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04061

Sigma-Aldrich

1-(Fmoc-amino)cyclohexanecarboxylic acid

≥98.0% (T)

Synonym(s):

Fmoc-homocycloleucine

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About This Item

Empirical Formula (Hill Notation):
C22H23NO4
CAS Number:
162648-54-6
Molecular Weight:
365.42
Beilstein:
7887646
MDL number:
MFCD00273464
UNSPSC Code:
12352200
PubChem Substance ID:
329747866
NACRES:
NA.26

Assay

≥98.0% (T)

form

powder

color

white

mp

185-187 °C

application(s)

peptide synthesis

functional group

Fmoc

storage temp.

2-8°C

SMILES string

OC(=O)C1(CCCCC1)NC(=O)OCC2c3ccccc3-c4ccccc24

InChI

1S/C22H23NO4/c24-20(25)22(12-6-1-7-13-22)23-21(26)27-14-19-17-10-4-2-8-15(17)16-9-3-5-11-18(16)19/h2-5,8-11,19H,1,6-7,12-14H2,(H,23,26)(H,24,25)

InChI key

VCIVAWBKUQJNSX-UHFFFAOYSA-N

Other Notes

Unnatural amino acids employed for peptide libraries.

Storage Class Code

13 - Non 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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Certificates of Analysis (COA)

Lot/Batch Number
1223672V
1223672
063472/1
63472/1

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T. Lescrinier et al.
Chemistry (Weinheim An Der Bergstrasse, Germany), 4, 425-425 (1998)
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Therapeutic angiogenesis aims at improving cerebral blood flow by amplification of vascular sprouting, thus promoting tissue survival under conditions of subsequent ischemia. It remains unknown whether induced angiogenesis leads to the formation of functional vessels that indeed result in hemodynamic
A.P. Combs et al.
Journal of the American Chemical Society, 118, 287-287 (1996)

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