62810-51-9

Basic information

• Product Name: 1-Pentanone, 1-(3-hydroxyphenyl)-
• CAS NO: 62810-51-9
• Molecular Formula: C11H14O2
• Molecular Weight: 178.231
• Mol File: 62810-51-9.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 1-Pentanone, 1-(3-hydroxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Pentanone, 1-(3-hydroxyphenyl)-(62810-51-9)
• EPA Substance Registry System: 1-Pentanone, 1-(3-hydroxyphenyl)-(62810-51-9)

Safety Data

• Hazardous Substances Data: 62810-51-9(Hazardous Substances Data)

Upstream product

• 5813-86-5 m-methoxybenzamide 
• 99-06-9 3-Carboxyphenol 
• 109-65-9 1-bromo-butane 
• 615558-48-0 3-hydroxy-N-methoxy-N-methylbenzamide 
• 2070921-87-6 C₉H₁₁BO₃ 
• 120-92-3 cyclopentanone 
• 152121-82-9 N,3‐dimethoxy‐N‐methylbenzamide 
• 586-38-9 3-Methoxybenzoic acid 
• 108-24-7 acetic anhydride 
• 109-72-8 n-butyllithium 
• 17264-90-3 m-methoxybenzoic acid Na-salt 
• 20359-55-1 1-(3-methoxyphenyl)pentan-1-one 

Downstream Products

• 20056-66-0 3-pentyl phenol 
• 1026152-43-1 N-(3-{3-[5-phenyl-2-(4-trifluoromethyl-phenyl)-oxazol-4-ylmethoxy]-phenyl}-hept-2-enyl)-hydroxylamine 
• 1027733-62-5 1-{3-[5-phenyl-2-(4-trifluoromethyl-phenyl)-oxazol-4-ylmethoxy]-phenyl}-pentan-1-one 
• 1025798-64-4 1-{3-[5-methyl-2-(4-trifluoromethyl-phenyl)-oxazol-4-ylmethoxy]-phenyl}-pentan-1-one 

Relevant articles and documents

Enantioselective synthesis of 3-substituted dihydrobenzofurans through iridium-catalyzed intramolecular hydroarylation

Intramolecular hydroarylationviaC-H activation is one of the most powerful methods to synthesize carbo- and heterocyclic compounds, whereas we still have room for developing a highly enantioselective variant of the reaction. Here we describe Ir-catalyzed enantioselective intramolecular hydroarylation ofm-allyloxyphenyl ketones. The enantioselective cyclization was efficiently catalyzed by a cationic iridium complex coordinated with a conventional chiral bisphosphine ligand to give benzofurans in high yields with high enantioselectivity. A carbonyl group of ketones functioned as an effective directing group for the C-H activation. In terms of synthetic utility, we also achieved one-pot synthesis of chiral 3-substituted dihydrobenzofurans from readily available allylic carbonates andm-hydroxyacetophenonesviasequential Pd-catalyzed allylic substitution and Ir-catalyzed intramolecular hydroarylation.

TETRAZOLINONE COMPOUND AND USE THEREOF

A tetrazolinone compound represented by formula (1): wherein R1 and R2 each represents a hydrogen atom, a halogen atom, or a C1-C3 alkyl group; R3 represents a C1-C3 alkyl group optionally having one or more halogen atoms; R4, R5, and R6 each represents a hydrogen atom or a halogen atom; R7 represents a C1-C3 alkyl group; Q represents a divalent group selected from Group P4; and A represents a C7-C18 aralkyloxy group optionally having one or more atoms or groups selected from Group P3, has excellent control activity against pests.

CHEMICAL COMPOUNDS

The present invention discloses novel compounds with a variety of therapeutic uses. More particularly, the invention discloses novel symmetrical triphenyl compounds that are particularly useful for selective estrogen receptor modulation.