04061
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:
Molecular Weight:
365.42
UNSPSC Code:
12352200
NACRES:
NA.26
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
7887646
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
SMILES string
OC(=O)C1(CCCCC1)NC(=O)OCC2c3ccccc3-c4ccccc24
assay
≥98.0% (T)
form
powder
color
white
mp
185-187 °C
application(s)
peptide synthesis
functional group
Fmoc
storage temp.
2-8°C
Other Notes
Unnatural amino acids employed for peptide libraries.
Storage Class
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
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T. Lescrinier et al.
Chemistry (Weinheim An Der Bergstrasse, Germany), 4, 425-425 (1998)
A.P. Combs et al.
Journal of the American Chemical Society, 118, 287-287 (1996)
Anil Zechariah et al.
Stroke, 44(6), 1690-1697 (2013-05-02)
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
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