123669-93-2

Basic information

• Product Name: 3,4-anhydro-1,2-dideoxy-4-methyl-D-threo-pentitol
• Synonyms: 3,4-anhydro-1,2-dideoxy-4-methyl-D-threo-pentitol
• CAS NO: 123669-93-2
• Molecular Weight: 116.16
• Mol File: 123669-93-2.mol
• Article Data: 17

Chemical Properties

• CAS DataBase Reference: 3,4-anhydro-1,2-dideoxy-4-methyl-D-threo-pentitol(CAS DataBase Reference)
• NIST Chemistry Reference: 3,4-anhydro-1,2-dideoxy-4-methyl-D-threo-pentitol(123669-93-2)
• EPA Substance Registry System: 3,4-anhydro-1,2-dideoxy-4-methyl-D-threo-pentitol(123669-93-2)

Safety Data

• Hazardous Substances Data: 123669-93-2(Hazardous Substances Data)

Upstream product

• 623-36-9 (E)-2-methylpent-2-enal 
• 16958-20-6 (Z)-2-methyl-2-penten-1-ol 
• 16958-19-3 (2E)-2-methyl-2-penten-1-ol 
• 1610-29-3 2-methyl-pent-2-en-1-ol 
• 546-68-9 titanium(IV) isopropylate 
• 405897-14-5 dimethyl tartrate 
• 225110-92-9 (+/-)-(2S^*,3S^*)-2,3-epoxy-2-methylpentan-1-ol 
• 1567-14-2 methyl (2E)-2-methyl-2-pentenoate 
• 1617-40-9 ethyl (E)-2-methyl-2-pentenoate 
• 182756-11-2 3,5-Dinitro-benzoic acid (2R,3R)-3-ethyl-2-methyl-oxiranylmethyl ester 

Downstream Products

• 123411-58-5 (2R,3R)-2-Methyl-1-phenylsulfanyl-pentane-2,3-diol 
• 72523-81-0 (+/-)-erythro-2,3-O-Isopropylidene-2,3-dihydroxy-2-methylpentanal 
• 408505-26-0 tert-butyl (2R,3S,5R)-5-cyano-2-{(1R,2S)-2-methoxy-2-methyl-1-[(tritylthio)amino]pentyl}-3-[(1Z)-prop-1-enyl]pyrrolidine-1-carboxylate 
• 408505-25-9 (2R,3S)-5-Methoxy-2-((1R,2S)-2-methoxy-2-methyl-1-tritylsulfanylamino-pentyl)-3-((Z)-propenyl)-pyrrolidine-1-carboxylic acid tert-butyl ester 
• 408505-23-7 tert-butyl (2R,3S)-2-{(1R,2S)-2-methoxy-2-methyl-1-[(triphenylmethylsulfenyl)amino]pentyl}-5-oxo-3-[(1Z)-prop-1-enyl]pyrrolidine-1-carboxylate 
• 408505-24-8 (2R,3S)-5-Hydroxy-2-((1R,2S)-2-methoxy-2-methyl-1-tritylsulfanylamino-pentyl)-3-((Z)-propenyl)-pyrrolidine-1-carboxylic acid tert-butyl ester 
• 335680-41-6 tert-butyl (2R)-2-{(1R,2S)-2-methoxy-1-[(4-methoxyphenyl)amino]-2-methylpentyl}-5-oxo-2,5-dihydro-1H-pyrrole-1-carboxylate 
• 335673-29-5 tert-butyl (2S)-2-{(1S,2S)-2-methoxy-1-[(4-methoxyphenyl)amino]-2-methylpentyl}-5-oxo-2,5-dihydro-1H-pyrrole-1-carboxylate 
• 471257-47-3 (1E,2S)-2-methoxy-2-methylpentanal S-tritylthioxime 
• 1026253-35-9 [(S)-2-Methoxy-2-methyl-pent-(E)-ylidene]-(4-methoxy-phenyl)-amine 
• 335637-15-5 ((((2S)-2-methoxy-2-methylpentyl)oxy)methyl)benzene 
• 335637-14-4 (2S)-1-(benzyloxy)-2-methyl-2-pentanol 
• 335679-69-1 A-315675 
• 335693-23-7 tert-butyl (2R)-2-{(1R,2S)-2-methoxy-2-methyl-1-[(triphenylmethylsulfenyl)amino]pentyl}-5-oxo-2,5-dihydro-1H-pyrrole-1-carboxylate 

Relevant articles and documents

Model studies for the synthesis of galbonolide B

The construction of the fourteen membered ring present in galbonolide B 1 is reported. The 10,11-diene system present in the southern portion of 1 has been constructed using an ester enolate rearrangement/silicon mediated fragmentation cascade, whilst the macrocycle has been synthesised following a Johnson rearrangement/mercury assisted ring closure protocol. The Royal Society of Chemistry 2005.

A formal stereoselective synthesis of (-)-maurenone

An efficient formal synthesis of marine polypropionate (-)-maurenone is described. Highlights of the strategy include the utilization of a desymmetrization technique and the activation of the epoxide oxygen with a silyl triflate followed by intramolecular hydride transfer - a novel transformation. Georg Thieme Verlag Stuttgart.

Five-membered carbocyclic and heterocyclic inhibitors of neuraminidases

Disclosed are compounds of the formula: which are useful for inhibiting neuraminidases from disease-causing microorganisms, especially, influenza neuraminidase. Also disclosed are compositions and methods for preventing and treating diseases caused by microorganisms having a neuraminidase, processes for preparing the compounds and synthetic intermediates used in these processes.