6974-51-2 Usage
Description
2-naphthalen-1-yl-2-phenyl-acetonitrile, also known as 2-(1-naphthyl)-2-phenylacetonitrile, is a chemical compound with the molecular formula C20H15N. It is a white solid in its pure form and is commonly used in organic synthesis and as a building block in the production of pharmaceuticals and agrochemicals. 2-naphthalen-1-yl-2-phenyl-acetonitrile features a naphthalene ring and a phenyl group connected to an acetonitrile functional group, making it a versatile intermediate in the synthesis of various organic compounds. Careful handling is advised due to potential hazards to human health and the environment.
Uses
Used in Organic Synthesis:
2-naphthalen-1-yl-2-phenyl-acetonitrile is used as a versatile intermediate in organic synthesis for the production of various organic compounds. Its unique structure with a naphthalene ring, phenyl group, and acetonitrile functional group allows for the creation of a wide range of chemical products.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 2-naphthalen-1-yl-2-phenyl-acetonitrile is used as a building block for the development of new drugs. Its structural features make it a valuable component in the synthesis of medicinal compounds with potential therapeutic applications.
Used in Agrochemical Production:
2-naphthalen-1-yl-2-phenyl-acetonitrile is also utilized in the agrochemical sector as a starting material for the synthesis of various agrochemicals. Its properties contribute to the development of effective products for agricultural use.
Check Digit Verification of cas no
The CAS Registry Mumber 6974-51-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,7 and 4 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6974-51:
(6*6)+(5*9)+(4*7)+(3*4)+(2*5)+(1*1)=132
132 % 10 = 2
So 6974-51-2 is a valid CAS Registry Number.
InChI:InChI=1/C18H13N/c19-13-18(15-7-2-1-3-8-15)17-12-6-10-14-9-4-5-11-16(14)17/h1-12,18H
6974-51-2Relevant articles and documents
Divergent synthesis of isonitriles and nitriles by palladium- catalyzed benzylic substitution with TMSCN
Hirano, Koji,Miura, Masahiro,Asai, Kento
, p. 12703 - 12714 (2020/11/09)
Ligand-controlled palladium-catalyzed divergent synthesis of isonitriles and nitriles from benzylic carbonates and TMSCN has been developed. The BINAP- or DPEphos-ligated palladium catalyst selectively provides the corresponding benzylic isonitriles, wher
Palladium-Catalyzed Regiodivergent Substitution of Propargylic Carbonates
Locascio, Theresa M.,Tunge, Jon A.
, p. 18140 - 18146 (2016/12/16)
The palladium(0)-catalyzed, ligand-controlled, regioselective addition of diaryl acetonitrile pronucleophiles to propargylic carbonates is reported. Selective formation of either terminal 1,3-dienyl or propargylated products is proposed to arise from a change in reaction mechanism controlled by the denticity of the coordinating ligand.
