2972-85-2 Usage
Description
[1-(4-methoxyphenyl)ethylidene]propanedinitrile, a chemical compound with the molecular formula C12H11N3O, is a nitrile derivative featuring a benzene ring with a methoxy group and a carboxylic acid group attached to an ethylidene chain. [1-(4-methoxyphenyl)ethylidene]propanedinitrile is recognized for its potential pharmacological activities and is often utilized in organic synthesis and pharmaceutical research.
Uses
Used in Pharmaceutical Research:
[1-(4-methoxyphenyl)ethylidene]propanedinitrile is used as a research compound for its potential antitumor properties, making it a valuable asset in cancer research. Its unique structure and pharmacological activities contribute to the development of novel therapeutic strategies against various types of cancer.
Used in Organic Synthesis:
As an intermediate, [1-(4-methoxyphenyl)ethylidene]propanedinitrile is employed in the synthesis of various other compounds, showcasing its versatility and importance in the field of organic chemistry. Its ability to be modified and incorporated into different molecular structures highlights its utility in creating new and potentially beneficial chemical entities.
Used in Chemical Intermediates Industry:
[1-(4-methoxyphenyl)ethylidene]propanedinitrile is used as a key intermediate in the production of various pharmaceuticals and other chemical products. Its role in this industry is crucial, as it enables the creation of a wide range of compounds with diverse applications, from medical treatments to industrial processes.
Check Digit Verification of cas no
The CAS Registry Mumber 2972-85-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,7 and 2 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2972-85:
(6*2)+(5*9)+(4*7)+(3*2)+(2*8)+(1*5)=112
112 % 10 = 2
So 2972-85-2 is a valid CAS Registry Number.
2972-85-2Relevant articles and documents
A [5 + 1] annulation strategy for the synthesis of multifunctional biaryls and: P -teraryls from 1,6-Michael acceptor ketene dithioacetals
Althagafi, Ismail,Elagamy, Amr,Kumar, Abhinav,Pratap, Ramendra,Shally,Shaw, Ranjay
, p. 6407 - 6417 (2020/09/07)
A new type of ketene dithioacetal, 2-(3,3-bis-methylsulfanyl-1-arylallylidene)malononitriles containing 1,4 and 1,6-Michael acceptors, were synthesized to study their reactivity for the synthesis of a new molecular entity. We report a [5 + 1] annulation s
"on Water" Direct Catalytic Vinylogous Aldol Reaction of Silyl Glyoxylates
Pan, Hong,Han, Man-Yi,Li, Pinhua,Wang, Lei
, p. 14281 - 14290 (2019/11/03)
The unique reactivity of water in the direct catalytic vinylogous aldol reaction of silyl glyoxylates is reported. With the hydrogen-bonding networks from water, the unfavorable homogeneous reactions in organic solvents were severely suppressed, and the "
Syntheses of donor-acceptor-functionalized dihydroazulenes
Broman, Soren Lindbaek,Jevric, Martyn,Bond, Andrew D.,Nielsen, Mogens Brondsted
, p. 41 - 64 (2014/01/17)
The dihydroazulene (DHA)/vinylheptafulvene (VHF) photo/thermoswitch has been of interest for use in molecular electronics and advanced materials. The switching between the two isomers has previously been found to depend strongly on the presence of donor a