CAS 33645-24-8
:benzyl L-threoninate hydrochloride
Description:
Benzyl L-threoninate hydrochloride is a chemical compound characterized by its structure, which includes a benzyl group attached to the amino acid L-threonine. It is typically encountered as a hydrochloride salt, which enhances its solubility in water and makes it more stable for various applications. This compound is often used in biochemical research and pharmaceutical formulations due to its potential role as a chiral building block in organic synthesis. The presence of the threonine moiety contributes to its biological activity, as amino acids are fundamental in various metabolic processes. In terms of physical properties, benzyl L-threoninate hydrochloride is usually a white to off-white crystalline powder. It is important to handle this compound with care, following appropriate safety protocols, as with any chemical substance. Its applications may extend to studies in drug development, particularly in the context of amino acid derivatives and their interactions in biological systems.
Formula:C11H16ClNO3
InChI:InChI=1/C11H15NO3.ClH/c1-8(13)10(12)11(14)15-7-9-5-3-2-4-6-9;/h2-6,8,10,13H,7,12H2,1H3;1H/t8-,10+;/m1./s1
Synonyms:- Benzyl L-threoninate hydrochloride (1:1)
- L-threonine, phenylmethyl ester, hydrochloride (1:1)
- H-Thr-OBzl・HCl
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Found 5 products.
L-Threonine Benzyl Ester Hydrochloride
CAS:Formula:C11H15NO3·HClPurity:>98.0%(HPLC)(N)Color and Shape:White to Almost white powder to crystalMolecular weight:245.70L-Threonine benzyl ester HCl
CAS:Formula:C11H16ClNO3Purity:98%Color and Shape:SolidMolecular weight:245.7026L-Threonine benzyl ester hydrochloride
CAS:<p>L-Threonine benzyl ester hydrochloride</p>Purity:98%Molecular weight:245.70g/molL-Threonine benzyl ester hydrochloride
CAS:<p>L-Threonine benzyl ester hydrochloride is a glycopeptide that is used as a precursor to L-threonine. It is synthesized from cycloserine, which contains a phenyl group, and D-serine, which contains an amino acid with two threonine molecules. The synthesis starts with the activation of the benzyl ester by treatment with hydrazoic acid. This activated compound reacts with D-serine in the presence of an organic base to form the benzyl ester of D-serine. The reaction can be carried out in one pot without isolation steps. The final step is an oxidative cleavage of the benzyl group by irradiation with ultraviolet light or exposure to hydrogen peroxide, yielding L-threonine benzyl ester hydrochloride as a white solid.</p>Formula:C11H15NO3•HClPurity:Min. 95%Color and Shape:White To Off-White SolidMolecular weight:245.7 g/mol(2S,3R)-Benzyl 2-amino-3-hydroxybutanoate hydrochloride
CAS:Formula:C11H16ClNO3Purity:98%Color and Shape:Solid, White - Almost white powderMolecular weight:245.7




