Methyl (2R)-2-(tert-butoxycarbonylamino)-3-chloro-propanoate is a chemical compound characterized by its specific structural features, including a methyl ester group and a tert-butoxycarbonyl (Boc) protecting group attached to an amino group. This compound is typically used in organic synthesis, particularly in the preparation of amino acids and peptides. The presence of the chloro substituent on the propanoate backbone introduces reactivity that can be exploited in further chemical transformations. The Boc group serves as a protective moiety, allowing for selective reactions at other functional groups without interference. This compound is generally stable under standard laboratory conditions but should be handled with care due to the presence of chlorine, which can pose hazards. Its solubility properties may vary depending on the solvent used, and it is important to consider its reactivity in the context of the desired synthetic pathway. Overall, this compound exemplifies the complexity and utility of modified amino acid derivatives in synthetic organic chemistry.

methyl (2R)-2-(tert-butoxycarbonylamino)-3-chloro-propanoate

651035-84-6: Methyl (2R)-2-(tert-butoxycarbonylamino)-3-chloro-propanoate is a chemical compound characterized by its specific structural features, including a methyl ester group and a tert-butoxycarbonyl (Boc) protecting group attached to an amino group. This compound is typically used in organic synthesis, particularly in the preparation of amino acids and peptides. The presence of the chloro substituent on the propanoate backbone introduces reactivity that can be exploited in further chemical transformations. The Boc group serves as a protective moiety, allowing for selective reactions at other functional groups without interference. This compound is generally stable under standard laboratory conditions but should be handled with care due to the presence of chlorine, which can pose hazards. Its solubility properties may vary depending on the solvent used, and it is important to consider its reactivity in the context of the desired synthetic pathway. Overall, this compound exemplifies the complexity and utility of modified amino acid derivatives in synthetic organic chemistry.

CAS 651035-84-6

methyl (2R)-2-(tert-butoxycarbonylamino)-3-chloro-propanoate

Boc-Ser(cl)-Ome

Ref: IN-DA00EAQA

(R)-Methyl 2-((tert-butoxycarbonyl)amino)-3-chloropropanoate

Ref: 54-OR92988

METHYL N-BOC-3-CHLORO-L-ALANINATE

Ref: 10-F303282