725746-81-6 Usage
Pyrazole derivative
It is a five-membered heterocyclic compound 1-Isobutyl-1H-pyrazole is derived from the pyrazole structure, which is a five-membered ring containing two nitrogen atoms at positions 1 and 2.
Isobutyl group
The compound contains an isobutyl group (C4H9) 1-Isobutyl-1H-pyrazole has an isobutyl group attached to the pyrazole ring, which contributes to its chemical properties and reactivity.
Building block in organic synthesis
Commonly used in pharmaceutical and agrochemical industries 1-Isobutyl-1H-pyrazole is often employed as a starting material for the synthesis of various bioactive molecules and pharmaceutical drugs in both pharmaceutical and agrochemical industries.
Synthesis of bioactive molecules
Can be used to create pharmaceutical drugs 1-Isobutyl-1H-pyrazole can be utilized as a starting material for the synthesis of different pharmaceutical drugs, showcasing its versatility in organic synthesis.
Potential biological activities
Antitumor and antimicrobial properties Research has been conducted on 1-Isobutyl-1H-pyrazole to explore its possible biological activities, including its potential as an antitumor and antimicrobial agent.
Research and development
Used as a reagent or intermediate for the production of other organic compounds 1-Isobutyl-1H-pyrazole may also be employed in research and development settings as a reagent or intermediate for synthesizing other organic compounds, highlighting its importance in chemical research.
Check Digit Verification of cas no
The CAS Registry Mumber 725746-81-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,2,5,7,4 and 6 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 725746-81:
(8*7)+(7*2)+(6*5)+(5*7)+(4*4)+(3*6)+(2*8)+(1*1)=186
186 % 10 = 6
So 725746-81-6 is a valid CAS Registry Number.
725746-81-6Relevant articles and documents
2-PHENYL INDENE DERIVATIVES USEFUL AS ESTROGEN RECEPTOR LIGANDS
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Page/Page column 65, (2008/06/13)
The invention provides a compound of formula (I) or a pharmaceutically acceptable ester, amide, solvate or salt thereof, including a salt of such an ester or amide, and a solvate of such an ester, amide or salt. The invention also provides also provides the use of such compounds in the treatment or prophylaxis of a condition associated with a disease or disorder associated with estrogen receptor activity. Formula (I), wherein R1, R2, R3, R4, R5, R6, R7, R8, R9, R10, R11 and R12 are as defined in the specification, and wherein either the bond between the C1and C2 carbon atoms is a double bond or the bond between the C2 and C3 carbon atoms is a double bond, R2 being absent when the bond between the C1 and C2 carbon atoms is a double bond.
Synthesis of pinacol esters of 1-alkyl-1H-pyrazol-5-yl- and 1-alkyl-1H-pyrazol-4-ylboronic acids
Ivachtchenko, Alexandre V.,Kravchenko, Dmitry V.,Zheludeva, Valentina I.,Pershin, Dmitry G.
, p. 931 - 939 (2007/10/03)
Starting from 1H-pyrazol, a wide number of 1-alkyl-1H-pyrazol-4-yl and 1-alkyl-1H-pyrazol-5-ylboronic acids and their pinacol esters were synthesized and characterized. The key step in the described methodology is the regioselective lithiation of the pyrazole ring. The synthesized pinacolates are stable under prolonged storage and can be used as convenient reagents in organic synthesis.
