Chemical Forums
Specialty Chemistry Forums => Biochemistry and Chemical Biology Forum => Topic started by: evarain on July 24, 2006, 10:01:46 PM
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:(dear all
can anybody tell me how to stay the hydrolyze of 2-chloro-4-nitrophenyl-N-acetyl-?-D-glucosaminide ?(a sort of substrate of indican) i was worried along att his problem.please help me ???
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It's just a removal of the 2-chloro-nitrophenyl group from the anomeric carbon (carbon #1) of the N-acetyl-glucosamine.
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thanks?but are there any other methods?i must use 2-chloro-4-nitrophenyl-N-acetyl-?-D-glucosaminide as sustrate