146019-45-6 Usage
Description
(4-AMINO-3-FLUORO-PHENYL)-METHANOL is a chemical compound with the molecular formula C7H7FNO. It is a derivative of phenol and contains both an amino group and a fluorine atom. (4-AMINO-3-FLUORO-PHENYL)-METHANOL has unique properties due to the presence of the fluorine atom, making it a versatile building block in the synthesis of more complex organic molecules.
Uses
Used in Pharmaceutical Synthesis:
(4-AMINO-3-FLUORO-PHENYL)-METHANOL is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs with improved properties.
Used in Agrochemical Synthesis:
In the agrochemical industry, (4-AMINO-3-FLUORO-PHENYL)-METHANOL is used as a precursor in the production of various agrochemicals, potentially enhancing the effectiveness of these products.
Used in Materials Science:
(4-AMINO-3-FLUORO-PHENYL)-METHANOL is utilized as a component in the development of new materials, taking advantage of its unique chemical properties to create innovative material solutions.
Used in Organic Electronics:
(4-AMINO-3-FLUORO-PHENYL)-METHANOL is also used in the field of organic electronics, where its properties can be harnessed to improve the performance of electronic devices and components.
Overall, (4-AMINO-3-FLUORO-PHENYL)-METHANOL has diverse and important applications in the field of chemistry and related industries, making it a valuable compound for research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 146019-45-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,0,1 and 9 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 146019-45:
(8*1)+(7*4)+(6*6)+(5*0)+(4*1)+(3*9)+(2*4)+(1*5)=116
116 % 10 = 6
So 146019-45-6 is a valid CAS Registry Number.
146019-45-6Relevant articles and documents
Mechanistic Evaluation of Bioorthogonal Decaging with trans-Cyclooctene: The Effect of Fluorine Substituents on Aryl Azide Reactivity and Decaging from the 1,2,3-Triazoline
Matikonda, Siddharth S.,Fairhall, Jessica M.,Fiedler, Franziska,Sanhajariya, Suchaya,Tucker, Robert A. J.,Hook, Sarah,Garden, Anna L.,Gamble, Allan B.
, p. 324 - 334 (2018/02/28)
Bioorthogonal prodrug activation/decaging strategies need to be selective, rapid and release the drug from the masking group upon activation. The rates of the 1,3-dipolar cycloaddition between a trans-cyclooctene (TCO) and a series of fluorine-substituted
HUMAN PLASMA KALLIKREIN INHIBITORS
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Page/Page column 151; 152, (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.