92287-20-2

Basic information

• Product Name: (5RS,6SR)-5-iodo-6-phenyltetrahydro-2H-pyran-2-one
• CAS NO: 92287-20-2
• Molecular Weight: 302.112
• Mol File: 92287-20-2.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: (5RS,6SR)-5-iodo-6-phenyltetrahydro-2H-pyran-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: (5RS,6SR)-5-iodo-6-phenyltetrahydro-2H-pyran-2-one(92287-20-2)
• EPA Substance Registry System: (5RS,6SR)-5-iodo-6-phenyltetrahydro-2H-pyran-2-one(92287-20-2)

Safety Data

• Hazardous Substances Data: 92287-20-2(Hazardous Substances Data)

Upstream product

• 119793-72-5 (E)-2-(3-phenyl-allyl) malonic acid dimethyl ester 
• 4392-24-9 Cinnamyl bromide 
• 4407-36-7 (2E)-3-phenyl-2-propen-1-ol 
• 4192-77-2 ethyl cinnamate 
• 100-52-7 benzaldehyde 
• 64-69-7 Iodoacetic acid 
• 4393-06-0 1-Phenyl-2-propen-1-ol 
• 28525-69-1 (4E)-5-phenyl-4-pentenoic acid 
• 17920-83-1 5-phenyl-4-pentenoic acid 

Downstream Products

• 17920-83-1 5-phenyl-4-pentenoic acid 

Relevant articles and documents

4-(Dimethylamino)pyridine-catalysed iodolactonisation of γ,δ-unsaturated carboxylic acids

4-(Dimethylamino)pyridine functioned as an excellent catalyst for iodolactonisation reactions of γ,δ-unsaturated carboxylic acids, affording γ-lactones, δ-lactones, or both under neutral conditions at room temperature. The effects of substrate structures

A Formal Intermolecular Iodolactonization Reaction Based on a Radical-Ionic Sequence

We report herein a method based on a radical-ionic sequence between an allylic alcohol and an α-iodo acid in the presence of substoichiometric amounts of lauroyl peroxide (DLP) to produce an atom transfer radical addition (ATRA) adduct, which subseqently

LEAD(IV) ACETATE-METAL HALIDE REAGENTS III. A NEW METHOD FOR THE SYNTHESIS OF TETRAHYDROFURAN, TETRAHYDROPYRAN AND LACTONE DERIVATIVES

A new method for the synthesis of tetrahydrofuran, tetrahydropyran and lactone derivatives from γδ-, δε-unsaturated alcohols and βγ-, γδ-carboxylic acids is described.