224433-58-3

Basic information

• Product Name: (3R,4R,5R,6S)-3,4,5,6-tetra(benzyloxy)-cyclohexene
• Synonyms: (3R,4R,5R,6S)-3,4,5,6-tetra(benzyloxy)-cyclohexene
• CAS NO: 224433-58-3
• Molecular Weight: 506.642
• Mol File: 224433-58-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (3R,4R,5R,6S)-3,4,5,6-tetra(benzyloxy)-cyclohexene(CAS DataBase Reference)
• NIST Chemistry Reference: (3R,4R,5R,6S)-3,4,5,6-tetra(benzyloxy)-cyclohexene(224433-58-3)
• EPA Substance Registry System: (3R,4R,5R,6S)-3,4,5,6-tetra(benzyloxy)-cyclohexene(224433-58-3)

Safety Data

• Hazardous Substances Data: 224433-58-3(Hazardous Substances Data)

Upstream product

• 195873-65-5 (2S,3R,4S)-2,3,4-Tris-benzyloxy-hex-5-enal 
• 195873-64-4 3,4,5-tri-O-benzyl-1,2-dideoxy-D-xylohept-1-enitol 
• 195873-66-6 (3S,4R,5R)-tribenzyloxy-(6R)-hydroxyocta-1,7-diene 
• 18039-26-4 2,3,4-tri-O-benzyl-D-xylopyranose 
• 1023310-53-3 2,3,4,5-tetra-O-benzyl-1,6-di-O-trityl-D-glucitol 
• 29780-95-8 1,6-di-O-trityl-D-glucitol 
• 277744-72-6 1,6-di-O-[(4-methoxyphenyl)-diphenylmethyl]-2,3,4,5-tetra-O-benzyl-D-glucitol 
• 277744-69-1 1,6-di-O-[(4-methoxyphenyl)-diphenylmethyl]-D-glucitol 
• 256342-72-0 2,3,4,5-tetrakis-benzyloxyhexane-1,6-diol 
• 277744-76-0 2,3,4,5-tetra-O-benzyl-D-gluco-hexodialdose 
• 100-39-0 benzyl bromide 
• 50-70-4 D-sorbitol 
• 195873-70-2 (3R,4R,5R,6S)-3,4,5,6-tetra(benzoyloxy)-1,7-octadiene 
• 103066-43-9 (3S,4R,5R)-tribenzyloxy-(6R)-hydroxycyclohexene 

Downstream Products

• 13035-64-8 3,4,5,6-tetra-O-benzyl-L-chiro-inositol 

Relevant articles and documents

Enantio- and diastereodivergent synthetic route to multifarious cyclitols from D-xylose via ring-closing metathesis

Short stereoselective syntheses of various cyclitols, including the derivatives of conduritol B, conduritol F, myo-inositol, and chiro-inositol have been accomplished. The key steps in the syntheses are a ring-closing metathesis process and a diastereodiv

A straightforward synthesis of perbenzylated conduritols from alditols by ring closing olefin metathesis

The synthesis of perbenzylated conduritols A, E and F has been achieved in six steps by formal conversion of galactitol, D-mannitol and D-glucitol into the respective terminal dienes, followed by ring closing olefin metathesis. The Royal Society of Chemistry 1999.