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CAS 27494-47-9

:

(2R)-2-[(tert-butoxycarbonyl)amino]butanoic acid-N-cyclohexylcyclohexanamine (1:1)

Description:
The chemical substance known as (2R)-2-[(tert-butoxycarbonyl)amino]butanoic acid-N-cyclohexylcyclohexanamine (1:1) with CAS number 27494-47-9 is a compound that features both amino acid and amine functionalities. It is characterized by the presence of a tert-butoxycarbonyl (Boc) protecting group, which is commonly used in organic synthesis to protect amines during reactions. The structure includes a butanoic acid moiety, indicating it has carboxylic acid characteristics, which can participate in acid-base reactions. The cyclohexyl groups suggest a degree of steric hindrance, which may influence the compound's reactivity and solubility. This compound is likely to exhibit properties typical of amino acids, such as forming zwitterions in solution, and may have applications in pharmaceuticals or as a building block in peptide synthesis. Its specific stereochemistry (2R) indicates that it has a defined spatial arrangement, which can be crucial for biological activity. Overall, this compound's unique combination of functional groups and structural features makes it of interest in various chemical and biological contexts.
Formula:C21H40N2O4
InChI:InChI=1/C12H23N.C9H17NO4/c1-3-7-11(8-4-1)13-12-9-5-2-6-10-12;1-5-6(7(11)12)10-8(13)14-9(2,3)4/h11-13H,1-10H2;6H,5H2,1-4H3,(H,10,13)(H,11,12)/t;6-/m.1/s1
SMILES:C1CCC(CC1)NC1CCCCC1.CC[C@H](C(=O)O)N=C(O)OC(C)(C)C
Synonyms:
  • butanoic acid, 2-[[(1,1-dimethylethoxy)carbonyl]amino]-, (2R)-, compd. with N-cyclohexylcyclohexanamine (1:1)
  • N-Cyclohexylcyclohexanaminium (2R)-2-[(tert-butoxycarbonyl)amino]butanoate
  • (R)-(2-Boc-Amino)Butyric Acid Dicyclohexylamine Salt
  • Boc-D-Abu-OH・DCHA
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