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[4-(dibenzylamino)phenyl]acetonitrile, with the molecular formula C22H19N, is a nitrile derivative featuring a phenyl group substituted with a dibenzylamino group and a nitrile functional group attached to the phenyl ring. This chemical compound is recognized for its versatile reactivity, allowing it to undergo various chemical reactions to produce a range of compounds with potential biological activities.

211315-24-1

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211315-24-1 Usage

Uses

Used in Organic Synthesis:
[4-(dibenzylamino)phenyl]acetonitrile is utilized as a building block in organic synthesis, contributing to the creation of diverse chemical compounds.
Used in Pharmaceutical Development:
As a precursor for the synthesis of various pharmaceuticals, [4-(dibenzylamino)phenyl]acetonitrile plays a significant role in the development of new drugs, making it a valuable asset in the medicinal chemistry field.
Used in Agrochemical Synthesis:
[4-(dibenzylamino)phenyl]acetonitrile is also employed as a precursor in the synthesis of agrochemicals, further expanding its applications across different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 211315-24-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,1,3,1 and 5 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 211315-24:
(8*2)+(7*1)+(6*1)+(5*3)+(4*1)+(3*5)+(2*2)+(1*4)=71
71 % 10 = 1
So 211315-24-1 is a valid CAS Registry Number.

211315-24-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name [4-(Dibenzylamino)phenyl]acetonitrile

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:211315-24-1 SDS

211315-24-1Relevant academic research and scientific papers

N-2-(4-N-(4-[18F]Fluorobenzamido)phenyl)-propyl-2- propanesulphonamide: Synthesis and radiofluorination of a putative AMPA receptor ligand

Kronenberg, Ute B.,Drewes, Birte,Sihver, Wiebke,Coenen, Heinz H.

, p. 1169 - 1175 (2008/09/17)

Arylpropylsulphonamides are in the focus of research as α-amino-3-hydroxy-5-methyl-4-isoxazolpropionic acid (AMPA) receptor ligands. A new fluorine-18-labelled potentiator of AMPA receptors was synthesized as a potential radiotracer for cerebral imaging w

Sulphonamide derivatives

-

, (2008/06/13)

Glutamate receptor function in a mammal may be potentiated using an effective amount of a compound of formulaR1—L—NHSO2R2??Iin whichR1 represents an unsubstituted or substituted aromatic or heteroaromatic group;R2 represents (1-6C)alkyl, (3-6C)cycloalkyl, (1-6C)fluoroalkyl, (1-6C)chloroalkyl, (2-6C)alkenyl, (1-4C)alkoxy(1-4C)alkyl, phenyl which is unsubstituted or substituted by halogen, (1-4C)alkyl or (1-4C)alkoxy, or a group, of formula R3R4N in which R3 and R4 each independently represents (1-4C)alkyl or, together with the nitrogen atom to which they are attached form an azetidinyl, pyrrolidinyl, piperidinyl, morpholino, piperazinyl, hexahydroazepinyl or octahydroazocinyl group; andL represents a (2-4C)alkylene chain which is unsubstituted or substituted by one or two substituents selected independently from (1-6C)alkyl, aryl(1-6C)alkyl, (2-6C)alkenyl, aryl(2-6C)alkenyl and aryl, or by two substituents which, together with the carbon atom or carbon atoms to which they are attached form a (3-8C)carbocyclic ring;and pharmaceutically acceptable salts thereof.Also disclosed are compounds of formula I, processes for preparing them and pharmaceutical compositions containing them.

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