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

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

• 108-24-7 acetic anhydride 
• 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 
• 5813-86-5 m-methoxybenzamide 
• 109-72-8 n-butyllithium 
• 17264-90-3 m-methoxybenzoic acid Na-salt 
• 20359-55-1 1-(3-methoxyphenyl)pentan-1-one 

Downstream Products

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

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.

Suzuki-Miyaura coupling of simple ketones via activation of unstrained carbon-carbon bonds

Here, we describe that simple ketones can be efficiently employed as electrophiles in Suzuki-Miyaura coupling reactions via catalytic activation of unstrained C-C bonds. A range of common ketones, such as cyclopentanones, acetophenones, acetone and 1-indanones, could be directly coupled with various arylboronates in high site-selectivity, which offers a distinct entry to more functionalized aromatic ketones. Preliminary mechanistic study suggests that the ketone α-C-C bond was cleaved via oxidative addition.

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.

CHEMICAL COMPOUNDS

The present invention discloses to 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.

Preparation of m-acylphenol derivatives by the reaction of tricarbonyl(cyclohexadienone)iron complex and higher order cuprates

Reaction of tricarbonyl[(2,3,4,5-η)-2,4-cyclohexadien-1-one]iron and higher order cuprates followed by the treatment with acetic anhydride and then with carbon monoxide affords tricarbonyl[(1,2,3,4-η)-1-acetoxy-5-endo-acyl-1,3-cyclohexadiene]iron complexe