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CAS 914349-27-2

:

1,1-Dimethylethyl 3-iodo-4-(phenylmethoxy)-1H-indole-1-carboxylate

Description:
1,1-Dimethylethyl 3-iodo-4-(phenylmethoxy)-1H-indole-1-carboxylate, with the CAS number 914349-27-2, is a chemical compound that belongs to the indole family, characterized by its complex structure featuring an indole ring system. This compound contains a carboxylate functional group, which contributes to its potential reactivity and solubility properties. The presence of the iodo substituent enhances its electrophilic character, making it useful in various synthetic applications. Additionally, the phenylmethoxy group can influence the compound's lipophilicity and biological activity. Typically, compounds of this nature may exhibit interesting pharmacological properties, making them subjects of interest in medicinal chemistry. The steric hindrance introduced by the dimethyl group can affect the compound's conformation and interactions with biological targets. Overall, this compound's unique structural features suggest potential utility in research and development, particularly in the fields of drug discovery and organic synthesis.
Formula:C20H20INO3
InChI:InChI=1S/C20H20INO3/c1-20(2,3)25-19(23)22-12-15(21)18-16(22)10-7-11-17(18)24-13-14-8-5-4-6-9-14/h4-12H,13H2,1-3H3
InChI key:InChIKey=FPBWYSDCTPHCSY-UHFFFAOYSA-N
SMILES:C(OC(C)(C)C)(=O)N1C=2C(=C(OCC3=CC=CC=C3)C=CC2)C(I)=C1
Synonyms:
  • 1,1-Dimethylethyl 3-iodo-4-(phenylmethoxy)-1H-indole-1-carboxylate
  • 1H-Indole-1-carboxylic acid, 3-iodo-4-(phenylmethoxy)-, 1,1-dimethylethyl ester
  • FPBWYSDCTPHCSY-UHFFFAOYSA-N
  • 4-(Benzyloxy)-3-iodo-1H-indole,N-BOCprotected98%
  • 4-(Benzyloxy)-3-iodo-1H-indole, N-BOC protected 98%
  • tert-Butyl 4-(benzyloxy)-3-iodo-1H-indole-1-carboxylate, 4-(Benzyloxy)-1-(tert-butoxycarbonyl)-3-iodo-1H-indole
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