CAS 144186-13-0
:BOC-DL-CHA-OH
Description:
BOC-DL-CHA-OH, also known as Boc-DL-cyclohexylalaninol, is a chemical compound characterized by its structure that includes a tert-butyloxycarbonyl (Boc) protecting group attached to a cyclohexylalaninol moiety. This compound is typically used in organic synthesis, particularly in the preparation of peptides and other complex organic molecules, due to its ability to protect amine functionalities during chemical reactions. The presence of the cyclohexyl group contributes to its hydrophobic characteristics, influencing its solubility and reactivity. BOC-DL-CHA-OH is a chiral compound, which means it exists in two enantiomeric forms, making it relevant in the field of asymmetric synthesis. Its CAS number, 144186-13-0, allows for easy identification in chemical databases. As with many organic compounds, handling should be done with care, following appropriate safety protocols to mitigate any potential hazards associated with its use in laboratory settings.
Formula:C14H25NO4
Synonyms:- Boc-3-cyclohexyl-DL-alanine
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Found 4 products.
Boc-DL-Cha-OH
CAS:<p>Boc-DL-Cha-OH</p>Formula:C14H25NO4Purity:98%Color and Shape: off white solidMolecular weight:271.35g/molBoc-Dl-Cha-OH
CAS:<p>Boc-Dl-Cha-OH is a fluorescent compound that binds to the opioid receptor. It is not an opioid and does not produce any pain relief. Boc-Dl-Cha-OH has significant activity against Mycobacterium tuberculosis, which was shown in a study using radioligand binding, which is a technique that measures the ability of a ligand to bind to a specific receptor. The affinity of Boc-Dl-Cha-OH for the receptor was also confirmed by its ability to inhibit the growth of Mycobacterium tuberculosis in tissue culture and ethambutol. This drug also has antimicrobial properties and can be used to treat infections caused by bacteria that are resistant to other antibiotics such as penicillin, erythromycin, or tetracycline.</p>Formula:C14H25NO4Purity:Min. 95%Molecular weight:271.35 g/mol



