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534404

N-Boc-cis-4-N-Fmoc-amino-L-proline

Name: N-Boc-cis-4-N-Fmoc-amino-<SC>L</SC>-proline
Brand: ALDRICH

97%

Synonym(s):

(2S,4S)-N-tert-Butoxycarbonyl-4-N-(9-fluorenylmethoxycarbonyl)aminopyrrolidine-2-carboxylic acid

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About This Item

Empirical Formula (Hill Notation):

C₂₅H₂₈N₂O₆

CAS Number:

174148-03-9

Molecular Weight:

452.50

NACRES:

NA.26

PubChem Substance ID:

24878036

UNSPSC Code:

12352209

MDL number:

MFCD00673782

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Properties

Quality Level

100

assay

97%

optical activity

[α]20/D -68°, c = 1 in chloroform

reaction suitability

reaction type: Boc solid-phase peptide synthesis

mp

150-154 °C (lit.)

application(s)

peptide synthesis

functional group

Boc, Fmoc

SMILES string

CC(C)(C)OC(=O)N1C[C@H](C[C@H]1C(O)=O)NC(=O)OCC2c3ccccc3-c4ccccc24

InChI

1S/C25H28N2O6/c1-25(2,3)33-24(31)27-13-15(12-21(27)22(28)29)26-23(30)32-14-20-18-10-6-4-8-16(18)17-9-5-7-11-19(17)20/h4-11,15,20-21H,12-14H2,1-3H3,(H,26,30)(H,28,29)/t15-,21-/m0/s1

InChI key

UPXRTVAIJMUAQR-BTYIYWSLSA-N

Description

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Articles

Proline Derivatives and Analogs

Proline analogues are promising candidates for tuning the biological, pharmaceutical, or physicochemical properties of naturally occuring, as well as de novo designed, linear, and, cyclic peptides.

Global Trade Item Number

SKU	GTIN
534404-1G	04061826095362