606930-14-7

Basic information

• Product Name: (2S,3R,4S)-2,3,4-tris-benzyloxy-5-hydroxycyclohexan-1-one
• Synonyms: (2S,3R,4S)-2,3,4-tris-benzyloxy-5-hydroxycyclohexan-1-one
• CAS NO: 606930-14-7
• Molecular Weight: 432.516
• Mol File: 606930-14-7.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: (2S,3R,4S)-2,3,4-tris-benzyloxy-5-hydroxycyclohexan-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,3R,4S)-2,3,4-tris-benzyloxy-5-hydroxycyclohexan-1-one(606930-14-7)
• EPA Substance Registry System: (2S,3R,4S)-2,3,4-tris-benzyloxy-5-hydroxycyclohexan-1-one(606930-14-7)

Safety Data

• Hazardous Substances Data: 606930-14-7(Hazardous Substances Data)

Upstream product

• 97321-72-7 methyl 2,3,4-tri-O-benzyl-6-deoxy-6-phenylseleno-α-D-glucopyranoside 
• 53008-65-4 methyl 2,3,4-tri-O-benzyl-D-glucopyranoside 
• 4144-87-0 methyl 6-chloro-6-deoxy-α-D-glucopyranoside 
• 97-30-3 methyl-alpha-D-glucopyranoside 
• 6304-96-7 methyl 2,3,4-tri-O-acetyl-6-deoxy-6-iodo-α-D-glucopyranoside 
• 6217-21-6 methyl 2,3,4-tri-O-acetyl-6-desoxy-α-D-xylo-hex-5-enopyranoside 
• 100-39-0 benzyl bromide 
• 85716-44-5 methyl 2,3,4-tri-O-benzyl-α-d-xylo-hex-5-enopyranoside 
• 13265-83-3 methyl 6-deoxy-α-D-xylo-hex-5-enopyranoside 

Downstream Products

• 110372-60-6 2D-(2,4/3)-2,3,4-Tri-O-benzyl-5,5-bis-C-(ethylthio)-2,3,4-trihydroxy-1-cyclohexanon 
• 110372-61-7 2,3,4-Tri-O-benzyl-5,5-bis-C-(ethylthio)-1-O-(ethylthio)methyl-1,2,3,4-cyclohexantetrol 
• 110372-62-8 Acetic acid (2S,3R,4S)-2,3,4-tris-benzyloxy-5,5-bis-ethylsulfanyl-cyclohexyl ester 
• 107960-16-7 Acetic acid (1S,2S,3R,4S,5S)-2,3,4-tris-benzyloxy-5-cyano-5-ethylsulfanyl-cyclohexyl ester 
• 107960-16-7 Acetic acid (1R,2S,3R,4S,5S)-2,3,4-tris-benzyloxy-5-cyano-5-ethylsulfanyl-cyclohexyl ester 
• 131289-28-6 (2S,3R,4R,5S) 5-<(t-butyldimethylsilyl)oxy>-2,3,4-tris(benzyloxy) cyclohexane-1-one 
• 159701-13-0 (2S,3R,4R,5R) 5-<(t-butyldimethylsilyl)oxy>-2,3,4-tris(benzyloxy) cyclohexane-1-one 
• 528815-13-6 3-deoxy-2-C-ethenyl-1,5,6-tris-O-(phenylmethyl)-D-myo-inositol 
• 131289-23-1 (1S)-(1O,2,4,5/1C,3)-2,3,4-tribenzyloxy-1-vinylcyclohexane-1,5-diol 
• 107960-21-4 Benzoic acid (3S,4S,5S,6R)-4,5,6-tris-benzyloxy-3-(toluene-4-sulfonylamino)-cyclohex-1-enylmethyl ester 
• 107960-19-0 Benzoic acid (1S,2S,3R,4S)-2,3,4-tris-benzyloxy-1-ethylsulfanyl-5-hydroxy-cyclohexylmethyl ester 
• 107960-16-7 1L-(1S,2,4/1C,3)-5-O-Acetyl-2,3,4-tri-O-benzyl-1-C-(ethylthio)-2,3,4,5-tetrahydroxy-1-cyclohexancarbonitril 
• 38231-86-6 valienamine 
• 151557-55-0 ((1R,2S,3R,4R,5S,6S)-2,3,4-Tris-benzyloxy-5,6-dihydroxy-cyclohexyl)-acetic acid ethyl ester 

Relevant articles and documents

Do upper limits to the multiple spiro acetalization of the cyclohexane ring exist?

An attempt to transform the pyranoside (5) into the bifaciai ligand (3) is described. The first subtarget is acetal (13) whose conversion into tris acetal (17) is made possible by remote C-H activation. Regrettably, triol (20) does not lend itself to comparable triple cyclization.

β-acarbose. I. The synthesis of 1-epivalienamine

Improvements and modifications to a literature procedure for the synthesis of multigram amounts of a derivative of 1-epivalienamine are described. As well, various other derivatives of 1-epivalienamine, of potential use in the synthesis of carba sugars, a

Synthesis of new aminocyclitols as potent enzymatic inhibitors

The syntheses of new pseudo-saccharides having an allylic amino moiety or an aziridine group are reported starting from methyl-α-D-glucopyranoside. To enhance the hydrophilic/lipophilic balance, pseudo-saccharides 9 and 10 were linked with a glycosyl deri