110525-57-0 Usage
General Description
1-[(4-Nitrophenyl)methyl]pyrazole is a chemical compound with the molecular formula C11H9N3O2. It is a pyrazole derivative with a nitrophenyl group attached to the methyl group. 1-[(4-Nitrophenyl)methyl]pyrazole is commonly used in organic synthesis and pharmaceutical research due to its unique structure and potential biological activities. It has been investigated for its potential as an anti-inflammatory and analgesic agent. Additionally, 1-[(4-Nitrophenyl)methyl]pyrazole is also used in the development of new materials and as a building block for the synthesis of more complex organic compounds. Its versatility and potential applications make it an important compound in the field of organic chemistry and pharmaceutical research.
Check Digit Verification of cas no
The CAS Registry Mumber 110525-57-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,5,2 and 5 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 110525-57:
(8*1)+(7*1)+(6*0)+(5*5)+(4*2)+(3*5)+(2*5)+(1*7)=80
80 % 10 = 0
So 110525-57-0 is a valid CAS Registry Number.
110525-57-0Relevant articles and documents
Synthesis of 1-(p-nitrobenzyl)azoles and 1-(p-nitrobenzyl)benzazoles
Pardo, Carmen,Graf, Sabine,Ramos, Mar,Sesmilo, Esther,Elguero, Jose
, p. 385 - 390 (2000)
-
Suzuki-miyaura cross-coupling of potassium trifluoro(N -methylheteroaryl) borates with aryl and heteroaryl halides
Molander, Gary A.,Ryu, Daweon,Hosseini-Sarvari, Mona,Devulapally, Rammohan,Seapy, Dave G.
, p. 6648 - 6656 (2013/07/26)
The synthesis of potassium trifluoro(N-methylheteroaryl)borates and their use in cross-coupling reactions with various aryl and heteroaryl halides to construct N-methyl heteroaryl-substituted aromatic and heteroaromatic compounds are reported.
SUBSTITUTION NUCLEOPHYLE RADICALAIRE EN CHAINE (SRN1). 16eme MEMOIRE: N-ALCOYLATION DE L'IMIDAZOLE, DU BENZIMIDAZOLE, DU PYRRAZOLE ET DU TRIAZOLE
Beugelmans, Rene,Lechevalier, Andre
, p. 6209 - 6212 (2007/10/02)
The title amines behave as nucleophiles towards p-nitrobenzylchloride or variously funtionnalyzed gem-halo nitro alkanes in reactions responding to the classical criteria for the SRN1 mechanism.
