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F6312

Fmoc-(S)-2-(4-pentenyl)Ala-OH

Name: Fmoc-(<I>S</I>)-2-(4-pentenyl)Ala-OH
Brand: ALDRICH

≥97%, for peptide synthesis

Synonym(s):

(S)-N-Fmoc-α-4-n-pentenylalanine, Fmoc-(S)-2-(4-pentenyl)alanine, Fmoc-(S)-2-amino-2-methyl-hept-6-enoic acid

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About This Item

Empirical Formula (Hill Notation):

C₂₃H₂₅NO₄

CAS Number:

288617-73-2

Molecular Weight:

379.45

MDL number:

MFCD09879888

UNSPSC Code:

12352209

NACRES:

NA.26

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Properties

Product Name

Fmoc-(S)-2-(4-pentenyl)Ala-OH, ≥97%

assay

≥97%

form

solid

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

mp

<30 °C

application(s)

peptide synthesis

functional group

Fmoc

storage temp.

−20°C

SMILES string

N([C@](CCCC=C)(C)C(=O)O)C(=O)OCC1c2c(cccc2)c3c1cccc3

InChI

1S/C23H25NO4/c1-3-4-9-14-23(2,21(25)26)24-22(27)28-15-20-18-12-7-5-10-16(18)17-11-6-8-13-19(17)20/h3,5-8,10-13,20H,1,4,9,14-15H2,2H3,(H,24,27)(H,25,26)/t23-/m0/s1

InChI key

MRJFPZWLOJOINV-QHCPKHFHSA-N

Description

Application

Fmoc-(S)-2-(4-pentenyl)Ala-OH is a Fmoc-protected amino acid that can be used to create peptide libraries.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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Z-selective olefin metathesis on peptides: Investigation of side chain influence, preorganization, and guidelines in substrate selection.

O?Leary D J and Grubbs R H

Amino Acids, 5, S13-S13 null

Synthesis of all-hydrocarbon stapled α-helical peptides by ring-closing olefin metathesis.

Young-Woo Kim et al.

Nature protocols, 6(6), 761-771 (2011-06-04)

This protocol provides a detailed procedure for the preparation of stapled α-helical peptides, which have proven their potential as useful molecular probes and as next-generation therapeutics. Two crucial features of this protocol are (i) the construction of peptide substrates containing

Global Trade Item Number

SKU	GTIN
F6312-1G	04061833618608
F6312-5G	04061832597782