TCI B6669, tert-Butyl 4-(4-Acetyl-2-methoxy-5-nitrophenoxy)butanoate (CAS 1410809-15-2), is the ketone counterpart within the same photolabile protecting group series, carrying acetyl, methoxy, and nitro substituents on the aromatic ring. The benzylic acetyl group offers a clear entry point for reduction to the corresponding secondary benzylic alcohol used in caging chemistry. Its tert-butyl protected butanoate arm serves as a linker toward peptides, probes, or functionalized surfaces. AMI Scientific provides this TCI reagent in a 1 g pack size for laboratory-scale synthesis and method development.
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- Smith (1997). tert-Butyl-3-methoxy-5,5-dimethyl-6-heptenoate. Molecules doi:10.3390/m30
- Smith (1997). tert-Butyl-3-methoxy-5,5-dimethyl-7-oxo-heptanoate. Molecules doi:10.3390/m32
- Smith (1997). tert-Butyl-3-methoxy-5,5-dimethyl-7-hydroxy-heptanoate. Molecules doi:10.3390/m31
References were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.
