13924-50-0 Usage
Description
BENZYLIDENE 2-FLUORENAMINE, with the molecular formula C20H15N, is a chemical compound that features a benzylidene group attached to a 2-fluorenamine moiety. It is recognized for its potential applications in the field of organic chemistry, particularly in the development of new drug candidates and bioactive molecules. Due to its potential health risks, it is crucial to handle this compound with care and adhere to proper safety protocols.
Uses
Used in Pharmaceutical Industry:
BENZYLIDENE 2-FLUORENAMINE is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drug candidates and bioactive molecules.
Used in Organic Chemistry Research:
In the realm of organic chemistry, BENZYLIDENE 2-FLUORENAMINE serves as a valuable compound for research purposes, aiding in the exploration and understanding of chemical reactions and mechanisms involving benzylidene and 2-fluorenamine moieties.
Check Digit Verification of cas no
The CAS Registry Mumber 13924-50-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,9,2 and 4 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13924-50:
(7*1)+(6*3)+(5*9)+(4*2)+(3*4)+(2*5)+(1*0)=100
100 % 10 = 0
So 13924-50-0 is a valid CAS Registry Number.
InChI:InChI=1/C20H15N/c1-2-6-15(7-3-1)14-21-18-10-11-20-17(13-18)12-16-8-4-5-9-19(16)20/h1-11,13-14H,12H2/b21-14+
13924-50-0Relevant articles and documents
Iron-Catalyzed Nitrene Transfer Reaction of 4-Hydroxystilbenes with Aryl Azides: Synthesis of Imines via C=C Bond Cleavage
Peng, Yi,Fan, Yan-Hui,Li, Si-Yuan,Li, Bin,Xue, Jing,Deng, Qing-Hai
, p. 8389 - 8394 (2019/10/16)
C=C bond breaking to access the C=N bond remains an underdeveloped area. A new protocol for C=C bond cleavage of alkenes under nonoxidative conditions to produce imines via an iron-catalyzed nitrene transfer reaction of 4-hydroxystilbenes with aryl azides is reported. The success of various sequential one-pot reactions reveals that the good compatibility of this method makes it very attractive for synthetic applications. On the basis of experimental observations, a plausible reaction mechanism is also proposed.
