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Merck
모든 사진(1)

주요 문서

07618

Sigma-Aldrich

trans-2-Aminocyclohexanecarboxylic acid

≥97.0%

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About This Item

실험식(Hill 표기법):
C7H13NO2
CAS Number:
Molecular Weight:
143.18
Beilstein:
3196018
MDL number:
UNSPSC 코드:
12352106
PubChem Substance ID:
NACRES:
NA.22

Quality Level

분석

≥97.0%

양식

powder

반응 적합성

reaction type: solution phase peptide synthesis

색상

white to faint beige

mp

~255 °C (dec.)

응용 분야

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

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Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

Eyeshields, Gloves, type N95 (US)


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문서 라이브러리 방문

Betas are brought into the fold.
B L Iverson
Nature, 385(6612), 113-113 (1997-01-09)
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
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
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
M Marastoni et al.
Arzneimittel-Forschung, 49(1), 6-12 (1999-02-24)
The solid phase synthesis, based on the Fmoc chemical protocol, was used to prepare ten deltorphin C (Del-C; H-Tyr-D-Ala-Phe-Asp-Val-Val-Gly-NH2) analogues containing cis- and trans- 2 or 3- or 4- aminocyclohexanecarboxylic acid (ACCA) residues at position 2. ACCA-peptides showed high resistance

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