Skip to Content
Merck

Key Documents

View All Documentation

A7331

trans-2-Aminocyclohexanecarboxylic acid

≥97% (titration)

Sign In to View Organizational & Contract Pricing.

Select a Size

Change View

About This Item

Empirical Formula (Hill Notation):
C7H13NO2
CAS Number:
5691-19-0
Molecular Weight:
143.18
UNSPSC Code:
12352200
Beilstein/REAXYS Number:
3196018
MDL number:
MFCD00145418
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

assay

≥97% (titration)

mp

~255 °C (dec.)

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

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)

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
126H2505
065H2632
062K2512
020K2519
129H2512

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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
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
View All Related Papers