102719-10-8

Basic information

• Product Name: .beta.-D-erythro-Hexopyranos-2-ulose, 1,6-anhydro-3-deoxy-4-O-(phenylmethyl)-
• Synonyms: .beta.-D-erythro-Hexopyranos-2-ulose, 1,6-anhydro-3-deoxy-4-O-(phenylmethyl)-
• CAS NO: 102719-10-8
• Molecular Formula: C₁₃H₁₄O₄
• Molecular Weight: 234.25
• Mol File: 102719-10-8.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: .beta.-D-erythro-Hexopyranos-2-ulose, 1,6-anhydro-3-deoxy-4-O-(phenylmethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: .beta.-D-erythro-Hexopyranos-2-ulose, 1,6-anhydro-3-deoxy-4-O-(phenylmethyl)-(102719-10-8)
• EPA Substance Registry System: .beta.-D-erythro-Hexopyranos-2-ulose, 1,6-anhydro-3-deoxy-4-O-(phenylmethyl)-(102719-10-8)

Safety Data

• Hazardous Substances Data: 102719-10-8(Hazardous Substances Data)

Usage

General Description

".beta.-D-erythro-Hexopyranos-2-ulose, 1,6-anhydro-3-deoxy-4-O-(phenylmethyl)-" is a chemical compound with a complex molecular structure. It is a derivative of hexopyranos and contains an anhydro group and a phenylmethyl substituent. .beta.-D-erythro-Hexopyranos-2-ulose, 1,6-anhydro-3-deoxy-4-O-(phenylmethyl)- is a rare sugar with potential applications in pharmaceuticals, food additives, and other industries. Its unique structure and properties make it a valuable ingredient in various products and processes. Further research and development of this compound could lead to new advancements in the field of chemistry and related fields.

Upstream product

• 37112-31-5 levoglucosenone 
• 100-51-6 benzyl alcohol 

Downstream Products

• 112339-01-2 1,6-Anhydro-4-O-benzyl-3-deoxy-β-D-erythro-hexopyranos-2-ulose dimethyl acetal 
• 102719-12-0 2-O-acetyl-1,6-anhydro-4-O-benzyl-3-deoxy-β-D-arabino-hexopyranose 
• 102719-13-1 2-O-acetyl-1,6-anhydro-4-O-benzyl-3-deoxy-β-D-ribo-hexopyranose 
• 102719-14-2 2-O-acetyl-1,6-anhydro-3-deoxy-β-D-arabino-hexopyranose 
• 102719-15-3 2-O-acetyl-1,6-anhydro-3-deoxy-β-D-ribo-hexopyranose 
• 102719-16-4 Acetic acid (1R,4S,5R)-2-oxo-6,8-dioxa-bicyclo[3.2.1]oct-4-yl ester 
• 102719-16-4 Acetic acid (1R,4R,5R)-2-oxo-6,8-dioxa-bicyclo[3.2.1]oct-4-yl ester 
• 33647-85-7 isolevoglucosenone 
• 251085-97-9 (2S,4R)-2-[(R)-((1R,2S,3S,4S,5R)-2-Benzyloxy-3-hydroxy-6,8-dioxa-bicyclo[3.2.1]oct-4-yl)-hydroxy-methyl]-4-(tert-butyl-dimethyl-silanyloxy)-pyrrolidine-1-carboxylic acid tert-butyl ester 
• 251085-96-8 (2S,4R)-2-[(R)-((1R,2S,5R)-2-Benzyloxy-6,8-dioxa-bicyclo[3.2.1]oct-3-en-4-yl)-hydroxy-methyl]-4-(tert-butyl-dimethyl-silanyloxy)-pyrrolidine-1-carboxylic acid tert-butyl ester 
• 251086-00-7 (2S,4R)-2-[(R)-((2S,3R,4R,5S,6R)-5-Benzyloxy-4-hydroxy-6-hydroxymethyl-2-methoxy-tetrahydro-pyran-3-yl)-hydroxy-methyl]-4-hydroxy-pyrrolidine-1-carboxylic acid tert-butyl ester 
• 251085-99-1 (2S,4R)-2-[(R)-((2S,5S,6R)-5-Benzyloxy-6-hydroxymethyl-2-methoxy-5,6-dihydro-2H-pyran-3-yl)-hydroxy-methyl]-4-hydroxy-pyrrolidine-1-carboxylic acid tert-butyl ester 
• 40838-18-4 1,6-anhydro-4-O-benzyl-2,3-dideoxy-β-D-erythro-hex-2-enopyranose 
• 55639-83-3 1,6-anhydro-4-O-benzyl-3-deoxy-β-D-ribo-hexopyranose 

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

Factors Affecting Reaction of 1,6-Anhydrohexos-2-ulose Derivatives

1,6-Anhydrohexos-2-ulose derivatives undergo reaction with (trimethylsilyl)diazomethane in the presence of boron trifluoride etherate to afford structurally isomeric products.Ion-dipole interactions involving the 1,6-anhydro bridge and C4 substituents con