67205-87-2

Basic information

• Product Name: 4-CARBOETHOXY-4'-METHOXYBENZOPHENONE
• Synonyms: 4-CARBOETHOXY-4'-METHOXYBENZOPHENONE
• CAS NO: 67205-87-2
• Molecular Formula: C₁₇H₁₆O₄
• Molecular Weight: 284.31
• Mol File: 67205-87-2.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 435.4°C at 760 mmHg
• Flash Point: 193°C
• Appearance: /
• Density: 1.155g/cm³
• Vapor Pressure: 8.76E-08mmHg at 25°C
• Refractive Index: 1.556
• CAS DataBase Reference: 4-CARBOETHOXY-4'-METHOXYBENZOPHENONE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-CARBOETHOXY-4'-METHOXYBENZOPHENONE(67205-87-2)
• EPA Substance Registry System: 4-CARBOETHOXY-4'-METHOXYBENZOPHENONE(67205-87-2)

Safety Data

• Hazardous Substances Data: 67205-87-2(Hazardous Substances Data)

Usage

InChI:InChI=1/C17H16O4/c1-3-21-17(19)14-6-4-12(5-7-14)16(18)13-8-10-15(20-2)11-9-13/h4-11H,3H2,1-2H3

Upstream product

• 64-17-5 ethanol 
• 27645-60-9 4-(4-methoxybenzoyl)benzonitrile 
• 13139-86-1 4-methoxyphenyl magnesium bromide 
• 727409-13-4 4-ethoxycarbonylbenzoyl cyanide 
• 713-57-5 terephthalic acid monoethyl ester 
• 27111-45-1 ethyl 4-(chlorocarbonyl)benzoate 
• 51934-41-9 4-iodobenzoic acid ethyl ester 
• 123-11-5 4-methoxy-benzaldehyde 
• 54118-75-1 4-bromo-4'-methoxybenzophenone 
• 100-07-2 4-methoxy-benzoyl chloride 
• 104-92-7 1-bromo-4-methoxy-benzene 

Downstream Products

• 67205-88-3 ethyl 4-(4-methoxybenzyl) benzoate 
• 679390-88-6 4-[1-(4-methoxy-phenyl)-vinyl]-benzoic acid ethyl ester 
• 67205-85-0 4-[4-(4-hydroxybenzyl)benzyl]heptane-3,5-dione 
• 67205-84-9 4-[4-(4-methoxybenzyl)benzyl]heptane-3,5-dione 
• 67205-89-4 4-(4-methoxybenzyl)benzoic acid 

Relevant articles and documents

Magnesium salt promoted tandem nucleophilic addition-Oppenauer oxidation of aldehydes with organozinc reagents

A magnesium salt promoted synthesis of ketones via tandem nucleophilic addition-Oppenauer oxidation of aldehydes using organozinc chemistry was demonstrated. Magnesium salts concomitantly generated via magnesium metal mediated organohalide zincation exhibit high efficacy for nucleophilic addition of organozinc reagents to aromatic aldehydes and thereafter Oppenauer oxidation whereby ketones are formed in high to excellent yields.

Unmasked acyl anion equivalent from acid chloride with indium: Reversed-polarity synthesis of unsymmetric aryl aryl and alkenyl aryl ketone through palladium-catalyzed cross-coupling reaction

A reversed-polarity synthetic method of a range of unsymmetric aryl aryl and alkenyl aryl ketones has been developed through Pd-catalyzed cross-coupling reaction of acylindium reagents generated in situ from easily available acid chlorides and indium with various electrophiles such as aryl iodide and triflate and alkenyl triflate.

The crocacins: Novel natural products as leads for agricultural fungicides

A short route to the synthesis of analogues of the antifungal but unstable natural product crocacin D was developed. A wide range of compounds were made in which the complex side chain was replaced by simple aromatic units, and many of them showed high activity in a mitochondrial beef heart respiration assay. Some of these compounds were active against plant pathogenic fungi of agricultural importance in glasshouse tests. In order to find compounds with greater stability than the natural crocacins, the photolabile (Z)-enamide was replaced with many different moieties, but none gave rise to useful fungicidal activity.