88485-94-3 Usage
Description
(naphthalen-1-ylamino)(phenyl)acetonitrile, with the chemical formula C18H14N2, is a nitrile derivative featuring a naphthalene and phenyl group attached to the amino and nitrile functional groups, respectively. This chemical compound is known for its potential applications in chemical research and synthesis, as well as its interest in the pharmaceutical industry due to the diverse biological activities of nitrile-containing compounds. However, it is crucial to exercise proper handling and safety precautions when working with this compound due to its potential toxic or hazardous properties.
Uses
Used in Chemical Research and Synthesis:
(naphthalen-1-ylamino)(phenyl)acetonitrile is utilized as a building block in the creation of more complex molecules, contributing to the advancement of chemical research and synthesis. Its unique structure allows for the development of novel compounds with various applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (naphthalen-1-ylamino)(phenyl)acetonitrile is of interest due to the diverse biological activities associated with nitrile-containing compounds. Its potential use in drug development and design could lead to the creation of new therapeutic agents for various medical conditions.
Used in Application Industry:
(naphthalen-1-ylamino)(phenyl)acetonitrile is used as [application type] for [application reason]. (Please provide specific application type and reason for this industry if available.)
Check Digit Verification of cas no
The CAS Registry Mumber 88485-94-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,4,8 and 5 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 88485-94:
(7*8)+(6*8)+(5*4)+(4*8)+(3*5)+(2*9)+(1*4)=193
193 % 10 = 3
So 88485-94-3 is a valid CAS Registry Number.
88485-94-3Relevant articles and documents
A unique combination of KI/ZnFe2O4 as a catalyst for oxidative Strecker reaction
Ghandi, Leila,Kazemi Miraki, Maryam,Karimi, Meghdad,Radfar, Iman,Heydari, Akbar
, (2018/11/23)
α-Aminonitriles as key intermediates for the preparation of α-amino acid derivatives, amides, diamines, peptides, proteins and heterocycles were synthesized through methylarene oxidation in the Strecker reaction using a unique combination of KI/ZnFe2O4 as the best catalyst and aqueous tert-butyl hydroperoxide as oxidant. A wide range of amines and methylarenes were converted to the corresponding products. Operational simplicity, short reaction time and recyclability of the catalyst are advantages of this protocol.
One-pot three-component synthesis of α-aminonitriles using potassium hexacyanoferrate(II) as an eco-friendly cyanide source
Li, Zheng,Ma, Yuanhong,Xu, Jun,Shi, Jinghong,Cai, Hongfang
experimental part, p. 3922 - 3926 (2010/08/20)
An efficient and environmentally friendly method has been developed for the synthesis of α-aminonitriles via one-pot three-component condensation of carbonyl compounds, amines, and potassium hexacyanoferrate(II) in the presence of benzoyl chloride as a promoter. This protocol has the features of use of eco-friendly cyanide source, high yield, and simple work-up procedure.
Synthesis and pharmacological activities of arylarylamino- and aryl-aryliminoacetonitriles
Barnikow,Hagen,Hagen,Goeres,Richter,Fichtner
, p. 449 - 452 (2007/10/02)
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