CAS 1146954-88-2: ethyl (2R)-3-hydroxy-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoate

Description: Ethyl (2R)-3-hydroxy-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoate, identified by its CAS number 1146954-88-2, is an organic compound characterized by its ester functional group and a chiral center at the second carbon atom. This compound features a hydroxy group, which contributes to its potential solubility in polar solvents, and an amino group that is protected by a bulky tert-butoxycarbonyl (Boc) moiety, enhancing its stability and reactivity in synthetic applications. The presence of the ethyl ester indicates that it can undergo hydrolysis, making it useful in various chemical reactions, including those in medicinal chemistry and organic synthesis. Its stereochemistry is significant, as the (2R) configuration can influence biological activity and interactions with enzymes or receptors. Overall, this compound is of interest in the fields of pharmaceuticals and organic synthesis due to its structural complexity and functional groups that allow for further chemical modifications.

Formula: C₁₀H₁₉NO₅

Synonyms:

• (R)-Ethyl 2-((tert-butoxycarbonyl)amino)-3-hydroxypropanoate
• N-[(1,1-Dimethylethoxy)carbonyl]-D-serine ethyl ester
• X9092

D-Serine, N-[(1,1-dimethylethoxy)carbonyl]-, ethyl ester

CAS: 1146954-88-2

• Formula: C₁₀H₁₉NO₅
• Purity: 95%
• Color and Shape: Solid
• Molecular weight: 233.2616

(R)-Ethyl 2-((tert-butoxycarbonyl)amino)-3-hydroxypropanoate

CAS: 1146954-88-2

• Purity: 95.0%
• Color and Shape: Solid
• Molecular weight: 233.26400756835938

(R)-Ethyl 2-((tert-butoxycarbonyl)amino)-3-hydroxypropanoate

CAS: 1146954-88-2

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• Formula: C₁₀H₁₉NO₅
• Purity: Min. 95%
• Molecular weight: 233.26 g/mol