17059-51-7

Basic information

• Product Name: 6-methylbenzofuran
• Synonyms: 6-methylbenzofuran;Einecs 241-122-6;6-methyl-1-benzofuran
• CAS NO: 17059-51-7
• Molecular Formula: C₉H₈O
• Molecular Weight: 132.15922
• EINECS: 241-122-6
• Mol File: 17059-51-7.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 191°Cat760mmHg
• Flash Point: 67.5°C
• Appearance: /
• Density: 1.077g/cm³
• Vapor Pressure: 0.729mmHg at 25°C
• Refractive Index: 1.587
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 6-methylbenzofuran(CAS DataBase Reference)
• NIST Chemistry Reference: 6-methylbenzofuran(17059-51-7)
• EPA Substance Registry System: 6-methylbenzofuran(17059-51-7)

Safety Data

• Hazardous Substances Data: 17059-51-7(Hazardous Substances Data)

Usage

General Description

6-methylbenzofuran, also known as 6-Me-BF, is a chemical compound with a molecular formula C9H8O. It is a naturally occurring aromatic compound found in various plant sources such as basil and saffron. It is also used in the synthesis of pharmaceuticals and perfumes due to its pleasant aroma. 6-methylbenzofuran has also been studied for its potential therapeutic properties, including its antioxidant and anti-inflammatory effects. Additionally, it is used as a flavoring agent in food and beverages. However, it is important to note that 6-methylbenzofuran may have potential health risks and should be handled with caution.

InChI:InChI=1/C9H8O/c1-7-2-3-8-4-5-10-9(8)6-7/h2-6H,1H3

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Relevant articles and documents

TRANSCRIPTION FACTOR BRN2 INHIBITORY COMPOUNDS AS THERAPEUTICS AND METHODS FOR THEIR USE

The invention provides a variety of compounds having the structure of Formula I and uses of such compounds for treatment of various indications, including cancer as well as methods of treatment involving such compounds are also provided. The uses of the compounds may specifically include: bladder cancer, cholangiocarcinoma; colorectal cancer; diffuse large B-cell lymphoma (DLBC); liver cancer; ovarian cancer; thymoma; thyroid cancer; clear cell renal cell carcinoma (CCRCC); chromophobe renal cell carcinoma (ChRCC); prostate cancer; breast cancer; uterine cancer; pancreatic cancer; cervical cancer; uveal melanoma; acute myeloid leukemia (AML); head and neck cancer; small cell lung cancer (SCLC); lung adenocarcinoma sarcoma; mesothelioma; adenoid cystic carcinoma (ACC), sarcoma; testicular germ cell cancer; uterine cancer; pheochromocytoma and paraganglioma (PCPG); melanoma; glioma; glioblastoma multiforme; T-cell Acute Lymphoblastic Leukemia; T-cell Lympohoma, medulloblastoma; and neuroblastoma.

OXADIAZINE COMPOUNDS AND METHODS OF USE THEREOF

The present disclosure relates to oxadiazine compounds, pharmaceutical compositions comprising an effective amount of an oxadiazine compound and methods for using an oxadiazine compound in the treatment of a neurodegenerative disease, comprising administering to a subject in need thereof an effective amount of an oxadiazine compound.

Zeolite-catalyzed synthesis of 2,3-unsubstituted benzo[b]furans via the intramolecular cyclization of 2-aryloxyacetaldehyde acetals

An efficient and environmentally benign heterogeneous catalytic process for the synthesis of 2,3-unsubstituted benzo[b]furans has been established via the intramolecular cyclization of 2-aryloxyacetaldehyde acetals. By utilizing tin-exchanged H-β zeolite (Sn-β) as catalyst, a wide range of functionalized 2,3-unsubstituted benzo[b]furans could be prepared in good to excellent yields. The Sn-β zeolite catalyst also exhibited excellent shape selectivity on the cyclization of meta-substituted 2-aryloxyacetaldehyde acetals, and 6-substituted isomers were preferably formed up to 97% regio-selectivity. Moreover, Sn-β zeolite could be easily recovered and reused without any noticeable activity loss.