100191-85-3 Usage
General Description
2-(4-Dimethylaminophenyl)furan is a chemical compound consisting of a furan ring with a 4-dimethylaminophenyl group attached in the 2 position. It is commonly used in the field of chemistry and pharmaceuticals for its unique properties. 2-(4-Dimethylaminophenyl)furan is known for its potential applications in organic synthesis, including its use as a building block for the creation of more complex chemical structures. Additionally, 2-(4-Dimethylaminophenyl)furan may also have potential biological activity, making it an area of interest for researchers in medicinal chemistry. Its structure and properties make it a valuable tool for the development of new chemicals and the study of chemical reactions.
Check Digit Verification of cas no
The CAS Registry Mumber 100191-85-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,1,9 and 1 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 100191-85:
(8*1)+(7*0)+(6*0)+(5*1)+(4*9)+(3*1)+(2*8)+(1*5)=73
73 % 10 = 3
So 100191-85-3 is a valid CAS Registry Number.
100191-85-3Relevant articles and documents
Impact of Five-membered Heterocyclic Rings on Photophysical Properties including Two-photon Absorption Character
Abe, Manabu,Chitose, Youhei,Lin, Tzu-Chau,Pham, Thuy Thi Thu,Tam, Tran Thi Thanh,Tseng, Wei-Lun
supporting information, p. 1810 - 1813 (2021/10/27)
A series of dipolar-type terphenyl derivatives 13 featuring an electron donor (p-NMe2C6H4 group) and acceptor (p-NO2C6H4 group) unit was synthesized and their photophysical properties were
Preparation of furans by palladium-catalyzed reaction of acylchromates and propargylic tosylates
Nakamura, Masaki,Yamane, Motoki,Sakurai, Hidehiro,Narasaka, Koichi
, p. 333 - 345 (2007/10/03)
Substituted furans are prepared by the palladium-catalyzed reaction of propargylic tosylates with acylchromates. The reaction is initiated by the oxidative additiion of propagylic tosylates to palladium(O) complexes to give 1,2-propadienylpalladium(II) co
