29781-91-7

Basic information

• Product Name: [(6Z)-6-(hydroxyimino)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl]methyl benzoate (non-preferred name)
• CAS NO: 29781-91-7
• Molecular Formula: C₁₅H₁₇NO₆
• Molecular Weight: 307.2986
• Mol File: 29781-91-7.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 452.7°C at 760 mmHg
• Flash Point: 227.6°C
• Density: 1.41g/cm³
• Vapor Pressure: 5.54E-09mmHg at 25°C
• Refractive Index: 1.601
• CAS DataBase Reference: [(6Z)-6-(hydroxyimino)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl]methyl benzoate (non-preferred name)(CAS DataBase Reference)
• NIST Chemistry Reference: [(6Z)-6-(hydroxyimino)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl]methyl benzoate (non-preferred name)(29781-91-7)
• EPA Substance Registry System: [(6Z)-6-(hydroxyimino)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl]methyl benzoate (non-preferred name)(29781-91-7)

Safety Data

• Hazardous Substances Data: 29781-91-7(Hazardous Substances Data)

Usage

Description

[(6Z)-6-(hydroxyimino)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl]methyl benzoate (non-preferred name) is a complex organic compound featuring a tetrahydrofuran ring with a hydroxylamine group and a benzene ring connected to a methyl benzoate group. Its non-preferred name indicates that it may not be widely recognized or utilized within the scientific community, and further research would be necessary to determine its specific properties, potential applications, and safety considerations.

Uses

Used in Pharmaceutical Industry:
[(6Z)-6-(hydroxyimino)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl]methyl benzoate (non-preferred name) is used as a potential pharmaceutical compound for its possible biological activities, which may include therapeutic or medicinal applications. [(6Z)-6-(hydroxyimino)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl]methyl benzoate (non-preferred name)'s unique structure could offer novel interactions with biological targets, contributing to the development of new drugs or therapies.
Used in Chemical Research:
In the field of chemical research, [(6Z)-6-(hydroxyimino)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl]methyl benzoate (non-preferred name) may serve as a subject for studying reaction mechanisms, synthesis methods, and the exploration of new chemical properties. Its complex structure could provide insights into various chemical processes and potentially lead to the discovery of new synthetic pathways or applications.
Used in Material Science:
[(6Z)-6-(hydroxyimino)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl]methyl benzoate (non-preferred name) [(6Z)-6-(hydroxyimino)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl]methyl benzoate (non-preferred name) could be investigated for its potential use in material science, particularly in the development of new materials with unique properties. Its structural features might contribute to the creation of novel materials with specific characteristics, such as improved stability, reactivity, or selectivity in various applications.

Upstream product

• 6698-46-0 5-O-benzoyl-1,2-O-isopropylidene-α-D-ribofuranos-3-ulose 

Downstream Products

• 91363-91-6 3-amino-5-O-benzoyl-3-deoxy-1,2-O-isopropylidene-α-D-ribofuranose 
• 83905-12-8 O-benzoyl-5-desoxy-3-hydroxyamino-3-O-isopropylidene-1,2-α-D-ribofuranose 
• 34304-33-1 5-O-benzoyl-1,2-O-isopropylidene-3-deoxy-3-nitro-D-ribofuranose 
• 34304-34-2 5-O-benzoyl-1,2-O-isopropylidene-3-deoxy-3-nitro-D-xylofuranose 
• 102419-25-0 Benzoic acid (S)-5-methoxy-3-nitro-2,5-dihydro-furan-2-ylmethyl ester 
• 102342-31-4 Benzoic acid (2S,3R,4R,5R)-4-acetoxy-5-methoxy-3-nitro-tetrahydro-furan-2-ylmethyl ester 
• 102342-29-0 Benzoic acid (2S,3R,4R)-4-methanesulfonyloxy-5-methoxy-3-nitro-tetrahydro-furan-2-ylmethyl ester 
• 83905-37-7 N-((3aR,5S,6R,6aR)-2,2-Dimethyl-5-trityloxymethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-yl)-N-hydroxy-acetamide 
• 83905-36-6 N-Acetoxy-N-((3aR,5S,6R,6aR)-2,2-dimethyl-5-trityloxymethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-yl)-acetamide 
• 93-58-3 benzoic acid methyl ester 
• 102342-35-8 methyl 2,3-dideoxy-3-nitro-β-D-erythro-pentofuranosiduronic acid 
• 102342-36-9 methyl 2,3-dideoxy-3-nitro-α-D-erythro-pentofuranosiduronic acid 
• 102342-30-3 methyl 5-O-benzoyl-2,3-dideoxy-3-nitro-β-D-erythro-pentofuranoside 

Relevant articles and documents

Synthese d'acetals de desoxy-3-hydroxyamino-3-furannoses

Reduction of sugar ketoximes with NaBH3CN under acidic conditions constitutes a good synthetic pathway to deoxy(hydroxyamino)sugar derivatives.These compounds which are useful building blocks for the preparation of analogs of various classes of biological