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2-Aminocyclohexanecarboxylic acid hydrochloride
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2-Aminocyclohexanecarboxylic acid hydrochloride

CAS: 5691-19-0

Ref. 3D-FA130874

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Estimated delivery in United States, on Tuesday 28 Jan 2025

Product Information

Name:
2-Aminocyclohexanecarboxylic acid hydrochloride
Synonyms:
  • cyclohexanecarboxylic acid
  • 2-amino-
  • hydrochloride
  • (±)-trans-2-Aminocyclohexanecarboxylic acid
  • 1,2-trans-Aminocyclohexanecarboxylic acid
  • Cyclohexanecarboxylic acid, 2-amino-, (1R,2R)-rel-
  • Cyclohexanecarboxylic acid, 2-amino-, trans-
  • cyclohexanecarboxylic acid, 2-amino-, (1R,2R)-
  • rel-(1R,2R)-2-Aminocyclohexanecarboxylic acid
  • trans-2-Aminocyclohexane-1-carboxylic acid
  • See more synonyms
  • trans-Hexahydroanthranilic acid
Description:

2-Aminocyclohexanecarboxylic acid hydrochloride is a sequence of amino acids with a protonated amide group. The conformational properties and hemolytic activity of 2-aminocyclohexanecarboxylic acid hydrochloride are determined by the stereoselective and asymmetric synthesis, which involves the formation of an amide bond between the carboxylic acid and the amino group. This compound has been shown to be a molecular target for peptides that bind to β-amino acids. Molecular modeling studies have confirmed that 2-aminocyclohexanecarboxylic acid hydrochloride is capable of forming hydrogen bonds with nitro groups.
2-Aminocyclohexanecarboxylic acid hydrochloride is used in protein binding experiments. It is also used as an intermediate in the synthesis of other compounds.

Notice:
Our products are intended for lab use only. For any other use, please contact us.
Brand:
Biosynth
Long term storage:
Notes:

Chemical properties

Molecular weight:
143.18 g/mol
Formula:
C7H13NO2
Purity:
Min. 95%
InChI:
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:
InChIKey=USQHEVWOPJDAAX-PHDIDXHHSA-N
SMILES:
N[C@@H]1CCCC[C@H]1C(=O)O
MDL:
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EINECS:
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HS code:

Hazard Info

UN Number:
EQ:
Class:
H Statements:
P Statements:
Forbidden to fly:
Hazard Info:
Packing Group:
LQ:

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