1655-70-5

Upstream product

• 90-05-1 2-methoxy-phenol 
• 76652-99-8 3,5-dibromo-2-(3',5'-dibromo-2'-methoxyphenoxy)-1-methoxybenzene 
• 5720-06-9 2-Methoxyphenylboronic acid 
• 75-89-8 2,2,2-trifluoroethanol 
• 529-28-2 4-iodoanisol 
• 14064-94-9 2,2'-Dimethoxy-5-nitro-diphenylaether 
• 14064-89-2 2'-Methoxy-5-nitro-2-hydroxy-diphenylaether 
• 6437-46-3 1-(2-methoxyphenoxy)propan-2-one 
• 80246-27-1 2-(3',5'-dibromo-2'-hydroxyphenoxy)-3,4,5,6-tetrabromophenol 
• 14064-99-4 2,2'-Dimethoxy-5-amino-diphenylaether 
• 80246-28-2 2-(3',5'-dibromo-2'-methoxyphenoxy)-3,4,5,6-tetrabromoanisole 
• 80246-29-3 2-(3',5'-dibromo-2'-methoxyphenoxy)-3,5,6-tribromoanisole 
• 578-57-4 2-bromoanisole 

Downstream Products

• 100-66-3 methoxybenzene 
• 90-05-1 2-methoxy-phenol 
• 71-43-2 benzene 
• 1219927-05-5 3,3'-oxybis(2-hydroxybenzaldehyde) 
• 91-16-7 1,2-dimethoxybenzene 
• 931-56-6 2-methoxycyclohexane 
• 19752-95-5 1,2-dimethoxycyclohexane 
• 31708-14-2 1-cyclohexyl-1H-pyrrole 
• 4096-21-3 N-phenylpyrrolidine 

Relevant academic research and scientific papers

P2O5MsOH-mediated facile synthesis of semi-aromatic polyketones bearing 1,4-cyclohexanediyl units

Direct polycondensation of trans-1,4-cyclohexanedicarboxylic acid with several electron-rich arenes in a P2O5CH3SO3H (MsOH) mixture gave semi-aromatic polyketones bearing 1,4-cyclohexanediyl units in the main ch

Facile synthesis of trifluoroethyl aryl ethers through copper-catalyzed coupling of CF3CH2OH with aryl- and heteroaryl boronic acids

An efficient copper-catalyzed Chan-Lam reaction of trifluoroethanol with a variety of aryl- and heteroaryl boronic acids has been developed. This research provides a practical method to synthesize trifluoroethyl aryl ethers in moderate to good yields under mild conditions.

Synthesis of symmetrical diaryl ethers from arylboronic acids mediated by copper(II) acetate

Copper promoted generation of phenols in situ through arylation of water and their subsequent arylation with arylboronic acids affords a wide range of symmetrical diaryl ethers in good to high yield. The reaction is rapid, mild, convenient and tolerant of a wide range of functionalities on the arylboronic acid.

Macroring-Neutral Molecule Complexation. Synthesis of Biconcave Pyridino Hosts, Complex Formation, and X-ray Crystal Structures of Two Inclusion Compounds

A series of pyridino macrocycles 1-3(a-e) incorporating rigid bi- and triaryl ether segments in different ring positions have been synthesized.The effect of incorporation of these building blocks into a given macroring framework on the host properties for

POLYBROMINATED DIPHENYL ETHERS FROM DYSIDEA HERBACEA, DYSIDEA CHLOREA AND PHYLLOSPONGIA FOLIASCENS

The marine sponges Dysidea herbacea, D. chlorea and Phyllospongia foliascens were differentiated with difficulty in the field.D. herbacea contained 2-(2',4'-dibromophenoxy)-3,4,5-tribromophenol (1), 2-(2',4'-dibromophenoxy)-4,5,6-tribromophenol (2) and 2-(2',4'-dibromophenoxy)-3,5-dibromophenol (6).D. chlorea contained only 2-(2',4'-dibromophenoxy)-4.6-dibromophenol (3), a compound previously reported as a metabolite of D. herbacea.Phyllospongia foliascens contained 2-(3',5'-dibromo-2'-methoxy-phenoxy)-3,5-dibromoanisole (7) and a 1:2 mixture of 2-(3',5'-dibromo-2'-hydroxyphenoxy)-3,5,6-tribromophenol (8) and 2-(3',5'-dibromo-2'-hydroxy phenoxy)-3,4,5,6-tetrabromophenol (9).