36758-77-7 Usage
Uses
Used in Organic Synthesis:
3-(DIMETHYLAMINO)-2-(4-METHOXYPHENYL)ACRYLONITRILE is used as a key building block for the production of various pharmaceuticals, agrochemicals, and materials, due to its unique chemical structure and reactivity.
Used in Fluorescence Spectroscopy and Imaging:
Leveraging its fluorescent properties, 3-(DIMETHYLAMINO)-2-(4-METHOXYPHENYL)ACRYLONITRILE is employed in the field of fluorescence spectroscopy and imaging, where its ability to emit light upon excitation can be utilized for analytical and diagnostic purposes.
Used in Photodynamic Therapy:
3-(DIMETHYLAMINO)-2-(4-METHOXYPHENYL)ACRYLONITRILE has potential application in photodynamic therapy, a cancer treatment modality that uses light-sensitive drugs to destroy cancer cells. Its fluorescent properties make it a candidate for the development of such light-sensitive drugs.
Used in Research and Development:
In the scientific community, 3-(DIMETHYLAMINO)-2-(4-METHOXYPHENYL)ACRYLONITRILE is used in research and development for exploring its chemical properties, potential applications, and effects on human health and the environment.
It is crucial to handle and use 3-(DIMETHYLAMINO)-2-(4-METHOXYPHENYL)ACRYLONITRILE with caution, as it may pose risks to human health and the environment. Proper safety measures and guidelines should be followed during its use in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 36758-77-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,7,5 and 8 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 36758-77:
(7*3)+(6*6)+(5*7)+(4*5)+(3*8)+(2*7)+(1*7)=157
157 % 10 = 7
So 36758-77-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H14N2O/c1-14(2)9-11(8-13)10-4-6-12(15-3)7-5-10/h4-7,9H,1-3H3/b11-9-
36758-77-7Relevant academic research and scientific papers
Application of vinylogous carbamates and vinylogous aminonitriles to the regiospecific synthesis of uniquely functionalized pyrroles and quinolones
Gupton, John T.,Crawford, Evan,Mahoney, Matt,Clark, Evan,Curry, Will,Lane, Annie,Shimozono, Alex,Moore-Stoll, Veronica,Elofson, Kristen,Juekun, Wen,Newton, Micah,Yeudall, Scott,Jaekle, Elizabeth,Kanters, Rene,Sikorski, James A.
, p. 7408 - 7420 (2018/11/23)
Pyrroles and quinolones represent core structures, which are routinely found in both natural and synthetic bioactive substances. Consequently, the development of efficient and regiospecific methods for the preparation of such heterocycles with unique functionality is of some importance. We describe herein the regiospecific synthesis of 1,2,3,4-tetrasubstituted pyrroles containing polar substituents and such products are prepared from vinylogous carbamates and vinylogous aminonitriles. We also describe the regiospecific synthesis of 3-aryl containing 1,3,6-trisubstituted quinolones from vinylogous carbamates. The use of an amine exchange reaction to prepare precursors for the pyrrole and quinolone forming cyclizations represents a key factor in the strategy.
An efficient, microwave assisted solvent-free synthesis of polarized enamines
Chanda, Kaushik,Dutta, Milan Ch.,Karim,Vishwakarma
, p. 791 - 793 (2007/10/03)
Reactions of acetophenones (1a-e), phenylacetonitriles (If-h) and nitromethane (1i) with dimethylformamide-dimethylacetal were carried out in domestic microwave oven to give 3-dimethylamino-1-arylprop-2-en-1-ones (2a-e), 3-dimethylamino-1-arylacrylonitril
