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Merck
CN

A7331

trans-2-Aminocyclohexanecarboxylic acid

≥97% (titration)

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About This Item

Empirical Formula (Hill Notation):
C7H13NO2
CAS Number:
Molecular Weight:
143.18
UNSPSC Code:
12352200
Beilstein/REAXYS Number:
3196018
MDL number:
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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

SMILES string

N[C@@H]1CCCC[C@H]1C(O)=O

InChI key

USQHEVWOPJDAAX-PHDIDXHHSA-N

assay

≥97% (titration)

mp

~255 °C (dec.)

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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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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
Nóra V Nagy et al.
Inorganic chemistry, 51(3), 1386-1399 (2012-01-10)
With the aim of an improved understanding of the metal-complexation properties of alicyclic β-amino acid stereoisomers, and their peptides, the complex equilibria and modes of coordination with copper(II) of L-phenylalanine (F) derivatives of cis/trans-2-aminocyclohexanecarboxylic acid (c/tACHC), i.e. the dipeptides F-c/tACHC
D H Appella et al.
Nature, 387(6631), 381-384 (1997-05-22)
Proteins and RNA are unique among known polymers in their ability to adopt compact and well-defined folding patterns. These two biopolymers can perform complex chemical operations such as catalysis and highly selective recognition, and these functions are linked to folding
Ulf Strijowski et al.
Organic & biomolecular chemistry, 2(8), 1105-1109 (2004-04-06)
A series of cyclic peptides containing either cis- or trans-2-aminocyclohexane carboxylic acid as mimics for L-proline has been synthesized and their structural properties have been investigated using NMR and MD methods.
Betas are brought into the fold.
B L Iverson
Nature, 385(6612), 113-113 (1997-01-09)

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