93477-21-5 Usage
Description
1-(4-methyl-1-phenylpent-1-yn-3-yl)piperidine is a chemical compound with the molecular formula C18H23N. It is a piperidine derivative that contains a phenyl group and an alkyne group. 1-(4-methyl-1-phenylpent-1-yn-3-yl)piperidine is characterized by its unique structure, which contributes to its potential pharmacological properties and makes it a valuable building block for the synthesis of various bioactive compounds.
Uses
Used in Organic Synthesis:
1-(4-methyl-1-phenylpent-1-yn-3-yl)piperidine is used as a key intermediate in organic synthesis for the creation of complex molecular structures. Its unique combination of functional groups allows for versatile chemical reactions, making it a valuable component in the synthesis of a wide range of compounds.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 1-(4-methyl-1-phenylpent-1-yn-3-yl)piperidine is used as a starting material for the development of new drugs. Its structure and properties make it a promising candidate for the design and synthesis of novel bioactive molecules with potential therapeutic applications.
Used in Pharmaceutical Industry:
1-(4-methyl-1-phenylpent-1-yn-3-yl)piperidine is used as a building block for the development of new medications in the pharmaceutical industry. Its potential pharmacological properties and structural diversity make it a valuable asset in the search for new treatments for various conditions.
Used in Drug Development:
1-(4-methyl-1-phenylpent-1-yn-3-yl)piperidine is used as a precursor in drug development, where its unique structure can be exploited to create new drugs with improved efficacy and selectivity. Its potential use in the development of new medications for various conditions highlights its importance in the field of medicinal chemistry and pharmaceutical research.
Check Digit Verification of cas no
The CAS Registry Mumber 93477-21-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,4,7 and 7 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 93477-21:
(7*9)+(6*3)+(5*4)+(4*7)+(3*7)+(2*2)+(1*1)=155
155 % 10 = 5
So 93477-21-5 is a valid CAS Registry Number.
93477-21-5Relevant articles and documents
Synthesis and characterization of magnetic glycocyamine-modified chitosan as a biosupport for the copper immobilization and its catalytic activity investigation
Rafiee,Karder, F. Rezaie
, (2019/11/29)
Trichloro-1,3,5-triazine agent was used for chitosan functionalization and as a bridge between the functionalized chitosan and glycocyamine to form a bio ligand for the copper coordination. The magnetization of modified chitosan was done using of Fe3
Construction of polymeric Cu(I) N-heterocyclic carbene complex utilizing terpyridine-Fe(II) as linkers: formation of an efficient and recyclable catalyst
Yang, Jin
, p. 155 - 163 (2018/02/09)
A metal-coordination-driven self-assembly using the predesigned building block has been developed. Herein, the catalytic active NHC–Cu(I) units were introduced into the terpyridine metal coordination polymers. The self-assembled architecture, as a heterog
Based on double-pyrazole methyl phenoxy methyl imidazole nitrogen heterocyclic cabeen silver complex and its preparation method and application
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Paragraph 0031-0033, (2017/01/17)
The invention relates to a nitrogen heterocyclic carbene silver complex based on bispyrazole methyl phenoxy methylimidazole and a preparation method and application thereof. The preparation method of the nitrogen heterocyclic carbene silver complex is as follows: at room temperature in dark conditions, a bispyrazole methyl phenoxy methyl substituted imidazolium salt and silver oxide in the molar ratio of 1 to 0.7 are dissolved in an organic solvent for reaction for 24 hours, then filtered and concentrated to prepare the nitrogen heterocyclic carbene silver complex. The nitrogen heterocyclic carbene silver complex has strong capability of emission fluorescence and catalyzing of coupled reaction of acetylene, amine and aldehyde three components, and can be mainly used in fluorescent materials and organic catalysis technology field.
