79324-77-9

Basic information

• Product Name: 3'-IODO-4'-METHOXYACETOPHENONE
• Synonyms: 3'-IODO-4'-METHOXYACETOPHENONE;3-IODO-4-METHOXYACETOPHENONE;1-(3-IODO-4-METHOXY-PHENYL)-ETHANONE;3'-Iodo-4'-methoxyacetophenone 97%;3'-Iodo-4'-methoxyacetophenone≥ 98% (GC)
• CAS NO: 79324-77-9
• Molecular Formula: C₉H₉IO₂
• Molecular Weight: 276.07
• Product Categories: Aromatic Acetophenones & Derivatives (substituted);C9;Carbonyl Compounds;Ketones;Building Blocks;Carbonyl Compounds;Chemical Synthesis;Organic Building Blocks
• Mol File: 79324-77-9.mol
• Article Data: 12

Chemical Properties

• Melting Point: 101-105 °C(lit.)
• Boiling Point: 340.1°C at 760 mmHg
• Flash Point: 159.5°C
• Appearance: /
• Density: 1.652g/cm³
• Vapor Pressure: 8.79E-05mmHg at 25°C
• Refractive Index: 1.583
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 3'-IODO-4'-METHOXYACETOPHENONE(CAS DataBase Reference)
• NIST Chemistry Reference: 3'-IODO-4'-METHOXYACETOPHENONE(79324-77-9)
• EPA Substance Registry System: 3'-IODO-4'-METHOXYACETOPHENONE(79324-77-9)

Safety Data

• Hazard Codes: Xn
• Statements: 22
• Safety Statements: 36
• RIDADR: UN 2811 6.1/PG 3
• WGK Germany: 3
• Hazardous Substances Data: 79324-77-9(Hazardous Substances Data)

Usage

Chemical Properties

Yellow powder

InChI:InChI=1/C9H9IO2/c1-6(11)7-3-4-9(12-2)8(10)5-7/h3-5H,1-2H3

Upstream product

• 6277-38-9 1-(4-methoxy-3-nitrophenyl)ethanone 
• 529-28-2 4-iodoanisol 
• 75-36-5 acetyl chloride 
• 6318-64-5 1-(3-amino-4-methoxyphenyl)ethan-1-one 
• 100-06-1 1-(4-methoxyphenyl)ethanone 

Downstream Products

• 1431944-46-5 3-acetyl-6-methoxy-2-methylbenzonitrile 
• 113016-89-0 5‐acetyl‐2‐methoxybenzonitrile 

Relevant articles and documents

Synthesis of 3-bromo-5-(2-ethylimidazo[1, 2-a]pyridine-3-carbonyl)-2-hydroxybenzonitrile

The invention discloses a synthetic method of 3-bromo-5-(2-ethylimidazo[1,2-a]pyridine-3-carbonyl)-2-hydroxybenzonitrile, particularly relates to a synthetic method of a compound shown as a formula (III), and particularly relates to a step A or a step B;

An investigation of structure‐activity relationships of azolylacryloyl derivatives yielded potent and long‐acting hemoglobin modulators for reversing erythrocyte sickling

Aromatic aldehydes that bind to sickle hemoglobin (HbS) to increase the protein oxygen affinity and/or directly inhibit HbS polymer formation to prevent the pathological hypoxia‐induced HbS polymerization and the subsequent erythrocyte sickling have for s

COMPOUND FOR TREATING OR PREVENTING HYPERURICEMIA OR GOUT

Provided are a compound as represented in formula (I), a pharmaceutically acceptable salts thereof, pharmaceutical compositions thereof, and uses thereof. The compound as represented in formula (I) and the pharmaceutically acceptable salts thereof are used in the preparation of medicines for the treatment or prevention of hyperuricemia or gout by means of uric acid excretion.