930590-05-9

Basic information

• Product Name: methyl (2E)-2-deoxy-2-[(dimethylamino)methylene]-4,6-O-[(R)-phenylmethylene]-α-D-erythro-hexopyranosid-3-ulose
• Synonyms: methyl (2E)-2-deoxy-2-[(dimethylamino)methylene]-4,6-O-[(R)-phenylmethylene]-α-D-erythro-hexopyranosid-3-ulose
• CAS NO: 930590-05-9
• Molecular Weight: 319.357
• Mol File: 930590-05-9.mol

Chemical Properties

• CAS DataBase Reference: methyl (2E)-2-deoxy-2-[(dimethylamino)methylene]-4,6-O-[(R)-phenylmethylene]-α-D-erythro-hexopyranosid-3-ulose(CAS DataBase Reference)
• NIST Chemistry Reference: methyl (2E)-2-deoxy-2-[(dimethylamino)methylene]-4,6-O-[(R)-phenylmethylene]-α-D-erythro-hexopyranosid-3-ulose(930590-05-9)
• EPA Substance Registry System: methyl (2E)-2-deoxy-2-[(dimethylamino)methylene]-4,6-O-[(R)-phenylmethylene]-α-D-erythro-hexopyranosid-3-ulose(930590-05-9)

Safety Data

• Hazardous Substances Data: 930590-05-9(Hazardous Substances Data)

Upstream product

• 63598-31-2 methyl 4,6-O-(R)-benzylidene-2-deoxy-α-D-erythrohexopyranosid-3-ulose 
• 4637-24-5 N,N-dimethyl-formamide dimethyl acetal 

Downstream Products

• 930590-06-0 (4S,5aR,8R,9aS)-2,5a,6,9a-tetrahydro-4-methoxy-2-methyl-8-phenyl-4H-[1,3]dioxino[4',5':5,6]pyrano[4,3-c]pyrazole 
• 1201090-82-5 2-(2,4-di-O-benzylidene-D-erytronoyl)pyrido[1,2-a]benzimidazole-4-carbonitrile 
• 1201090-78-9 ethyl 6-(2,4-di-O-benzylidene-D-erytronoyl)-2-methylsulfanyl-pyrazolo[1,5-a]pyrimidine-3-carboxylate 
• 1201090-80-3 2-(p-anisidino)-6-(2,4-di-O-benzylidene-D-erytronoyl)pyrazolo[1,5-a]pyrimidine-3-carbonitrile 
• 930590-09-3 (2R,4aR,6S,10bS)-4,4a,6,10b-tetrahydro-6-methoxy-9-methylsulfanyl-2-phenyl-[1,3]dioxino[4',5':5,6]-pyrano[4,3-d]-pyrimidine 
• 959921-64-3 (C₆H₅CH)C₆H₅O₃(OCH₃)CH₂N₂ 

Relevant articles and documents

Efficient functionalizations of a pyranosido-pyrimidine scaffold

Efficient reaction conditions have been developed to prepare highly functionalized chiral pyranosido-pyrimidine by regioselective alkylation of the pyranoside ring and palladium-catalyzed cross-coupling reaction on the pyrimidine ring under microwave acti

Synthesis of annelated pyranosides: a rapid and efficient entry to highly functionalized optically pure branched-pyrazoles

Pyrazolo-pyranosides prepared from methyl-2,3:4,6-di-O-benzylidene-α-d-mannopyranoside were functionalized to design new scaffolds suitable for peptidomimetic construction. Under certain acidic conditions, they undergo only pyranose ring-opening generatin

Nucleoside analogues from push-pull functionalized branched-chain pyranosides

The reaction of methyl 4,6-O-benzylidene-2-deoxy-α-D-erythro- hexopyranosid-3-ulose (1) with ethynylmagnesium bromide in tetrahydrofuran and subsequent trimethylsilylation yielded the methyl 4,6-O-benzylidene-2-deoxy-3-C- ethynyl-3-O-trimethylsilyl-α-D-ri