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47517

Sigma-Aldrich

Fmoc-Hyp(tBu)-OH

≥98.0% (HPLC)

Synonym(s):

Fmoc-O-tert-butyl-L-hydroxyproline

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About This Item

Empirical Formula (Hill Notation):
C24H27NO5
CAS Number:
122996-47-8
Molecular Weight:
409.47
Beilstein:
6161467
MDL number:
MFCD00151930
UNSPSC Code:
12352209
eCl@ss:
32160406
PubChem Substance ID:
57650984
NACRES:
NA.26

Assay

≥98.0% (HPLC)

optical activity

[α]20/D −25±2.5°, c = 1% in methanol

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

application(s)

peptide synthesis

functional group

Fmoc

storage temp.

2-8°C

SMILES string

CC(C)(C)O[C@@H]1C[C@H](N(C1)C(=O)OCC2c3ccccc3-c4ccccc24)C(O)=O

InChI

1S/C24H27NO5/c1-24(2,3)30-15-12-21(22(26)27)25(13-15)23(28)29-14-20-18-10-6-4-8-16(18)17-9-5-7-11-19(17)20/h4-11,15,20-21H,12-14H2,1-3H3,(H,26,27)/t15-,21+/m1/s1

InChI key

WPBXBYOKQUEIDW-VFNWGFHPSA-N

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Eugene Rogozhin et al.
International journal of molecular sciences, 19(11) (2018-11-08)
Herein, we describe a modified form of the antimicrobial hairpin-like peptide EcAMP1, isolated from barnyard grass (E. crusgalli) seeds, which is structurally characterized by a combination of high-pressure liquid chromatography, mass spectrometry, and automated Edman sequencing. This derivate has a
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Toxicon : official journal of the International Society on Toxinology, 130, 1-10 (2017-02-28)
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