Fortfahren mit
07618
trans-2-Amino-cyclohexancarbonsäure
≥97.0%
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Über diesen Artikel
Empirische Formel (Hill-System):
C7H13NO2
CAS-Nummer:
Molekulargewicht:
143.18
UNSPSC Code:
12352106
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
3196018
Quality Segment
assay
≥97.0%
form
powder
reaction suitability
reaction type: solution phase peptide synthesis
color
white to faint beige
mp
~255 °C (dec.)
application(s)
peptide synthesis
SMILES string
N[C@@H]1CCCC[C@H]1C(O)=O
InChI
1S/C7H13NO2/c8-6-4-2-1-3-5(6)7(9)10/h5-6H,1-4,8H2,(H,9,10)/t5-,6-/m1/s1
InChI key
USQHEVWOPJDAAX-PHDIDXHHSA-N
Lagerklasse
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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William C Pomerantz et al.
Journal of the American Chemical Society, 133(34), 13604-13613 (2011-08-06)
We have examined the effect of β-peptide modifications on the propensity of these helical molecules to form lyotropic liquid crystalline (LC) phases in water. All of the β-peptides we have examined contain 10 residues. In each case, at least three
Matthew G Woll et al.
Journal of the American Chemical Society, 124(42), 12447-12452 (2002-10-17)
A stereoselective synthetic route is reported for the introduction of side chains at the 3-position of trans-2-aminocyclopentanecarboxylic acid (ACPC). Ring opening of the aziridine 2-benzyloxymethyl-6-azabicyclo[3.1.0]hexane with selected nucleophiles occurs in a regioselective manner and provides ACPC precursors with functional groups
Anasztázia Hetényi et al.
Journal of the American Chemical Society, 127(2), 547-553 (2005-01-13)
Homo-oligomers constructed by using trans-2-aminocyclohexanecarboxylic acid monomers without protecting groups were studied. Both ab initio theory and NMR measurements showed that the tetramer tends to adopt a 10-helix motif, while the pentamer and hexamer form the known 14-helix. It was
Global Trade Item Number
| SKU | GTIN |
|---|---|
| E49304-25G | 04061832425801 |
| 07618-500MG | 04061832593210 |