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Structure

Fmoc-(2S,3R)-3-phenylpyrrolidine-2-carboxylic acid

CAS
281655-32-1
Catalog Number
ACM281655321
Category
Amino Acids
Molecular Weight
413.5
Molecular Formula
C26H23NO4

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Specification

Description
Fmoc-(2S,3R)-3-phenylpyrrolidine-2-carboxylic acid is a type of amino acid derivative that is mostly utilized in the field of organic synthesis for the production of peptides and peptidomimetics. The term Fmoc refers to the fluorenylmethyloxycarbonyl protecting group which allows for the selective protection and deprotection of the amino group in the synthesis of peptides.
Synonyms
FMOC-(2S,3R)-3-PHENYLPYRROLIDINE-2-CARBOXYLIC ACID
IUPAC Name
(2S,3R)-1-(9H-fluoren-9-ylmethoxycarbonyl)-3-phenylpyrrolidine-2-carboxylic acid
Canonical SMILES
C1CN(C(C1C2=CC=CC=C2)C(=O)O)C(=O)OCC3C4=CC=CC=C4C5=CC=CC=C35
InChI
1S/C26H23NO4/c28-25(29)24-18(17-8-2-1-3-9-17)14-15-27(24)26(30)31-16-23-21-12-6-4-10-19(21)20-11-5-7-13-22(20)23/h1-13,18,23-24H,14-16H2,(H,28,29)/t18-,24+/m1/s1
InChI Key
XZINBBVSLWSWBO-KOSHJBKYSA-N
Application
Fmoc-(2S,3R)-3-phenylpyrrolidine-2-carboxylic acid is mainly used in the field of organic synthesis for the production of peptides and peptidomimetics. The compound is a building block for the synthesis of peptide-based compounds with potential therapeutic applications in the treatment of diseases such as cancer, infectious diseases, and autoimmune disorders.
Exact Mass
413.163
Functional Group
Fmoc
LogP
4.8161
MDL Number
MFCD01860724
PSA
66.84
Storage Temperature
4 ℃
Type
Unusual Amino Acids, Analogs of Proline
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