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CAS 168169-11-7

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N-Boc-1-amino-4-bromonaphthalene

Description:
N-Boc-1-amino-4-bromonaphthalene is a chemical compound characterized by its naphthalene backbone, which features a bromine atom and an amino group at specific positions on the aromatic rings. The "N-Boc" designation indicates that the amino group is protected by a tert-butyloxycarbonyl (Boc) group, which is commonly used in organic synthesis to temporarily mask amines. This protection allows for selective reactions without interference from the amino group. The compound is typically a solid at room temperature and is soluble in organic solvents such as dichloromethane and dimethyl sulfoxide. Its structure makes it useful in various synthetic applications, particularly in the development of pharmaceuticals and agrochemicals. The presence of the bromine atom also provides a site for further functionalization, making it a versatile intermediate in organic synthesis. Safety precautions should be taken when handling this compound, as it may pose health risks typical of brominated organic compounds.
Formula:C15H16BrNO2
InChI:InChI=1/C15H16BrNO2/c1-15(2,3)19-14(18)17-13-9-8-12(16)10-6-4-5-7-11(10)13/h4-9H,1-3H3,(H,17,18)
SMILES:CC(C)(C)OC(=O)Nc1ccc(c2ccccc12)Br
Synonyms:
  • 1-Boc-Amino-4-Bromonaphthalene
  • Tert-Butyl 4-Bromonaphthalen-1-Ylcarbamate
  • 1-Amino-4-bromonaphthalene, N-BOC protected
  • Carbamic acid, (4-bromo-1-naphthalenyl)-, 1,1-dimethylethyl ester
  • 1-Amino-4-bromonaphthalene, N-BOC protected 98%
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