1227068-67-8 Usage
Description
1-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-5,6-dihydropyridin-1(2h)-yl)ethanone is a highly specific chemical compound primarily used in synthetic chemistry. It features a complex structure that includes a dioxaborolane and dihydropyridine group. The presence of the tetramethyl dioxaborolane component indicates that this compound can be employed in boron-aided chemical reactions, such as the Suzuki reaction, which is a widely used method for forming carbon-carbon bonds. Due to its intricate structure, the synthesis of this chemical is typically complex and is generally reserved for specialized industrial or academic research settings. 1-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-5,6-dihydropyridin-1(2h)-yl)ethanone's properties, including its potential for corrosion, environmental impact, and health effects, are contingent upon the specific conditions of its synthesis and application.
Uses
Used in Synthetic Chemistry:
1-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-5,6-dihydropyridin-1(2h)-yl)ethanone is used as a synthetic intermediate for facilitating complex chemical reactions, particularly in the context of the Suzuki reaction. This reaction is a cross-coupling process that allows for the formation of carbon-carbon bonds, which is crucial for the synthesis of various organic compounds.
Used in Academic Research:
In academic research, 1-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-5,6-dihydropyridin-1(2h)-yl)ethanone is employed as a specialized reagent for studying the mechanisms and outcomes of boron-aided chemical reactions. Its unique structure provides researchers with insights into the behavior of dioxaborolane and dihydropyridine groups in various chemical processes.
Used in Industrial Applications:
1-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-5,6-dihydropyridin-1(2h)-yl)ethanone is utilized in industrial applications where the creation of specific organic compounds requires the use of advanced synthetic methods. Its role in these processes is to act as a key component in the synthesis of complex molecules, contributing to the development of new materials and pharmaceuticals.
Check Digit Verification of cas no
The CAS Registry Mumber 1227068-67-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,7,0,6 and 8 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1227068-67:
(9*1)+(8*2)+(7*2)+(6*7)+(5*0)+(4*6)+(3*8)+(2*6)+(1*7)=148
148 % 10 = 8
So 1227068-67-8 is a valid CAS Registry Number.
InChI:InChI=1S/C13H22BNO3/c1-10(16)15-8-6-11(7-9-15)14-17-12(2,3)13(4,5)18-14/h6H,7-9H2,1-5H3
1227068-67-8Relevant articles and documents
TROPOLONE DERIVATIVES AND TAUTOMERS THEREOF FOR IRON REGULATION IN ANIMALS
-
, (2021/04/23)
Disclosed are a series of compounds or their tautomers having a general structure represented by Formula (la), (lb), (Ila), (lIb), or (lIc) and pharmaceutically acceptable salts thereof. The present disclosure also relates to pharmaceutical compositions comprising said compounds or tautomers. The present disclosure further relates to a method of treating a disease or condition associated with iron dysregulation or dysfunctional iron homeostasis comprising administering to a subject in need thereof a therapeutically effective amount of Formula (la), (lb), (Ila), (lIb), or (lIc) compounds or tautomers.
Substituted Indoles
-
Paragraph 0649, (2017/07/14)
The invention provides for compounds of formula (I) wherein R1, R2, R3, R4, R5, and R6 have any of the values defined in the specification, and pharmaceutically acceptable salts thereof, th
ISOCHROMENE DERIVATIVES AS PHOSHOINOSITIDE 3-KINASES INHIBITORS
-
, (2015/06/24)
Compounds of formula (I) described herein are useful for inhibiting phosphoinositide 3-kinases (PI3K) and the treatment of disorders associated with PI3K enzymes.
