312534-71-7

Basic information

• Product Name: 4-Methoxy-2-iodophenol
• Synonyms: 4-Methoxy-2-iodophenol
• CAS NO: 312534-71-7
• Molecular Formula: C₇H₇IO₂
• Molecular Weight: 250.03375
• EINECS: -0
• Mol File: 312534-71-7.mol
• Article Data: 12

Chemical Properties

• Boiling Point: 258.1±20.0 °C(Predicted)
• Appearance: /
• Density: 1.866±0.06 g/cm3(Predicted)
• PKA: 9.00±0.18(Predicted)
• CAS DataBase Reference: 4-Methoxy-2-iodophenol(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Methoxy-2-iodophenol(312534-71-7)
• EPA Substance Registry System: 4-Methoxy-2-iodophenol(312534-71-7)

Safety Data

• Hazardous Substances Data: 312534-71-7(Hazardous Substances Data)

Upstream product

• 195314-47-7 2-bromo-4-methoxy-1-(methoxymethoxy)-benzene 
• 85630-18-8 N,N-diethyl-O-(4-methoxyphenyl)carbamate 
• 150-78-7 1,4-dimethoxybezene 
• 150-76-5 4-methoxy-phenol 

Downstream Products

• 333385-16-3 (R)-5-(5-Methoxy-benzofuran-2-yl)-hexanoic acid methyl ester 
• 333385-17-4 (-)-7-(2-hydroxy-5-methoxy-phenyl)-5-methyl-hept-6-ynoic acid methyl ester 
• 54888-83-4 2-(2-phenylethyl)-4-methoxyphenol 
• 1188366-04-2 C₁₇H₁₆O₄ 
• 1188366-11-1 C₁₇H₁₈O₄ 
• 26278-79-5 2-amino-6-hydroxybenzothiazole 
• 13391-27-0 5-methoxy-2-methylbenzofuran 
• 19803-11-3 6-methoxy-2-(4-methoxyphenyl)benzofuran 
• 52814-86-5 5-hydroxy-2-(4-hydroxyphenyl)benzo[b]furan 

Relevant articles and documents

BIARYL HYDROXYTHIOPHENE GROUP IV TRANSITION METAL POLYMERIZATION CATALYSTS WITH CHAIN TRANSFER CAPABILITY

Catalyst systems that include a chain transfer agent and a metal-ligand complex according to formula (I).

Benzofuran liquid crystal compound and composition thereof

The invention discloses a benzofuran liquid crystal compound containing a benzofuran ring. The structural general formula of the liquid crystal compound is (shown in the description), wherein R represents either one of the straight-chain paraffin with the

Synthesis of 8-azaprotosappanin A derivatives via intramolecular palladium-catalyzed ortho C-H activation/C-C cyclization and their antibacterial activity

A novel synthetic protocol for the construction of eight-membered heterocycles by intramolecular palladium-catalyzed ortho C-H activation/C-C cyclization was proposed. With protosappanin A as the lead compound, 25 derivatives of 8-azaprotosappanin A were prepared in good yields by this protocol. Besides, a plausible reaction mechanism of the intramolecular cyclization was proposed. This strategy could be widely used in the synthesis of some natural products and drugs with large heterocycles due to the fast reaction rate and the mild conditions. In vitro antimicrobial activities of the synthesized compounds were assessed against the strains of Gram-positive bacteria and linezolid and ciprofloxacin were selected as the standard drugs. Some of the synthesized compounds were found to have excellent antibacterial activities.