906811-49-2 Usage
Description
Benzenemethanol, 2-amino-3-fluoro(9CI) is a chemical compound with the molecular formula C7H8FNO. It is a derivative of benzenemethanol with an amino group and a fluorine atom attached to the ring. Benzenemethanol, 2-amino-3-fluoro(9CI) is known for its potential biological activity and therapeutic applications, making it a valuable asset in pharmaceutical research and drug development.
Uses
Used in Pharmaceutical Research and Drug Development:
Benzenemethanol, 2-amino-3-fluoro(9CI) is utilized as a key component in the development of new pharmaceuticals due to its potential biological activity. Its unique structure allows it to interact with various biological targets, offering a wide range of therapeutic applications.
Used as a Building Block in Organic Synthesis:
In addition to its pharmaceutical applications, Benzenemethanol, 2-amino-3-fluoro(9CI) also serves as a building block in the synthesis of various organic compounds. Its versatile structure enables it to be incorporated into a multitude of chemical reactions, contributing to the creation of new and innovative molecules for various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 906811-49-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,6,8,1 and 1 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 906811-49:
(8*9)+(7*0)+(6*6)+(5*8)+(4*1)+(3*1)+(2*4)+(1*9)=172
172 % 10 = 2
So 906811-49-2 is a valid CAS Registry Number.
906811-49-2Relevant articles and documents
Enantioconvergent Amination of Racemic Tertiary C-H Bonds
Lang, Kai,Li, Chaoqun,Kim, Isaac,Zhang, X. Peter
supporting information, p. 20902 - 20911 (2020/12/22)
Racemization is considered to be an intrinsic stereochemical feature of free radical chemistry as can be seen in traditional radical halogenation reactions of optically active tertiary C-H bonds. If the facile process of radical racemization could be effe
Catalytic Asymmetric [4 + 3] Annulation of C, N-Cyclic Azomethine Imines with Copper Allenylidenes
Wang, Yanfang,Zhu, Liping,Wang, Mengran,Xiong, Jiale,Chen, Nannan,Feng, Xing,Xu, Zhaoqing,Jiang, Xianxing
supporting information, p. 6506 - 6510 (2018/10/20)
The first asymmetric decarboxylative [4 + 3] annulation of propargylic carbamates with C,N-cyclic azomethine imines has been developed successfully by a copper-N-heterocyclic carbine system. This strategy led to a series of optically active isoquinoline-f
HUMAN PLASMA KALLIKREIN INHIBITORS
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Page/Page column 382; 383, (2015/11/02)
Disclosed are compounds of formula (I), as described herein, and pharmaceutically acceptable salts thereof. The compounds are inhibitors of plasma kallikrein. Also provided are pharmaceutical compositions comprising at least one compound of the invention, and methods involving use of the compounds and compositions of the invention in the treatment and prevention of diseases and conditions characterized by unwanted plasma kallikrein activity.