METHYL 2,3-ANHYDRO-4,6-O-BENZYLIDENE-α-D-ALLOPYRANOSIDE

Names

[ Name ]:
METHYL 2,3-ANHYDRO-4,6-O-BENZYLIDENE-α-D-ALLOPYRANOSIDE

[Synonym ]:
MFCD00135407
Einecs 221-582-4
METHYL-2,3-ANHYDRO-4,6-O-BENZYLIDENE-A-D-ALLOPYRANOSIDE
methyl-2-3-anhydro-4-6-O-benzylidene*A-D-allopyra
METHYL-2-3-ANHYDRO-4-6-O-BENZYLIDENE*A-D-ALLOPYRANO
Methyl2,3-anhydro-4,6-O-benzylidene-a-D-allopyranose
(1aR,2S,3aR,7aR,7bR)-2-Methoxy-6-phenylhexahydrooxireno[2',3':4,5]pyrano[3,2-d][1,3]dioxine

Biological Activity

[Description]:

Methyl 2,3-anhydro-4,6-O-benzylidene-α-D-allopyranoside is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

[Related Catalog]:

Research Areas >> Others

Chemical & Physical Properties

[ Density]:
1.32g/cm3

[ Boiling Point ]:
391ºC at 760mmHg

[ Molecular Formula ]:
C₁₄H₁₆O₅

[ Molecular Weight ]:
264.27

[ Flash Point ]:
165.4ºC

[ Exact Mass ]:
264.10000

[ PSA ]:
49.45000

[ LogP ]:
1.23930

[ Index of Refraction ]:
1.577

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ RIDADR ]:
NONH for all modes of transport

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Articles

An alternative synthesis of methyl 2,3-anhydro-4,6-O-benzylidene-α-D-allopyranoside using carbonate esters Raaijmakers, H., et al.

Carbohydr. Res. 238 , 185-92, (1993)

Neighboring-group participation in benzylidene acetal ring-opening of a 2-cyano-2-deoxypyranoside derivative by diethylaluminum cyanide.

Carbohydr. Res. 338 , 2177-83, (2003)

The oxirane ring-opening of an anhydro sugar with diethylaluminum cyanide (Et(2)AlCN) is a direct approach for obtaining a cyano derivative. Methyl 2,3-anhydro-4,6-O-benzylidene-alpha-D-allopyranoside...

Reaction of methyl 2,3-anhydro-4,6-O-benzylidene-α-D-allopyranoside with ethanolamine and 1,4,7,10-tetraoxa-13-azacyclopentadecane Tóth, G., et al.

Carbohydr. Res. 168 , 141-5, (1987)

Related Compounds

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