CAS 293302-31-5

Bis-Boc-aminooxyacetic acid

Description:

Bis-Boc-aminooxyacetic acid is a chemical compound characterized by the presence of two Boc (tert-butyloxycarbonyl) protecting groups attached to an aminooxyacetic acid backbone. This structure imparts several notable characteristics. The Boc groups serve to protect the amino and hydroxyl functionalities, enhancing the compound's stability and solubility in organic solvents. The aminooxy group is reactive, allowing for potential applications in bioconjugation and the formation of stable linkages with aldehydes or ketones. The compound is typically used in organic synthesis and medicinal chemistry, particularly in the development of prodrugs or in the modification of biomolecules. Its molecular structure contributes to its ability to participate in various chemical reactions, including nucleophilic attacks and coupling reactions. Additionally, the presence of the carboxylic acid moiety allows for further functionalization, making it versatile in synthetic pathways. Overall, Bis-Boc-aminooxyacetic acid is a valuable intermediate in the synthesis of more complex molecules in pharmaceutical and chemical research.

Formula: C₁₂H₂₁NO₇

Synonyms:

• Aceticacid, 2-[[bis[(1,1-dimethylethoxy)carbonyl]amino]oxy]-
• Boc-Aoa-Oh
• Bis-Boc-Amino-Oxyacetic Acid

Bis-boc-aoa h2o

CAS: 293302-31-5

Formula: C₁₂H₂₁NO₇

Purity: 97%

Color and Shape: Solid

Molecular weight: 291.2976

Ref: IN-DA002Y21

((Bis((1,1-dimethylethoxy)carbonyl)amino)oxy)acetic acid

CAS: 293302-31-5

((Bis((1,1-dimethylethoxy)carbonyl)amino)oxy)acetic acid

Purity: 99%

Molecular weight: 291.30g/mol

Ref: 54-OR90535

Bis-Boc-amino-oxyacetic acid

CAS: 293302-31-5

Bis-Boc-amino-oxyacetic acid is an analog of goserelin acetate. It binds to the androgen receptor in prostate cancer cells, which leads to cytostatic effects. This drug has shown a low potency in human serum and does not bind to human serum proteins.
The uptake of Bis-Boc-amino-oxyacetic acid by prostate cancer cells was found to be significantly greater than that of goserelin acetate. The binding affinity of this drug for the androgen receptor is also lower than that of goserelin acetate, making it more selective for prostate cancer cells over other tissues.

Formula: C₁₂H₂₁NO₇

Purity: Min. 95%

Color and Shape: White Powder

Molecular weight: 291.3 g/mol

Ref: 3D-FB50723

[[Bis[(1,1-dimethylethoxy)carbonyl]amino]oxy]-acetic acid

CAS: 293302-31-5

Formula: C₁₂H₂₁NO₇

Purity: 97%

Color and Shape: Liquid, No data available.

Molecular weight: 291.3

Ref: 10-F236881