815608-06-1 Usage
Description
1-(1-ethoxyethyl)-1H-pyrazole-4-carbaldehyde is a chemical compound characterized by the molecular formula C10H14N2O2. It is a derivative of the pyrazole class, featuring a carbaldehyde functional group and an ethoxyethyl substituent. 1-(1-ethoxyethyl)-1H-pyrazole-4-carbaldehyde is known for its role in the synthesis of various pharmacologically active molecules and serves as an intermediate in the production of pharmaceuticals and agrochemicals.
Uses
Used in Organic Synthesis:
1-(1-ethoxyethyl)-1H-pyrazole-4-carbaldehyde is used as a building block in the organic synthesis industry for the preparation of a wide range of pharmacologically active molecules. Its unique structure allows for the creation of diverse chemical entities with potential therapeutic applications.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 1-(1-ethoxyethyl)-1H-pyrazole-4-carbaldehyde is utilized as an intermediate in the development and manufacturing of various drugs. Its presence in the synthesis process contributes to the formation of bioactive compounds with specific therapeutic properties.
Used in Agrochemicals:
1-(1-ethoxyethyl)-1H-pyrazole-4-carbaldehyde also finds application in the agrochemical sector, where it is employed as an intermediate in the synthesis of compounds with pesticidal or herbicidal properties, contributing to the development of more effective and targeted agricultural products.
Used in Research and Laboratory Settings:
1-(1-ethoxyethyl)-1H-pyrazole-4-carbaldehyde is also used in research and laboratory settings to investigate the properties and reactivity of pyrazole derivatives. Its study aids in understanding the behavior of similar compounds and can lead to the discovery of new applications in various fields.
Potential Applications in Material and Chemical Technology Development:
1-(1-ethoxyethyl)-1H-pyrazole-4-carbaldehyde may have future applications in the development of new materials and chemical technologies, given its unique structural features and reactivity. Its potential in this area is currently under exploration and may lead to innovative advancements in material science and chemical engineering.
Check Digit Verification of cas no
The CAS Registry Mumber 815608-06-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,1,5,6,0 and 8 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 815608-06:
(8*8)+(7*1)+(6*5)+(5*6)+(4*0)+(3*8)+(2*0)+(1*6)=161
161 % 10 = 1
So 815608-06-1 is a valid CAS Registry Number.
815608-06-1Relevant articles and documents
Synthesis of substituted-3-iodo-1H-pyrazole derivatives and their further modification under Sonogashira cross-coupling reaction conditions
Mazeikaite, Rita,Sudzius, Jurgis,Urbelis, Gintaras,Labanauskas, Linas
, p. 54 - 71 (2014/12/10)
A convenient synthetic route for preparation of valuable synthetic intermediates - 1-(1-ethoxyethyl)-3-iodo-1H-pyrazole derivatives has been developed. During this work protection reaction of N-H bond in substituted 3-iodo-1H-pyrazole derivatives with ethyl vinyl ether and migration of ethoxyethyl protecting group was investigated. Synthetic possibilities of Sonogashira cross-coupling reactions of substituted 1-(1-ethoxyethyl)-3-iodo-1H-pyrazole derivatives with phenylacetylene were studied and evaluated.
A multifunctional high-spin biradical pyrazolylbipyridine- bisnitronylnitroxide
Zoppellaro, Giorgio,Enkelmann, Volker,Geies, Ahmed,Baumgarten, Martin
, p. 4929 - 4932 (2007/10/03)
(Chemical Equation Presented) Synthesis and UV-vis, IR, and EPR spectroscopic characterizations, together with X-ray structural analysis, of functional nitronyl- and iminonitroxides attached to pyrazolylbipyridine are described. The exchange interactions between the nitronylnitroxides are found to be stronger than for the iminonitroxides. Although the substitution of a pyridine with the pyrazole ring leads to shorter distances and larger dipolar couplings, the exchange interaction is diminished. While compound 1 forms dimers in the solid state, the terpyridine 3 leads to supramolecular π-stacking.
