139399-64-7

Basic information

• Product Name: 6-broMoquinolin-8-ol
• Synonyms: 6-broMoquinolin-8-ol;8-Quinolinol, 6-broMo-;6-bromoquinolin-8-o
• CAS NO: 139399-64-7
• Molecular Formula: C₉H₆BrNO
• Molecular Weight: 224.05404
• Mol File: 139399-64-7.mol
• Article Data: 6

Chemical Properties

• Melting Point: 138-139 °C(Solv: water (7732-18-5); ethanol (64-17-5))
• Boiling Point: 363.2 °C at 760 mmHg
• Flash Point: 173.5 °C
• Appearance: /
• Density: 1.705 g/cm³
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: 4.25±0.30(Predicted)
• CAS DataBase Reference: 6-broMoquinolin-8-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 6-broMoquinolin-8-ol(139399-64-7)
• EPA Substance Registry System: 6-broMoquinolin-8-ol(139399-64-7)

Safety Data

• Hazardous Substances Data: 139399-64-7(Hazardous Substances Data)

Usage

Description

6-Bromoquinolin-8-ol is an organic compound with the molecular formula C9H6BrNO. It is a derivative of quinolinol, featuring a bromine atom at the 6th position and a hydroxyl group at the 8th position. 6-Bromoquinolin-8-ol is known for its potential applications in various industries, particularly as a chemical intermediate for the synthesis of fungicides.

Uses

Used in Agricultural Industry:
6-Bromoquinolin-8-ol is used as a chemical intermediate for the preparation of 3,6-dibromo-8-quinolinol fungicides. These fungicides exhibit fungicidal activity against a range of fungal pathogens, including Aspergillus niger, Aspergillus oryzae, Myrothecium verrucaria, Trichoderma viride, and Mucor cirinelloides. The compound plays a crucial role in protecting crops from these harmful fungi, thereby ensuring better crop yield and quality.

Upstream product

• 103028-32-6 6-bromo-8-methoxy-quinoline 
• 91715-77-4 2-Acetamido-5-bromophenyl Acetate 
• 57339-57-8 8-amino-6-bromoquinoline 
• 59557-91-4 4-bromo-2-methoxyaniline 
• 68527-67-3 6-bromo-8-nitroquinoline 
• 875-51-4 4-Bromo-2-nitroaniline 
• 88-74-4 2-nitro-aniline 
• 5467-64-1 2-acetamidophenyl acetate 

Downstream Products

• 834906-36-4 2,2-Dimethyl-propionic acid 6-{(S)-3-[bis-(4-methoxy-phenyl)-phenyl-methoxy]-2-hydroxy-propyl}-quinolin-8-yl ester 
• 834906-32-0 1-[bis-(4-methoxy-phenyl)-phenyl-methoxy]-3-[8-(tert-butyl-dimethyl-silanyloxy)-quinolin-6-yl]-propan-2-ol 
• 834906-34-2 6-[3-[bis-(4-methoxy-phenyl)-phenyl-methoxy]-2-(tert-butyl-dimethyl-silanyloxy)-propyl]-quinolin-8-ol 
• 834906-29-5 2,2-Dimethyl-propionic acid 6-{(2R,4S,5R)-5-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-hydroxy-tetrahydro-furan-2-yl}-quinolin-8-yl ester 
• 834906-35-3 2,2-dimethyl-propionic acid 6-[3-[bis-(4-methoxy-phenyl)-phenyl-methoxy]-2-(tert-butyl-dimethyl-silanyloxy)-propyl]-quinolin-8-yl ester 
• 834906-33-1 6-[3-[bis-(4-methoxy-phenyl)-phenyl-methoxy]-2-(tert-butyl-dimethyl-silanyloxy)-propyl]-8-(tert-butyl-dimethyl-silanyloxy)-quinoline 

Relevant articles and documents

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HISTONE DEMETHYLASE INHIBITORS FOR TREATING CANCERS

The present disclosure provides a new series of 8-hydroxyquinoline derivatives/analogs that are potent KDM4 inhibitors with high activity and selectivity against KDM4 enzymes. Also disclosed are the pharmaceutical compositions comprising such 8-hydroxyqui

An extremely stable and orthogonal DNA base pair with a simplified three-carbon backbone

A nucleotide C3HQ with a minimal three-carbon backbone displays unprecedented pairing strength and orthogonality in a homopair C3HQ:C3HQ in the presence of one equivalent of Cu2+. The pairing stability in DNA ev