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Atomfair (R)-1-((4-amino-2-bromo-5-fluorophenyl)amino)-3-(benzyloxy)propan-2-ol C16H18BrFN2O2
Description (R)-1-((4-amino-2-bromo-5-fluorophenyl)amino)-3-(benzyloxy)propan-2-ol (CAS No. 1294504-63-4) is a high-purity chiral compound with the molecular formula C16H18BrFN2O2. This specialized chemical features a unique structure combining an aromatic bromo-fluoroaniline moiety with a benzyloxypropanol group, making it a valuable intermediate for pharmaceutical research and organic synthesis. The compound is supplied as a solid with strict quality control to ensure batch-to-batch consistency, characterized by HPLC, NMR, and mass spectrometry. Its IUPAC name is (2R)-1-(4-amino-2-bromo-5-fluoroanilino)-3-phenylmethoxypropan-2-ol, and it is particularly useful for developing targeted therapies due to its stereospecific configuration and reactive functional groups.
Description
Description
(R)-1-((4-amino-2-bromo-5-fluorophenyl)amino)-3-(benzyloxy)propan-2-ol (CAS No. 1294504-63-4) is a high-purity chiral compound with the molecular formula C16H18BrFN2O2. This specialized chemical features a unique structure combining an aromatic bromo-fluoroaniline moiety with a benzyloxypropanol group, making it a valuable intermediate for pharmaceutical research and organic synthesis. The compound is supplied as a solid with strict quality control to ensure batch-to-batch consistency, characterized by HPLC, NMR, and mass spectrometry. Its IUPAC name is (2R)-1-(4-amino-2-bromo-5-fluoroanilino)-3-phenylmethoxypropan-2-ol, and it is particularly useful for developing targeted therapies due to its stereospecific configuration and reactive functional groups.
- CAS No: 1294504-63-4
- Molecular Formula: C16H18BrFN2O2
- Molecular Weight: 369.23
- Exact Mass: 368.05357
- Monoisotopic Mass: 368.05357
- IUPAC Name: (2R)-1-(4-amino-2-bromo-5-fluoroanilino)-3-phenylmethoxypropan-2-ol
- SMILES: C1=CC=C(C=C1)COC[C@@H](CNC2=C(C=C(C(=C2)F)N)Br)O
- Synonyms: (R)-1-((4-amino-2-bromo-5-fluorophenyl)amino)-3-(benzyloxy)propan-2-ol, (2R)-1-(4-amino-2-bromo-5-fluoroanilino)-3-phenylmethoxypropan-2-ol, SCHEMBL352006, XFEDZKLXQZLTRU-GFCCVEGCSA-N
Application
This compound serves as a key chiral building block in medicinal chemistry, particularly for developing kinase inhibitors and targeted cancer therapies. Researchers utilize it in structure-activity relationship (SAR) studies due to its bromo-fluoro substitution pattern and amino functionality. The benzyloxypropanol moiety makes it valuable for prodrug development and solubility modification in drug discovery programs.
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