7223-42-9 Usage
Uses
Used in Pharmaceutical Industry:
3-(PROP-2-YN-1-YLOXY)PYRIDINE is used as a key intermediate in the synthesis of pharmaceutical compounds for its ability to participate in various chemical reactions, facilitating the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 3-(PROP-2-YN-1-YLOXY)PYRIDINE serves as a crucial component in the production of agrochemicals, leveraging its reactivity to create compounds that can be used in pest control and crop protection.
Used in Organic Synthesis:
3-(PROP-2-YN-1-YLOXY)PYRIDINE is utilized as a versatile building block in organic synthesis for its capacity to undergo multiple types of chemical reactions, contributing to the creation of a wide array of chemical products, including fine chemicals with specific applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 7223-42-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,2 and 3 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7223-42:
(6*7)+(5*2)+(4*2)+(3*3)+(2*4)+(1*2)=79
79 % 10 = 9
So 7223-42-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H11N/c1-2-5-8-6-3-4-7-8/h1H,3-7H2
7223-42-9Relevant academic research and scientific papers
Solvent-dependent competitive rearrangements of cyclic tertiary propargylamine N-oxides
Szabo, Anna,Galstnibos-Farago, Agnes,Mucsi, Zoltan,Timari, Geza,Vasvari-Debreczy, Lelle,Hermecz, Istvan
, p. 687 - 694 (2007/10/03)
In protic media, cyclic propargylamine N-oxides 1 undergo solvent-dependent competitive rearrangements leading to enamino aldehydes 5, acrylamides 3, and secondary amines 4. The ratios of the products are evaluated and the possible mechanism of the compet
The stability of butinoline
Unterhalt,Middelberg
, p. 492 - 494 (2007/10/02)
The stability of butinoline in alkaline and acidic solution was investigated. In alkaline solution the retrosynthesis to benzophenone and 3-pyrrolidino-1-propin was observed, in acidic solution the Meyer-Schuster rearrangement to the corresponding unsaturated amino ketone took place. Thermolysis gave 1,1-diphenyl-2-butin-1-ol in addition to the products of retrosynthesis.
