1044270-96-3 Usage
Uses
Used in Organic Synthesis:
3-bromo-1-(oxan-2-yl)-1H-pyrazole is used as a synthetic intermediate for the creation of various organic compounds. Its unique structure allows for the formation of new chemical bonds and the synthesis of a wide range of molecules.
Used in Pharmaceutical Industry:
3-bromo-1-(oxan-2-yl)-1H-pyrazole is used as a potential drug candidate in the pharmaceutical industry. Its structure and properties may contribute to the development of new medications for the treatment of various diseases and conditions.
Used in Agrochemicals:
3-bromo-1-(oxan-2-yl)-1H-pyrazole is used as a building block for the development of agrochemicals, such as pesticides and herbicides. Its unique structure and properties can be harnessed to create effective and environmentally friendly solutions for agricultural applications.
Further research into the potential uses and properties of 3-bromo-1-(oxan-2-yl)-1H-pyrazole could lead to its application in various fields of chemistry and medicine, expanding its utility and impact on society.
Check Digit Verification of cas no
The CAS Registry Mumber 1044270-96-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,4,2,7 and 0 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1044270-96:
(9*1)+(8*0)+(7*4)+(6*4)+(5*2)+(4*7)+(3*0)+(2*9)+(1*6)=123
123 % 10 = 3
So 1044270-96-3 is a valid CAS Registry Number.
1044270-96-3Relevant articles and documents
INHIBITORS OF ENL/AF9 YEATS
-
Paragraph 00143-00144; 00455-00456, (2021/06/26)
Methods and compositions for treating leukemia are disclosed. Acylated 6-aminoindoles, acylated 6-aminopyrrolopyridines and acylated 3-aminopyrrolo[3,2-c]pyridazines of the following formula inhibit ENL/AF9 YEATS and are therefore useful for treating leukemia.
METHODS FOR THE PREPARATION OF 5-BROMO-2-(3-CHLORO-PYRIDIN-2-YL)-2H-PYRAZOLE-3-CARBOXYLIC ACID
-
Paragraph 0289; 0290, (2021/04/23)
Described herein are novel methods of synthesizing 5-Bromo-2-(3-chloro-pyridin-2-yl)- 2H-pyrazole-3-carboxylic acid from pyrazole or pyrazole derivatives.