99948-46-6

Basic information

• Product Name: 2H-Pyran, tetrahydro-2-[(2-iodophenyl)methoxy]-
• CAS NO: 99948-46-6
• Molecular Formula: C12H15IO2
• Molecular Weight: 318.154
• Mol File: 99948-46-6.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: 2H-Pyran, tetrahydro-2-[(2-iodophenyl)methoxy]-(CAS DataBase Reference)
• NIST Chemistry Reference: 2H-Pyran, tetrahydro-2-[(2-iodophenyl)methoxy]-(99948-46-6)
• EPA Substance Registry System: 2H-Pyran, tetrahydro-2-[(2-iodophenyl)methoxy]-(99948-46-6)

Safety Data

• Hazardous Substances Data: 99948-46-6(Hazardous Substances Data)

Upstream product

• 110-87-2 3,4-dihydro-2H-pyran 
• 5159-41-1 2-iodobenzyl alcohol 
• 88-67-5 2-Iodobenzoic acid 

Downstream Products

• 1196708-17-4 C₁₆H₂₂O₂ 
• 121089-46-1 (2-(but-3-en-1-yl)phenyl)methanol 
• 54193-74-7 4-methyl-3-phenyl-1H-isochromene 
• 5159-41-1 2-iodobenzyl alcohol 
• 1170658-90-8 C₁₈H₂₄O₃ 
• 1170658-85-1 C₁₇H₂₂O₃ 
• 220316-66-5 2-tetrahydropyranyloxymethyl-1-(3-phenylsulfonylpropynyl)benzene 
• 220316-65-4 2-tetrahydropyranyloxymethyl-1-(3-phenylthiopropynyl)benzene 
• 221534-34-5 2-(2-Ethynyl-benzyloxy)-tetrahydro-pyran 
• 328394-71-4 C₁₇H₂₂O₃ 
• 220316-64-3 2-tetrahydropyranyloxymethyl-1-(3-hydroxypropynyl)benzene 
• 99948-47-7 2-(((tetrahydro-2H-pyran-2-yl)oxy)methyl)benzaldehyde 

Relevant articles and documents

Transition-Metal-Free α-Arylation of Enolizable Aryl Ketones and Mechanistic Evidence for a Radical Process

The α-arylation of enolizable aryl ketones can be carried out with aryl halides under transition-metal-free conditions using KOtBu in DMF. The α-aryl ketones thus obtained can be used for step- and cost-economic syntheses of fused heterocycles and Tamoxifen. Mechanistic studies demonstrate the synergetic role of base and solvent for the initiation of the radical process.

Simple and efficient method for tetrahydropyranylation of alcohols and phenols by using silica supported sodium hydrogen sulphate as a catalyst

A Simple and efficient process for tetrahydropyranylation of alcohols and phenols has been developed by reacting with dihydropyran at room temperature in presence of catalytic amount of silica supported sodium hydrogen sulphate.

Aza Hopf cyclization: synthesis and reactivity of cyclic azadieneynes

Nine- and 10-membered azadieneynes have been synthesized for the first time via an intramolecular aza Wittig reaction. The compounds undergo Hopf cyclization under ambient conditions to the hydroxy dihydroisoquinoline derivatives.