CAS 76969-87-4

Butanoic acid, 4-bromo-2-[[(1,1-dimethylethoxy)carbonyl]amino]-,methyl ester, (2S)-

Description:

Butanoic acid, 4-bromo-2-[[(1,1-dimethylethoxy)carbonyl]amino]-, methyl ester, with the CAS number 76969-87-4, is a chemical compound characterized by its complex structure that includes a butanoic acid moiety, a bromo substituent, and a methyl ester functional group. This compound features a chiral center, indicating that it exists in two enantiomeric forms, with the (2S)- configuration being specified. The presence of the 1,1-dimethylethoxycarbonyl group suggests that it may be used in synthetic organic chemistry, particularly in the context of peptide synthesis or as an intermediate in the preparation of more complex molecules. The bromo substituent can serve as a site for further chemical reactions, such as nucleophilic substitutions. Overall, this compound is likely to exhibit properties typical of carboxylic acid derivatives, including solubility in organic solvents and potential reactivity under various chemical conditions. Its specific applications would depend on its reactivity and the functional groups present in its structure.

Formula: C₁₀H₁₈BrNO₄

Methyl (S)-2-(Boc-amino)-4-bromobutyrate

CAS: 76969-87-4

Formula: C₁₀H₁₈BrNO₄

Purity: 96%

Color and Shape: Solid

Molecular weight: 296.1582

Ref: IN-DA00G9A9

Methyl (S)-2-(Boc-amino)-4-bromobutyrate

CAS: 76969-87-4

Methyl (S)-2-(Boc-amino)-4-bromobutyrate

Purity: 99%

Molecular weight: 296.161g/mol

Ref: 54-OR73323

Methyl (S)-2-(Boc-amino)-4-bromobutyrate

CAS: 76969-87-4

Purity: 96%

Molecular weight: 296.1610107

Ref: 10-F689851

Methyl (S)-2-(boc-amino)-4-bromobutyrate

CAS: 76969-87-4

Methyl (S)-2-(boc-amino)-4-bromobutyrate is a methyl ester of glycine. It can be synthesized from ethylene and acid methyl bromide in the presence of a base. The resulting product, 2-(boc-amino)-4-bromobutyrate, can be alkylated with methyl iodide to yield Methyl (S)-2-(boc-amino)-4-bromobutyrate. This compound has been shown to inhibit the activity of pharmacological regulators such as heteroduplexes, homopurine, and solid phase nucleic acid sequences. Methyl (S)-2-(boc-amino)-4-bromobutyrate also inhibits the synthesis of DNA chains and analogues.

Formula: C₁₀H₁₈BrNO₄

Purity: Min. 95%

Molecular weight: 296.16 g/mol

Ref: 3D-BDA96987