1010809-58-1

Basic information

• Product Name: (2S,3R,4S)-1-(N,N'-dibenzylamidino)-3,4,5,5-tetrahydroxy-2-hydroxymethylpiperidine hydrochloride
• Synonyms: (2S,3R,4S)-1-(N,N'-dibenzylamidino)-3,4,5,5-tetrahydroxy-2-hydroxymethylpiperidine hydrochloride
• CAS NO: 1010809-58-1
• Molecular Weight: 437.923
• Mol File: 1010809-58-1.mol

Chemical Properties

• CAS DataBase Reference: (2S,3R,4S)-1-(N,N'-dibenzylamidino)-3,4,5,5-tetrahydroxy-2-hydroxymethylpiperidine hydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,3R,4S)-1-(N,N'-dibenzylamidino)-3,4,5,5-tetrahydroxy-2-hydroxymethylpiperidine hydrochloride(1010809-58-1)
• EPA Substance Registry System: (2S,3R,4S)-1-(N,N'-dibenzylamidino)-3,4,5,5-tetrahydroxy-2-hydroxymethylpiperidine hydrochloride(1010809-58-1)

Safety Data

• Hazardous Substances Data: 1010809-58-1(Hazardous Substances Data)

Relevant articles and documents

Synthesis and biological evaluation of guanidine-type iminosugars

(Chemical Equation Presented) The preparation of carbohydrate mimics in which the endocyclic oxygen has been replaced by a guanidine-type nitrogen atom is reported. The synthetic strategy involves the furanose → piperidine rearrangement of 5-deoxy-5-guanidino-L-idose precursors. The reaction proceeds through elimination of water to give 3-oxopiperidines, which were isolated as the corresponding hydrates. Biological evaluation of the new glycomimetics evidenced a strong influence of the nature of the substituents at the nitrogen atoms on the glycosidase inhibitory properties.