56153-61-8

Basic information

• Product Name: o-Benzylbenzonitrile
• Synonyms: o-Benzylbenzonitrile;2-BENZYL BENZONITRILE
• CAS NO: 56153-61-8
• Molecular Formula: C₁₄H₁₁N
• Molecular Weight: 193.24384
• Mol File: 56153-61-8.mol
• Article Data: 29

Chemical Properties

• Appearance: /
• CAS DataBase Reference: o-Benzylbenzonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: o-Benzylbenzonitrile(56153-61-8)
• EPA Substance Registry System: o-Benzylbenzonitrile(56153-61-8)

Safety Data

• Hazardous Substances Data: 56153-61-8(Hazardous Substances Data)

Usage

Description

o-Benzylbenzonitrile, with the molecular formula C15H13N, is a colorless to light yellow liquid chemical compound. It is insoluble in water but soluble in organic solvents, and possesses a mild, almond-like odor.

Uses

Used in Pharmaceutical Industry:
o-Benzylbenzonitrile is used as a building block for the synthesis of pharmaceuticals, contributing to the development of new drugs and medicinal compounds.
Used in Dye Industry:
o-Benzylbenzonitrile is used as a building block for the synthesis of dyes, playing a role in the creation of various colorants for different applications.
Used in Fragrance Industry:
o-Benzylbenzonitrile is used as a fragrance ingredient, capitalizing on its mild, almond-like odor to enhance the scent profiles of various products.
Used in Material Science:
o-Benzylbenzonitrile is studied as a precursor to create new materials and polymers with unique properties, potentially leading to advances in material technology and innovation.

Upstream product

• 103606-45-7 3-(benzylimino)isobenzofuran-1-one 
• 140-29-4 phenylacetonitrile 
• 164594-13-2 Phenyl[2-(trimethylsilyl)phenyl]iodonium trifluoromethanesulfonate 
• 2042-37-7 o-cyanobromobenzene 
• 2549-31-7 4-methyl-2,5-diphenyloxazole 
• 92-71-7 2,5-diphenyloxazole 
• 591-50-4 iodobenzene 
• 6393-50-6 α-lithiophenylacetonitrile 
• 108-86-1 bromobenzene 
• 151-50-8 potassium cyanide 
• 29921-41-3 (o-benzyl)chlorobenzene 
• 529-19-1 2-Methylbenzonitrile 
• 7664-41-7 ammonia 
• 28493-54-1 benzyltributyltin 

Downstream Products

• 109845-54-7 (2-benzoylphenyl)(pyridin-2-yl)methanone 
• 390-30-7 2-benzyl-4'-fluoro-benzophenone 
• 102553-08-2 2-Benzylphenyl-cyclohexylketon 
• 185521-78-2 1-amino-3,4-dihydro-3-methyl-4-phenyl-2-naphthalenecarbonitrile 
• 13260-76-9 4-phenyl-1,4-dihydro-2H-benzo[d][1,3]oxazin-2-one 
• 6637-53-2 3-hydroxy-3-phenyl-2,3-dihydro-isoindol-1-one 
• 500311-00-2 C₁₈H₁₅NS 
• 1276042-01-3 (2-(2-naphthoyl)phenyl)(phenyl)methanone 
• 388-21-6 (2-benzoylphenyl)(4-fluorophenyl)methanone 
• 5778-02-9 (2-benzoylphenyl)(4-methylphenyl)methanone 
• 5778-00-7 (2-benzoylphenyl)(4-chlorophenyl)methanone 
• 5778-09-6 1-phenyl-4-p-tolylphthalazine 
• 6315-78-2 (2-benzoylphenyl)(2-methoxyphenyl)methanone 
• 1035-80-9 (2-benzoylphenyl)(thiophen-2-yl)methanone 

Relevant articles and documents

Nitrile Synthesis via Desulfonylative-Smiles Rearrangement

Herein, we designed a simple nitrile synthesis from N-[(2-nitrophenyl)sulfonyl]benzamides via base-promoted intramolecular nucleophilic aromatic substitution. The process features redox-neutral conditions as well as no requirement of toxic cyanide species and transition metals. Our process shows broad scope and various functional group compatibility, affording a variety of (hetero)aromatic nitriles in good to excellent yields.

Photo-Ni-Dual-Catalytic C(sp2)-C(sp3) Cross-Coupling Reactions with Mesoporous Graphitic Carbon Nitride as a Heterogeneous Organic Semiconductor Photocatalyst

The synergistic combination of a heterogeneous organic semiconductor mesoporous graphitic carbon nitride (mpg-CN) and a homogeneous nickel catalyst with visible-light irradiation at room temperature affords the C(sp2)-C(sp3) cross-co

Synthesis of bench-stable solid triorganoindium reagents and reactivity in palladium-catalyzed cross-coupling reactions

Bench-stable solid triorganoindium compounds have been prepared by coordination with 4-(dimethylamino)pyridine (DMAP). The solid R3In(DMAP) complexes are obtained from the corresponding solution of R3In in quantitative yield and can