436087-20-6 Usage
General Description
(1-Furan-2-yl-2-phenyl-ethyl)-(4-methoxy-phenyl)-amine is a chemical compound with the molecular formula C19H19NO, which consists of a furan ring attached to a phenylethyl group and a methoxy-phenyl group connected to an amine. (1-FURAN-2-YL-2-PHENYL-ETHYL)-(4-METHOXY-PHENYL)-AMINE is a derivative of aniline and has potential applications in the field of organic synthesis and pharmaceuticals. It possesses the characteristics of both furan and phenyl rings, which may contribute to its chemical and biological activities. Further research may be necessary to fully understand the properties and potential uses of this compound.
Check Digit Verification of cas no
The CAS Registry Mumber 436087-20-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,6,0,8 and 7 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 436087-20:
(8*4)+(7*3)+(6*6)+(5*0)+(4*8)+(3*7)+(2*2)+(1*0)=146
146 % 10 = 6
So 436087-20-6 is a valid CAS Registry Number.
InChI:InChI=1/C19H19NO2/c1-21-17-11-9-16(10-12-17)20-18(19-8-5-13-22-19)14-15-6-3-2-4-7-15/h2-13,18,20H,14H2,1H3
436087-20-6Relevant articles and documents
Alkyl transfer from C-C cleavage
Li, Guangxun,Chen, Rong,Wu, Lei,Fu, Qingquan,Zhang, Xiaomei,Tang, Zhuo
supporting information, p. 8432 - 8436 (2013/09/02)
Hydrogenation was only the beginning: Hantzsch esters have now been used to transfer alkyl groups to imines under mild catalytic conditions to provide a variety of amines (see scheme). Benzyl, secondary alkyl, and tertiary alkyl groups containing ether, ester, and hydroxy functionalities were transferred successfully. The use of Hantzsch esters as alkylation reagents offers a practical and complementary alternative to organometallic processes. Copyright
Regioselective domino metathesis of unsymmetrical 7-oxanorbornenes with electron-rich vinyl acetate toward biologically active glutamate analogues
Oikawa, Masato,Ikoma, Minoru,Sasaki, Makoto,Gill, Martin B.,Swanson, Geoffrey T.,Shimamoto, Keiko,Sakai, Ryuichi
experimental part, p. 5531 - 5548 (2010/02/28)
In this article a regioselective domino metathesis reaction of unsymmetrical 7-oxanorbornenes, readily available by a tandem Ugi/Diels-Alder reaction as a key step, promoted by the Hoveyda-Grubbs second-generation catalyst in the presence of electron-rich
