CAS 1609546-50-0
:(3S)-4-Amino-3-fluoro-2-methyl-2-butanol
Description:
(3S)-4-Amino-3-fluoro-2-methyl-2-butanol is an organic compound characterized by its chiral center, which contributes to its specific stereochemistry. The presence of an amino group (-NH2) indicates that it can participate in various chemical reactions, including nucleophilic substitutions and coupling reactions. The fluorine atom introduces unique reactivity and polarity, potentially influencing the compound's interaction with biological systems. The methyl group and the butanol structure suggest that it is a secondary alcohol, which can undergo oxidation or dehydration reactions. This compound may exhibit solubility in polar solvents due to the hydroxyl group, while the fluorine atom can enhance its lipophilicity. Its stereochemistry may also affect its biological activity, making it of interest in pharmaceutical applications. Overall, (3S)-4-Amino-3-fluoro-2-methyl-2-butanol presents a combination of functional groups that can be exploited in synthetic chemistry and medicinal chemistry for the development of new therapeutic agents.
Formula:C5H12FNO
InChI:InChI=1S/C5H12FNO/c1-5(2,8)4(6)3-7/h4,8H,3,7H2,1-2H3/t4-/m0/s1
InChI key:InChIKey=QNFKDKWENVIYDB-BYPYZUCNSA-N
SMILES:[C@@H](C(C)(C)O)(CN)F
Synonyms:- (S)-4-Amino-3-fluoro-2-methylbutan-2-ol
- (3S)-4-Amino-3-fluoro-2-methyl-2-butanol
- (3S)-4-Amino-3-fluoro-2-methylbutan-2-ol
- 2-Butanol, 4-amino-3-fluoro-2-methyl-, (3S)-
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