CAS 196707-32-1

(R)-N-BOC-4-Fluorophenylglycine

Description:

(R)-N-BOC-4-Fluorophenylglycine is a chiral amino acid derivative characterized by its unique structural features. The compound contains a fluorinated phenyl group, which enhances its biological activity and potential applications in medicinal chemistry. The BOC (tert-butyloxycarbonyl) protecting group on the nitrogen atom provides stability and facilitates further chemical modifications. This compound is typically used in the synthesis of peptides and other bioactive molecules due to its ability to introduce chirality and functional diversity. Its fluorine atom can influence the compound's lipophilicity and binding interactions, making it valuable in drug design. Additionally, (R)-N-BOC-4-Fluorophenylglycine is often utilized in research settings to study the effects of fluorinated amino acids on protein structure and function. As with many chemical substances, proper handling and storage are essential to maintain its integrity and ensure safety during use.

Formula: C₁₃H₁₅FNO₄

InChI: InChI=1/C13H16FNO4/c1-13(2,3)19-12(18)15-10(11(16)17)8-4-6-9(14)7-5-8/h4-7,10H,1-3H3,(H,15,18)(H,16,17)/p-1/t10-/m1/s1

Synonyms:

• (D)-N-tert-Butoxycarbonyl-alpha-(4-fluorophenyl)acetic acid
• (2R)-[(tert-butoxycarbonyl)amino](4-fluorophenyl)ethanoate

Benzeneacetic acid, a-[[(1,1-dimethylethoxy)carbonyl]amino]-4-fluoro-,(aR)-

CAS: 196707-32-1

Formula: C₁₃H₁₆FNO₄

Purity: 98%

Color and Shape: Solid

Molecular weight: 269.2688

Ref: IN-DA00I3KY

(R)-2-((tert-butoxycarbonyl)amino)-2-(4-fluorophenyl)acetic acid

CAS: 196707-32-1

(R)-2-((tert-butoxycarbonyl)amino)-2-(4-fluorophenyl)acetic acid

Purity: 98%

Ref: 54-PC1008523

(R)-2-((tert-butoxycarbonyl)amino)-2-(4-fluorophenyl)acetic acid

CAS: 196707-32-1

Purity: 98%

Molecular weight: 269.2720032

Ref: 10-F771611