1282514-64-0 Usage
Molecular Structure
1H-Pyrazole-1-acetic acid, 4-[5,6-dihydro-2-[3-Methyl-1-(1-Methylethyl)-1H-1,2,4-triazol-5-yl]imidazo[1,2-d][1,4]benzoxazepin-9-yl]-α,α-diMethyl-, ethyl ester has a complex molecular structure that includes a pyrazole acetic acid core, a dihydro-2, an α,α-diMethyl group, and an ethyl ester functional group.
Pyrazole Acetic Acid Core
The compound contains a 1H-pyrazole-1-acetic acid core, which is a five-membered heterocyclic ring system with one nitrogen atom and one oxygen atom.
Dihydro-2
The compound features a dihydro-2 group, which is a saturated hydrocarbon group resulting from the addition of hydrogen to a double bond in the 2-position of the molecule.
α,α-DiMethyl Group
The compound has an α,α-diMethyl group, which consists of two methyl groups attached to the same carbon atom, contributing to the molecular complexity and potentially affecting its pharmacological properties.
Ethyl Ester Functional Group
The presence of an ethyl ester functional group in the compound suggests that it may have ester-based properties and reactivity, which could be relevant for its potential applications in medicinal chemistry.
Pharmacological and Biological Activities
The complex molecular structure of the compound suggests that it may have potential pharmacological and biological activities, although further research and analysis are needed to fully understand these properties.
Check Digit Verification of cas no
The CAS Registry Mumber 1282514-64-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,8,2,5,1 and 4 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1282514-64:
(9*1)+(8*2)+(7*8)+(6*2)+(5*5)+(4*1)+(3*4)+(2*6)+(1*4)=150
150 % 10 = 0
So 1282514-64-0 is a valid CAS Registry Number.
1282514-64-0Relevant articles and documents
Manufacture of the PI3K β-Sparing Inhibitor Taselisib. Part 2: Development of a Highly Efficient and Regioselective Late-Stage Process
St-Jean, Frédéric,Remarchuk, Travis,Angelaud, Rémy,Carrera, Diane E.,Beaudry, Danial,Malhotra, Sushant,McClory, Andrew,Kumar, Archana,Ohlenbusch, Gerd,Schuster, Andreas M.,Gosselin, Francis
, p. 783 - 793 (2019/04/01)
A highly efficient and regioselective manufacturing route for the phosphoinositide 3-kinase β-sparing inhibitor taselisib was developed. Highlights of the synthesis include: (1) magnesium-mediated formation of a challenging cyclic amidine; (2) regioselect
MUTANT SELECTIVITY AND COMBINATIONS OF A PHOSPHOINOSITIDE 3 KINASE INHIBITOR COMPOUND AND CHEMOTHERAPEUTIC AGENTS FOR THE TREATMENT OF CANCER
-
Page/Page column 85, (2014/01/08)
Methods and compositions are provided for treating hyperproliferative disorders in patients with a PI3K inhibitor, GDC-0032 as a single agent or in combination with chemotherapeutic agents.