40838-18-4

Basic information

• Product Name: .beta.-D-erythro-Hex-2-enopyranose, 1,6-anhydro-2,3-dideoxy-4-O-(phenylmethyl)-
• Synonyms: .beta.-D-erythro-Hex-2-enopyranose, 1,6-anhydro-2,3-dideoxy-4-O-(phenylmethyl)-
• CAS NO: 40838-18-4
• Molecular Formula: C₁₃H₁₄O₃
• Molecular Weight: 218.25
• Mol File: 40838-18-4.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 329.7±42.0 °C(Predicted)
• Appearance: /
• Density: 1.20±0.1 g/cm3(Predicted)
• CAS DataBase Reference: .beta.-D-erythro-Hex-2-enopyranose, 1,6-anhydro-2,3-dideoxy-4-O-(phenylmethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: .beta.-D-erythro-Hex-2-enopyranose, 1,6-anhydro-2,3-dideoxy-4-O-(phenylmethyl)-(40838-18-4)
• EPA Substance Registry System: .beta.-D-erythro-Hex-2-enopyranose, 1,6-anhydro-2,3-dideoxy-4-O-(phenylmethyl)-(40838-18-4)

Safety Data

• Hazardous Substances Data: 40838-18-4(Hazardous Substances Data)

Upstream product

• 112339-43-2 C₁₃H₁₆O₄ 
• 50705-28-7 1,6-anhydro-3,4-dideoxy-β-D-threo-hex-3-enopyranose 
• 100-51-6 benzyl alcohol 
• 134441-71-7 (2S,4R)-1-boc-4-tert-butyldimethylsilylpyrrolidine-2-carbaldehyde 
• 251085-95-7 Trifluoro-methanesulfonic acid (1R,2S,5R)-2-benzyloxy-6,8-dioxa-bicyclo[3.2.1]oct-3-en-4-yl ester 
• 161365-77-1 1,6-anhydro-2-chloro-β-D-erythro-hex-3-enopyranose 
• 58871-10-6 3,4-di-O-benzyl-D-glucal 
• 58394-31-3 1,6-anhydro-2,3-dideoxy-β-D-erythro-hex-2-enopyranose 
• 100-39-0 benzyl bromide 
• 33208-47-8 4-O-benzyl-1,6:2,3-dianhydro-β-D-mannopyranose 
• 2873-29-2 D-glucal triacetate 
• 13265-84-4 D-glucal 
• 102719-10-8 1,6-anhydro-4-O-benzyl-3-deoxy-β-D-erythro-hexopyranos-2-ulose 
• 37112-31-5 levoglucosenone 

Downstream Products

• 148473-54-5 Acetic acid (1R,2R,3S,4R,5R)-2-benzyloxy-4-bromo-6,8-dioxa-bicyclo[3.2.1]oct-3-yl ester 
• 26540-44-3 4-O-benzyl-1,6:2,3-dianhydro-β-D-allopyranoside 
• 33208-47-8 4-O-benzyl-1,6:2,3-dianhydro-β-D-mannopyranose 
• 110046-93-0 1,6-anhydro-4-O-benzyl-2-bromo-2-deoxy-β-D-glucopyranose 
• 20183-84-0 1,6-anhydro-4-O-benzyl-β-D-allopyranose 

Relevant articles and documents

Synthesis of α-bromoisolevoglucosenone and its cyclopenta annulation

4,4-Dimethyl-3-nitro-10,11-dioxatricyclo[6.2.1.02,6]undec-5-en-7-one possessing a bicyclic iridoid skeleton was synthesized in two steps from isolevoglucosenone which was obtained in turn from levoglucosenone through 4-benzyloxy-2-tosyloxy deri

Synthesis of 1,6-Anhydro-2-chloro-2,3,4-trideoxy-β-D-erythro-hex-3-enopyranose and its Stereospecific SN2' Substitution

The chlorination of 1,6-anhydro-3,4-dideoxy-β-D-threo-hex-3-enopyranose (2) with SOCl2 and pyridine gives predominantly 1,6-anhydro-2-chloro-β-D-erythro-hex-3-enopyranose (3).The chloride (3) takes place exclusively the suprafacial SN2' substit

Ein einfacher Weg von Glucal zu Cerny-Epoxiden

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