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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(3-(tert-butoxycarbonyl)phenyl)propanoic acid
For research use only. Not for therapeutic Use.
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(3-(tert-butoxycarbonyl)phenyl)propanoic acid(CAT: L000265) is a key compound with applications in pharmaceutical chemistry. This chiral molecule plays a vital role in the development of drug candidates. Its action method involves selectively binding to specific biological targets, making it crucial for the synthesis of enantiomerically pure drugs. It finds applications in the pharmaceutical industry for the creation of potent and safer medications, especially in the context of chiral drug design and development.
Catalog Number | L000265 |
CAS Number | 210282-33-0 |
Molecular Formula | C29H29NO6 |
Purity | ≥95% |
IUPAC Name | (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-[3-[(2-methylpropan-2-yl)oxycarbonyl]phenyl]propanoic acid |
InChI | InChI=1S/C29H29NO6/c1-29(2,3)36-27(33)19-10-8-9-18(15-19)16-25(26(31)32)30-28(34)35-17-24-22-13-6-4-11-20(22)21-12-5-7-14-23(21)24/h4-15,24-25H,16-17H2,1-3H3,(H,30,34)(H,31,32)/t25-/m0/s1 |
InChIKey | XHBQLWKTRQMTPQ-VWLOTQADSA-N |