566934-88-1

Basic information

• Product Name: 1,3-Dioxane-4-methanol, 2-phenyl-, (4R)-
• CAS NO: 566934-88-1
• Molecular Formula: C11H14O3
• Molecular Weight: 194.23
• Mol File: 566934-88-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1,3-Dioxane-4-methanol, 2-phenyl-, (4R)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Dioxane-4-methanol, 2-phenyl-, (4R)-(566934-88-1)
• EPA Substance Registry System: 1,3-Dioxane-4-methanol, 2-phenyl-, (4R)-(566934-88-1)

Safety Data

• Hazardous Substances Data: 566934-88-1(Hazardous Substances Data)

Usage

Physical state

Clear, colorless liquid

Odor

Floral

Usage

Production of pharmaceuticals and fragrances

Chirality

Chiral organic compound

Enantiomeric forms

Two enantiomeric forms exist, with (4R)-enantiomer being more commonly used and studied

Properties

Exhibits anti-inflammatory and analgesic properties

Application

Used as an intermediate in the synthesis of other pharmaceuticals and chemical compounds

Research and development

Subject of ongoing research in the field of medicinal chemistry due to potential therapeutic applications

Upstream product

• 1125-88-8 benzaldehyde dimethyl acetal 
• 70005-88-8 (R)-1,2,4-butanetriol 

Downstream Products

• 916428-55-2 (3R)-4-O-hexadecyl-1,3-O-benzylidine-1,3,4-butanetriol 
• 102794-93-4 [(E)-1-Benzenesulfonyl-2-((R)-2-phenyl-[1,3]dioxan-4-yl)-vinyl]-trimethyl-silane 
• 102794-93-4 [(Z)-1-Benzenesulfonyl-2-((R)-2-phenyl-[1,3]dioxan-4-yl)-vinyl]-trimethyl-silane 
• 102794-94-5 (R)-4-((S)-2-Benzenesulfonyl-1-methyl-ethyl)-2-phenyl-[1,3]dioxane 
• 102794-94-5 (R)-4-((R)-2-Benzenesulfonyl-1-methyl-ethyl)-2-phenyl-[1,3]dioxane 
• 566934-90-5 2,4-O-benzylidene-3-deoxy-L-glycero-tetronic acid 
• 102794-92-3 (4R)-2-phenyl-1,3-dioxane-4-carbaldehyde 
• 566934-72-3 5-methoxycarbonylpentyl 2-O-acetyl-3-O-benzyl-4-(2,4-O-benzylidene-3-deoxy-L-glycero-tetronamido)-4,6-dideoxy-α-D-mannopyranosyl-(1->2)-3-O-benzyl-4-(2,4-O-benzylidene-3-deoxy-L-glycero-tetronamido)-4,6-dideoxy-α-D-mannopyranoside 
• 566934-73-4 5-methoxycarbonylpentyl 3-O-benzyl-4-(2,4-O-benzylidene-3-deoxy-L-glycero-tetronamido)-4,6-dideoxy-α-D-mannopyranosyl-(1->2)-3-O-benzyl-4-(2,4-O-benzylidene-3-deoxy-L-glycero-tetronamido)-4,6-dideoxy-α-D-mannopyranoside 
• 566934-70-1 5-methoxycarbonylpentyl 2-O-acetyl-3-O-benzyl-4-(2,4-O-benzylidene-3-deoxy-L-glycero-tetronamido)-4,6-dideoxy-α-D-mannopyranoside 
• 566934-67-6 ethyl 2-O-acetyl-3-O-benzyl-4-(2,4-O-benzylidene-3-deoxy-L-glycero-tetronamido)-4,6-dideoxy-1-thio-α-D-mannopyranoside 

Relevant articles and documents

Synthetic studies toward marine toxic polyethers. 4. Synthesis of segment-A of okadaic acid via anti-selectivity by heteroconjugate addition

Segment-A of okadaic acid was synthesized in an optically active form by coupling the lithium acetylide (segment-A2) and the previously prepared segment-A1. The key step was the preparation of the anti-diastereoisomer for the C-12/13