18201-87-1 Usage
Molecular structure
A benzene ring with a nitrile group (C≡N) attached to the 2nd carbon, and a 4-fluorophenylamino group attached to the 1st carbon.
Molecular structure
An anthracene core with a nitrile group (C≡N) attached to the 9th carbon, and a p-fluorophenyl group attached to the nitrogen atom.
Functional groups
Nitrile group, amino group, and fluorophenyl group.
Functional groups
Nitrile group, anthracene core, and fluorophenyl group.
Physical state
Solid.
Physical state
Solid.
Applications
Building block in organic synthesis, pharmaceuticals, and potential use in new materials and chemical reagents.
Applications
Building block in organic synthesis, pharmaceuticals, and potential use in new materials and chemical reagents.
Check Digit Verification of cas no
The CAS Registry Mumber 18201-87-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,2,0 and 1 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 18201-87:
(7*1)+(6*8)+(5*2)+(4*0)+(3*1)+(2*8)+(1*7)=91
91 % 10 = 1
So 18201-87-1 is a valid CAS Registry Number.
18201-87-1Relevant articles and documents
NON-FUSED TRICYCLIC COMPOUNDS
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Paragraph 00311, (2018/11/26)
Provided herein are compounds and pharmaceutical compositions comprising said compounds that are useful for treating cancers. Specific cancers include those that are mediated by YAP/TAZ or those that are modulated by the interaction between YAP/TAZ and TEAD.
Rhodium(III)-Catalyzed Direct Cyanation of Aromatic C-H Bond to Form 2-(Alkylamino)benzonitriles Using N-Nitroso As Directing Group
Dong, Jiawei,Wu, Zhongjie,Liu, Zhengyi,Liu, Ping,Sun, Peipei
, p. 12588 - 12593 (2016/01/09)
2-(Alkylamino)benzonitriles were synthesized via a rhodium-catalyzed cyanation on the aryl C-H bond and subsequent denitrosation of N-nitrosoarylamines using a removable nitroso as the directing group, in which N-cyano-N-phenyl-p-methylbenzenesulfonamide (NCTS) was used as the "CN" source. Various substituents on the aryl ring and amino group of N-nitrosoarylamines tolerated the reaction, and the corresponding products were achieved in moderate to good yields.
