19788-56-8

Basic information

• Product Name: α-(Benzoyloxy)-4-chlorobenzeneacetonitrile
• Synonyms: α-(Benzoyloxy)-4-chlorobenzeneacetonitrile
• CAS NO: 19788-56-8
• Molecular Formula: C₁₅H₁₀ClNO₂
• Molecular Weight: 271.6984
• Mol File: 19788-56-8.mol
• Article Data: 8

Chemical Properties

• Appearance: /
• CAS DataBase Reference: α-(Benzoyloxy)-4-chlorobenzeneacetonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: α-(Benzoyloxy)-4-chlorobenzeneacetonitrile(19788-56-8)
• EPA Substance Registry System: α-(Benzoyloxy)-4-chlorobenzeneacetonitrile(19788-56-8)

Safety Data

• Hazardous Substances Data: 19788-56-8(Hazardous Substances Data)

Usage

General Description

α-(Benzoyloxy)-4-chlorobenzeneacetonitrile is a chemical compound with the molecular formula C16H11ClN2O2. It is a white solid that is commonly used in organic synthesis and pharmaceutical research. α-(Benzoyloxy)-4-chlorobenzeneacetonitrile is a derivative of acetonitrile with a benzoyloxy and chlorobenzene group attached to the carbon atom. It is known to have various applications, including as an intermediate in the production of pharmaceutical drugs and as a reagent in organic chemistry reactions. α-(Benzoyloxy)-4-chlorobenzeneacetonitrile is considered to be a potentially hazardous compound and should be handled with care in a laboratory setting.

Upstream product

• 613-90-1 benzoyl cyanide 
• 104-88-1 4-chlorobenzaldehyde 
• 13014-48-7 4-chlorobenzoyl cyanide 
• 100-52-7 benzaldehyde 
• 116943-91-0 5-benzoyl-4,5-dihydro-6-methyl-1-phenyl-1H-pyrazolo<3,4-d>pyrimidine-4-carbonitrile 
• 151-50-8 potassium cyanide 
• 98-88-4 benzoyl chloride 

Downstream Products

• 99933-49-0 Benzoic acid (4-chloro-phenyl)-cyano-quinazolin-4-yl-methyl ester 
• 59563-90-5 (4-chloro-phenyl)-(1-phenyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)-methanone 
• 87412-79-1 1-phenyl-4-(p-chlorophenyl)pyrazolo<3,4-d>pyrimidine 
• 89549-81-5 Benzoic acid (4-chloro-phenyl)-cyano-(1-phenyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)-methyl ester 

Relevant articles and documents

Synthesis of Imidazoles and Oxazoles via a Palladium-Catalyzed Decarboxylative Addition/Cyclization Reaction Sequence of Aromatic Carboxylic Acids with Functionalized Aliphatic Nitriles

We herein report an efficient approach for the assembly of multiply substituted imidazoles and oxazoles in a single-step manner. These transformations are based on a decarboxylation addition and annulation of readily accessible aromatic carboxylic acids a

Divergent Palladium-Catalyzed Tandem Reaction of Cyanomethyl Benzoates with Arylboronic Acids: Synthesis of Oxazoles and Isocoumarins

A palladium-catalyzed tandem reaction of cyanomethyl benzoates with arylboronic acids has been achieved. Substitution at the 2-position of cyanomethyl benzoates was found to be crucial for the selective synthesis of oxazoles and isocoumarins. Cyanomethyl

A convenient and improved method for the preparation of cyanohydrin esters from acyl cyanides and aldehydes

Various kinds of cyanohydrin esters can be obtained in good to excellent yields from aldehydes by treatment with acyl cyanides in a heterogeneous mixture of aqueous potassium carbonate and acetonitrile.