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1222-61-3

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1222-61-3 Usage

General Description

The chemical (2Z)-3-[4-(dimethylamino)phenyl]-2-phenylprop-2-enenitrile, also known as DMAPN, is a compound with a molecular formula of C18H17N3. It is a yellow powder that is commonly used as a building block in organic synthesis and pharmaceutical research. DMAPN is known for its potential as a versatile intermediate in the synthesis of various biologically active compounds, including pharmaceuticals and agrochemicals. (2Z)-3-[4-(dimethylamino)phenyl]-2-phenylprop-2-enenitrile has been studied for its potential antiproliferative, anticancer, and anti-inflammatory activities, making it a valuable target for further research and development in the field of medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 1222-61-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,2 and 2 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1222-61:
(6*1)+(5*2)+(4*2)+(3*2)+(2*6)+(1*1)=43
43 % 10 = 3
So 1222-61-3 is a valid CAS Registry Number.

1222-61-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (Z)-3-[4-(dimethylamino)phenyl]-2-phenylprop-2-enenitrile

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:1222-61-3 SDS

1222-61-3Relevant articles and documents

Accelerated Discovery of α-Cyanodiarylethene Photoswitches

Hecht, Stefan,K?nig, Niklas F.,Mutruc, Dragos

supporting information, p. 9162 - 9168 (2021/07/01)

Cyanodiarylethene chromophores are able to undergo constitutional exchange via dynamic covalent chemistry (DCC). During this process, the central ethylene bridge of the molecular scaffold can be broken and thereby enables the assembly of a new combination of aryl moieties around the reformed ethylene bridge. The reversible CC double bond exchange has exemplarily been investigated using α-cyanostilbenes. Establishing a dynamic equilibrium reaction from α-cyanodiarylethene with arylacetonitriles under mild conditions has been the basis to access constitutional libraries of new photoswitches with potentially improved properties. When subject to irradiation with light of adequate wavelength, α-cyanodiarylethenes undergo Z/E isomerization followed by ring-closure. By screening the thus accessible dynamic chromophore libraries using a desired detection wavelength, we could identify specific dithienyl analogues that exhibit three-state photochromism. The combination of dynamic constitutional libraries of functional chromophores in combination with the light-guided screening and selection should lead to more rapid exploration of structural diversity dye chemistry.

α-Cyanostilbene based fluorophores: Aggregation-induced enhanced emission, solvatochromism and the pH effect

Palakollu, Veerabhadraiah,Kanvah, Sriram

, p. 5736 - 5746 (2015/02/19)

A series of α-cyanostilbenes substituted with dimethylaniline, diphenylaniline and carbazole was synthesized and their optical spectroscopic properties in homogeneous solvents, the dioxane-water binary mixture and the solid state were investigated. Stilbe

(Z)-2-(2-bromophenyl)-3-{[4-(1-methyl-piperazine)amino]phenyl}acrylonitrile (DG172): An orally bioavailable PPARβ/δ-selective ligand with inverse agonistic properties

Lieber, Sonja,Scheer, Frithjof,Meissner, Wolfgang,Naruhn, Simone,Adhikary, Till,Müller-Brüsselbach, Sabine,Diederich, Wibke E.,Müller, Rolf

supporting information; experimental part, p. 2858 - 2868 (2012/06/15)

The ligand-regulated nuclear receptor peroxisome proliferator-activated receptor β/δ (PPARβ/δ) is a potential pharmacological target due to its role in disease-related biological processes. We used TR-FRET-based competitive ligand binding and coregulator

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