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CAS 162356-90-3

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1,1-Dimethylethyl N-[(2-bromophenyl)methyl]carbamate

Description:
1,1-Dimethylethyl N-[(2-bromophenyl)methyl]carbamate, with the CAS number 162356-90-3, is an organic compound characterized by its carbamate functional group, which is known for its applications in agriculture and pharmaceuticals. This compound features a branched alkyl group (1,1-dimethylethyl) that contributes to its steric hindrance, potentially influencing its reactivity and interaction with biological systems. The presence of the 2-bromophenyl group introduces halogen functionality, which can enhance lipophilicity and affect the compound's biological activity. The overall structure suggests potential uses in pest control or as a biochemical agent, given the properties associated with carbamates, such as inhibition of acetylcholinesterase. Additionally, the compound's stability, solubility, and reactivity can be influenced by the steric and electronic effects of the substituents. Safety and handling considerations are essential, as with many halogenated organic compounds, due to potential toxicity and environmental impact.
Formula:C12H16BrNO2
InChI:InChI=1S/C12H16BrNO2/c1-12(2,3)16-11(15)14-8-9-6-4-5-7-10(9)13/h4-7H,8H2,1-3H3,(H,14,15)
InChI key:InChIKey=DFNZFCPEUDSNEO-UHFFFAOYSA-N
SMILES:C(NC(OC(C)(C)C)=O)C1=C(Br)C=CC=C1
Synonyms:
  • 1,1-Dimethylethyl N-[(2-bromophenyl)methyl]carbamate
  • 1-(tert-Butoxycarbonylaminomethyl)-2-bromobenzene
  • 10017 Tert-Butyl 2-Bromo Benzyl Carbamate
  • 2-(tert-Butoxycarbonylaminomethyl)bromobenzene
  • Carbamic acid, N-[(2-bromophenyl)methyl]-, 1,1-dimethylethyl ester
  • Carbamic acid, [(2-bromophenyl)methyl]-, 1,1-dimethylethyl ester
  • N-Boc-2-Bromobenzylamine
  • Tert-Butyl 2-Bromobenzylcarbamate
  • tert-Butyl (2-bromobenzyl)carbamate
  • tert-Butyl N-(2-bromobenzyl)carbamate
  • N-(tert-Butoxycarbonyl)-2-bromobenzylamine
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