthesis. The term "Boc" in its name stands for tert-butyloxycarbonyl, which is a protective group used to protect the amine group of the amino acid during peptide synthesis. Boc-L-pra-OH dcha is a derivative of L-proline, which is an essential amino acid found in many proteins. This compound was first synthesized in 1998 and has since become a widely used compound in scientific research.
Synonyms
N-alpha-(t-Butyloxycarbonyl)-L-propargylglycine dicyclohexylamine
IUPAC Name
N-cyclohexylcyclohexanamine;(2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]pent-4-ynoic acid
Canonical SMILES
CC(C)(C)OC(=O)NC(CC#C)C(=O)O.C1CCC(CC1)NC2CCCCC2
InChI
1S/C12H23N.C10H15NO4/c1-3-7-11(8-4-1)13-12-9-5-2-6-10-12;1-5-6-7(8(12)13)11-9(14)15-10(2,3)4/h11-13H,1-10H2;1,7H,6H2,2-4H3,(H,11,14)(H,12,13)/t;7-/m.0/s1
InChI Key
AMKHAJIFPHJYMH-ZETCQYMHSA-N
Application
Boc-L-pra-OH dcha has various applications in scientific research, such as peptide coupling, organic synthesis, and medicinal chemistry research. It is also used as a building block in the synthesis of natural products.
Exact Mass
394.283
Functional Group
Boc
LogP
5.0108
MDL Number
MFCD01320855
PSA
87.66
Storage Temperature
4 ℃
Type
Unusual Amino Acids, Azide and Alkyne containing Amino Acids
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