93851-31-1

Basic information

• Product Name: Phenol, 3-(3-pyridinyl)-
• CAS NO: 93851-31-1
• Molecular Formula: C11H9NO
• Molecular Weight: 171.199
• Mol File: 93851-31-1.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: Phenol, 3-(3-pyridinyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Phenol, 3-(3-pyridinyl)-(93851-31-1)
• EPA Substance Registry System: Phenol, 3-(3-pyridinyl)-(93851-31-1)

Safety Data

• Hazardous Substances Data: 93851-31-1(Hazardous Substances Data)

Upstream product

• 591-20-8 3-Bromophenol 
• 89878-14-8 3-Diethylboranylpyridine 
• 626-55-1 3-Bromopyridine 
• 87199-18-6 3-hydroxyphenylboronic acid 
• 626-60-8 3-Chloropyridine 
• 10365-98-7 3-methoxyphenylboronic acid 
• 220565-63-9 pyridin-3-ylzinc(II) bromide 
• 626-02-8 3-Iodophenol 
• 1692-25-7 3-pyridylboronic acid 
• 4373-67-5 3-(3-methoxyphenyl)pyridine 

Downstream Products

• 870555-03-6 3-pyridin-3-yl-phenyl chloroformate 
• 702679-66-1 2-methyl-2-(3-pyridin-3-ylphenoxy)propionic acid ethyl ester 
• 1012886-72-4 C₁₂H₁₂NO⁽¹⁺⁾*I^(1-) 
• 1572184-62-3 (E)-N’-((1H-indol-4-yl)methylene)-2-(3-(pyridin-3-yl)phenoxy)acetohydrazide 
• 1572185-23-9 2-(3-(pyridin-3-yl)phenoxy)acetohydrazide 
• 194726-53-9 methyl 2-(3-(pyridin-3-yl)phenoxy)acetate 
• 1369788-02-2 2-methyl-2-(3-pyridin-3-ylphenoxy)propionic acid methyl ester 

Relevant articles and documents

COMPOUNDS AND METHODS FOR TREATING OXALATE-RELATED DISEASES

Disclosed herein are compounds and compositions for modulating glycolate oxidase, useful for treating oxalate-related diseases, such as hyperoxaluria, where modulating glycolate oxidase is expected to be therapeutic to a patent in need thereof. Methods of modulating glycolate oxidase activity in a human or animal subject is also provided.

Development of unimolecular tetrakis(piperidin-4-ol) as a ligand for Suzuki-Miyaura cross-coupling reactions: Synthesis of incrustoporin and preclamol

Abstract A domino aza-Cope/aza-Prins cascade enabled the synthesis of a new class of 4-hydroxypiperidine-appended mono, bis, tris, and tetrakis unimolecular compounds that served as efficient ligands to catalyze Suzuki-Miyaura cross-coupling reactions under aerobic conditions. Various biaryls, terphenyls, and heterocyclic biphenyls were obtained in good to excellent yields. The ligands were also capable of catalyzing the Heck-Mizoroki reaction. As an application, the Suzuki-Miyaura coupling reaction was used in the synthesis of incrustoporin, its analogs, and the drug molecule preclamol. A domino aza-Cope/aza-Prins cascade enabled the synthesis of a new class of 4-hydroxypiperidine-appended mono-, bis-, tris-, and tetrakis-unimolecular compounds that served as efficient ligands to catalyze Suzuki-Miyaura cross-coupling reactions under aerobic conditions. Various biaryls, terphenyls, and heterocyclic biphenyls were obtained in good to excellent yields.

2-Pyridyl and 3-pyridylzinc bromides: direct preparation and coupling reaction

A facile synthetic approach to the direct preparation of 2-pyridyl and 3-pyridylzinc bromides has been demonstrated using Rieke zinc with 2-bromopyridine and 3-bromopyridine, respectively. A variety of different electrophiles have been coupled with the resulting organozinc reagents to give the corresponding cross-coupling products in moderate to good yields.