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

General Description

The chemical [(6Z)-6-(hydroxyimino)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl]methyl benzoate, also known by its non-preferred name, is a compound with a complex molecular structure. It consists of a tetrahydrofuran ring with a hydroxylamine group attached to it, as well as a benzene ring attached to a methyl benzoate group. This chemical may be used in various industrial and research applications, but its non-preferred name suggests that it is not commonly used or recognized by the scientific community. Its specific properties, potential uses, and safety considerations would need to be further evaluated and researched.

Upstream product

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

Downstream Products

• 102342-29-0 Benzoic acid (2S,3R,4R)-4-methanesulfonyloxy-5-methoxy-3-nitro-tetrahydro-furan-2-ylmethyl ester 
• 102419-25-0 Benzoic acid (S)-5-methoxy-3-nitro-2,5-dihydro-furan-2-ylmethyl ester 
• 102342-30-3 methyl 5-O-benzoyl-2,3-dideoxy-3-nitro-β-D-erythro-pentofuranoside 
• 102342-36-9 methyl 2,3-dideoxy-3-nitro-α-D-erythro-pentofuranosiduronic acid 
• 102342-35-8 methyl 2,3-dideoxy-3-nitro-β-D-erythro-pentofuranosiduronic acid 
• 93-58-3 benzoic acid methyl ester 
• 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 
• 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 
• 102342-31-4 Benzoic acid (2S,3R,4R,5R)-4-acetoxy-5-methoxy-3-nitro-tetrahydro-furan-2-ylmethyl ester 
• 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 
• 83905-12-8 O-benzoyl-5-desoxy-3-hydroxyamino-3-O-isopropylidene-1,2-α-D-ribofuranose 
• 91363-91-6 3-amino-5-O-benzoyl-3-deoxy-1,2-O-isopropylidene-α-D-ribofuranose 

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