58863-48-2

Basic information

• Product Name: BENZOFURAN, 3-BROMO-2-METHYL-
• Synonyms: BENZOFURAN, 3-BROMO-2-METHYL-;3-bromo-2-methylbenzofuran
• CAS NO: 58863-48-2
• Molecular Formula: C₉H₇BrO
• Molecular Weight: 211.06
• Mol File: 58863-48-2.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: BENZOFURAN, 3-BROMO-2-METHYL-(CAS DataBase Reference)
• NIST Chemistry Reference: BENZOFURAN, 3-BROMO-2-METHYL-(58863-48-2)
• EPA Substance Registry System: BENZOFURAN, 3-BROMO-2-METHYL-(58863-48-2)

Safety Data

• Hazardous Substances Data: 58863-48-2(Hazardous Substances Data)

Upstream product

• 4265-25-2 2-methylbenzofuran 
• 271-89-6 1-benzofurane 

Downstream Products

• 66022-00-2 1-hydroxy-2-(prop-1-ynyl)benzene 
• 1585983-48-7 1-(2-methyl-3-benzofuranyl)-2-(2-methylphenyl)perfluorocyclopentene 
• 1416881-64-5 (E)-N-(2-(2-methylbenzofuran-3-yl)ethyl)-3-(3,4,5-trimethoxyphenyl)acrylamide 
• 37797-72-1 2-(2-methylbenzofuran-3-yl)acetonitrile 
• 4265-25-2 2-methylbenzofuran 
• 1427283-27-9 1-(2-methyl-1-benzofuran-3-yl)-2-[2-methyl-5-(4-1,3-dioxolane-phenyl)-3-thienyl]perfluorocyclopentene 
• 1586038-80-3 1-(2-methyl-1-benzofuran-3-yl)-2-[2-methyl-5-(4-benzaldehyde)-3-thienyl]perfluorocyclopentene 
• 1364381-31-6 C₂₄H₁₅F₆NOS 
• 1364381-25-8 1-(2-methyl-3-benzofuryl)-2-(2-methyl-5-phenyl-3-thienyl)perfluorocyclopentene 
• 1345121-99-4 2,6-difluoro-N-(5-(2-methylbenzofuran-3-yl)pyrazin-2-yl)benzamide 
• 93782-20-8 -1-propyne 
• 3265-74-5 2-methyl-1-benzofuran-3-carboxylic acid 

Relevant articles and documents

Photochromic reaction behavior and thermal stability of thiophene-S,S-dioxidized diarylethenes having a benzofuryl group

Diarylethenes having a benzofuryl group and their thiophene-S,S-dioxidized diarylethenes were synthesized and their optical properties and thermal stability were investigated. Upon oxidation of the thiophene ring, the optical properties such as absorption

FUSED PYRIMIDINE COMPOUND, INTERMEDIATE, PREPARATION METHOD THEREFOR, AND COMPOSITION AND APPLICATION THEREOF

Disclosed are a fused pyrimidine compound, an intermediate, a preparation method therefor, and a composition and an application thereof. The present invention provides a fused pyrimidine compound shown in formula I, pharmaceutically acceptable salt, hydrate, solvate, and an optical isomer or prodrug of the compound. The present invention further provides applications of the fused pyrimidine compound shown in formula I, the pharmaceutically acceptable salt, the hydrate, solvate, and the optical isomer or the prodrug of the compound in the preparing drugs for curing and/or preventing a kinase-related disease. The fused pyrimidine compound I of the present invention is an efficient PI3 kinase depressor, and can be used to prepare drugs for preventing and/or curing cell-proliferation diseases such as cancer, infection, inflammation, and an autoimmune disease.

Regioselective copper-catalyzed chlorination and bromination of arenes with O2 as the oxidant

Electron-rich aromatic C-H bonds undergo regioselective chlorination and bromination in the presence of CuX2, LiX (X = Cl, Br) and molecular oxygen. Preliminary mechanistic insights suggest that the bromination and chlorination reactions proceed by different pathways.