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

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

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 
• 1229291-78-4 2-iodo-4-methoxyphenyl acetate 
• 1356471-34-5 (E)-9-(2-hydroxy-5-methoxyphenyl)non-3-en-8-yn-2-one 
• 1356471-33-4 ethyl (E)-8-(2-hydroxy-5-methoxyphenyl)oct-2-en-7-ynoate 
• 1453187-98-8 butyl (E)-3-(5-methoxy-2-p-tolylbenzofuran-3-yl)acrylate 
• 122778-93-2 2-(2-Hydroxy-5-methoxyphenyl)-1-phenylethin 

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

Platinum-catalyzed α,β-unsaturated carbene formation in the formal syntheses of frondosin B and liphagal

Formal syntheses of tetracyclic terpenoids frondosin B and liphagal are described. Both synthetic routes rely on the use of platinum-catalyzed α,β-unsaturated carbene formation for the key C-C bond forming transformations. The successful route toward frondosin B utilizes a formal (4 + 3) cycloaddition, while the liphagal synthesis features the vinylogous addition of an enol nucleophile as a key step. Both synthetic routes are discussed, revealing insights into structural requirements in the catalytic a,β-unsaturated carbene reaction manifold.