6323-79-1 Usage
Description
3-DI-N-PROPYLAMINO-1-PROPYNE is a propargylamine derivative that features a terminal alkyne group and a N-PROPYLAMINO group. It is a chemical compound known for its unique reactivity and compatibility with various functional groups, making it a valuable reagent in organic synthesis. 3-DI-N-PROPYLAMINO-1-PROPYNE is also recognized for its potential in pharmaceutical research, where it can be utilized as a building block for the synthesis of biologically active molecules. Furthermore, it has been explored for its applications in materials science and in the development of innovative chemical reactions. However, due to the high reactivity of alkyne compounds, it is crucial to handle 3-DI-N-PROPYLAMINO-1-PROPYNE with care to avoid potential hazards.
Uses
Used in Pharmaceutical Research:
3-DI-N-PROPYLAMINO-1-PROPYNE is used as a building block for the synthesis of biologically active compounds, contributing to the development of new pharmaceutical agents.
Used in Organic Synthesis:
3-DI-N-PROPYLAMINO-1-PROPYNE is used as a reagent in various organic synthesis reactions due to its unique reactivity and functional group compatibility, facilitating the creation of diverse chemical structures.
Used in Materials Science:
3-DI-N-PROPYLAMINO-1-PROPYNE is used in the study and development of new materials, leveraging its chemical properties to enhance material characteristics.
Used in Chemical Reaction Development:
3-DI-N-PROPYLAMINO-1-PROPYNE is used as a reagent in the development of new chemical reactions, expanding the scope of synthetic chemistry and potentially leading to more efficient or novel synthetic pathways.
Check Digit Verification of cas no
The CAS Registry Mumber 6323-79-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,2 and 3 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6323-79:
(6*6)+(5*3)+(4*2)+(3*3)+(2*7)+(1*9)=91
91 % 10 = 1
So 6323-79-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H17N/c1-4-7-10(8-5-2)9-6-3/h1H,5-9H2,2-3H3
6323-79-1Relevant articles and documents
Synthesis, biological evaluation and molecular modeling of novel triazole-containing berberine derivatives as acetylcholinesterase and β-amyloid aggregation inhibitors
Shi, Anding,Huang, Ling,Lu, Chuanjun,He, Feng,Li, Xingshu
experimental part, p. 2298 - 2305 (2011/05/07)
A series of novel triazole-containing berberine derivatives were synthesized via the azide-alkyne cycloaddition reaction. Their biological activity as inhibitors of both acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE) were evaluated. Among t
Acetylenes as Potential Antarafacial Components in Concerted Reactions. Formation of Pyrroles from Thermolyses of Propargylamines, of a Dihydrofuran from a Propargylic Ether, and of an Ethylidenepyrrolidine from a β-Amino Acetylene
Viola, Alfred,Collins, John J.,Filipp, Nicholas,Locke, John S.
, p. 5067 - 5075 (2007/10/02)
A thermal cyclization of acetylenic compounds provides evidence for the ability of acetylenic links to act as antarafacial components in processes.The cyclization competes with the normally favored acetylenic retro-ene reaction.Propargylic amines, without substituents whose presence would hinder a tight cyclic transition state, yield intermediate pyrrolines whose subsequent hydrogen elimination affords pyrroles in small amounts.The same process in 2-ethynyltetrahydropyran affords 8-oxabicyclooctane in 35percent yield.A related thermal reaction of N-methyl-3-hexyn-1-amine provides a quantitative transformation to N-methyl-2-ethylidenepyrrolidine in a nominal s + 2a + 2s + 2s> Moebius process, wherein the acetylenic unit is the antarafacial component.Evidence for concertedness in these reactions is discussed.
