2-(Naphthalen-2-yl)acetonitrile

Name: 2-(Naphthalen-2-yl)acetonitrile | 7498-57-9
Brand: US-CATO
SKU: S57C3D-5951_10_MG
Price: 19998.0 USD
Availability: OutOfStock

Cat. No S57C3D-5951_10_MG

Vendor: US-CATO

Product Information

Product Name

2-(Naphthalen-2-yl)acetonitrile

Brand Name

US-CATO

Product Number

C3D-5951

CAS

7498-57-9

Certificate of Analysis (COA)

COA not found

General Information

PubChem CID

82008

IUPAC Name

2-naphthalen-2-ylacetonitrile

InChI Key

LPCWDVLDJVZIHA-UHFFFAOYSA-N

SMILES

C1=CC=C2C=C(C=CC2=C1)CC#N

References Data Source From Pubchem

Late-stage conversion of carboxylic acids to nitriles with Mg and Pd cocatalysis

Publication Name: Nature Catalysis

Publication Date: 2025-11-18

DOI: 10.1038/s41929-025-01446-y

Highly efficient and selective hydrogenation of α, β-unsaturated nitriles using supported palladium catalyst

Publication Name: Journal of the Iranian Chemical Society

Publication Date: 2024-02-27

DOI: 10.1007/s13738-023-02955-y

Oxidative Friedländer Reactions with (2-Aminopyridin-3-yl)methanol and Nitriles

Publication Name: Science of Synthesis

Publication Date: 2024

Oxidative Esterification of Arylacetonitriles and Related Compounds

Publication Name: Science of Synthesis

Publication Date: 2024

From sequence to function: a new workflow for nitrilase identification

Publication Name: Applied Microbiology and Biotechnology

Publication Date: 2020-04-14

DOI: 10.1007/s00253-020-10544-9

2-(Naphthalen-2-yl)acetonitrile

Product Information

General Information

References Data Source From Pubchem

Late-stage conversion of carboxylic acids to nitriles with Mg and Pd cocatalysis

Highly efficient and selective hydrogenation of α, β-unsaturated nitriles using supported palladium catalyst

Oxidative Friedländer Reactions with (2-Aminopyridin-3-yl)methanol and Nitriles

Oxidative Esterification of Arylacetonitriles and Related Compounds

From sequence to function: a new workflow for nitrilase identification