132274-70-5 Usage
Uses
Used in Pharmaceutical Industry:
1-Phenyl-1h-pyrazole-5-carbaldehyde is used as a key intermediate for the synthesis of various pharmaceuticals, contributing to the development of new compounds with therapeutic potential. Its unique structure allows for the creation of molecules that can target specific biological pathways, potentially leading to the discovery of novel treatments for a range of diseases and conditions.
Used in Agrochemical Industry:
In the agrochemical sector, 1-Phenyl-1h-pyrazole-5-carbaldehyde serves as a building block for the synthesis of new agrochemicals, such as pesticides and herbicides. Its reactivity and structural properties enable the design of compounds that can effectively control pests and weeds, thereby enhancing crop protection and contributing to increased agricultural productivity.
Used in Material Science:
1-Phenyl-1h-pyrazole-5-carbaldehyde is utilized in material science for the development of new materials with specific properties. Its incorporation into the molecular structure of these materials can lead to the creation of compounds with unique characteristics, such as improved stability, enhanced reactivity, or novel optical, electronic, or mechanical properties.
Used in Research and Laboratory Settings:
1-Phenyl-1h-pyrazole-5-carbaldehyde may also have potential uses in research and laboratory settings, where it can be employed as a reagent or precursor in various chemical reactions and experiments. Its unique structure and reactivity make it a valuable tool for exploring new chemical pathways and understanding the fundamental principles of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 132274-70-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,2,7 and 4 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 132274-70:
(8*1)+(7*3)+(6*2)+(5*2)+(4*7)+(3*4)+(2*7)+(1*0)=105
105 % 10 = 5
So 132274-70-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H8N2O/c13-8-10-6-7-11-12(10)9-4-2-1-3-5-9/h1-8H
132274-70-5Relevant articles and documents
Combination of two pharmacophoric systems: Synthesis and pharmacological evaluation of spirocyclic pyranopyrazoles with high σ1 receptor affinity
Schl?ger, Torsten,Schepmann, Dirk,Lehmkuhl, Kirstin,Holenz, J?rg,Vela, Jose Miguel,Buschmann, Helmut,Wünsch, Bernhard
supporting information; experimental part, p. 6704 - 6713 (2011/12/04)
The novel class of spirocyclic σ1 ligands 3 (6′,7′-dihydro-1′H-spiro[piperidine-4,4′-pyrano[4,3-c] pyrazoles]) was designed by the combination of the potent σ1 ligands 1 and 2 in one molecule. Thorough structure affinity relationship
Synthesis and structure-affinity relationships of novel spirocyclic σ receptor ligands with furopyrazole structure
Schlaeger, Torsten,Schepmann, Dirk,Wuerthwein, Ernst-Ulrich,Wuensch, Bernhard
, p. 2992 - 3001 (2008/09/20)
The synthesis of novel spirocyclic σ receptor ligands with high affinity is described. The cyclization of the hydroxy acetal 8, which represents a key step in the synthesis of the spirocyclic compounds 3, was supported by theoretical considerations. The a
Spiro-pyrano-pyrazole derivatives
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Page/Page column 13-14; 18-19, (2008/12/04)
The present invention relates to compounds of formula (I) having pharmacological activity towards the sigma (σ) receptor, and more particularly to some spiro-pyrano-pyrazole derivatives, to processes of preparation of such compounds, to pharmaceutical com
Cycloadditions with 1-Phenyl-5-vinylpyrazole
Medio-Simon, Mercedes,Laviada, M. Jose Alvarez de,Sequlveda-Arques, Jose
, p. 2749 - 2750 (2007/10/02)
1-Phenyl-5-vinylpyrazole reacts with dimethylacetylenedicarboxylate (DMAD), N-phenylmaleimide (NPMI), tetracyanoethylene (TCNE), 4-phenyl-1,2,4-triazoline-3,5-dione (PTAD), and diethyl azodicarboxylate (DEAZD) to afford 1:1 adducts through Diels-Alder cyc
