153687-35-5 Usage
General Description
1-(4-Methoxy-benzyl)-1H-pyrazole-4-carbaldehyde is a chemical compound with the molecular formula C12H12N2O2. It belongs to the class of pyrazole derivatives and contains a benzyl group, a methoxy group, and an aldehyde functional group. 1-(4-Methoxy-benzyl)-1H-pyrazole-4-carbaldehyde has potential applications in organic synthesis and medicinal chemistry. Its structure suggests that it could be used as a building block for the synthesis of more complex molecules, and it may also have biological activity due to its structural features. Further research and testing would be needed to determine its specific uses and potential benefits.
Check Digit Verification of cas no
The CAS Registry Mumber 153687-35-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,6,8 and 7 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 153687-35:
(8*1)+(7*5)+(6*3)+(5*6)+(4*8)+(3*7)+(2*3)+(1*5)=155
155 % 10 = 5
So 153687-35-5 is a valid CAS Registry Number.
153687-35-5Relevant articles and documents
SMYD INHIBITORS
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Paragraph 1087; 1090-1092, (2017/07/18)
The present disclosure provides carboxamides and sulfonamides having Formula (I): and the pharmaceutically acceptable salts and solvates thereof, wherein A, Y, B, X, and Z are defined as set forth in the specification. The present disclosure is also directed to the use of compounds of Formula (I) to treat a disorder responsive to the blockade of SMYD proteins such as SMYD3 or SMYD2. Compounds of the present disclosure are especially useful for treating cancer.
Porphyrins with four azole substituents in meso positions: X-ray crystal structure of meso-tetrakis-(1-benzylpyrazol-4-yl)-porphyrin at 200 K
Werner, Andreas,Sanchez-Migallon, Ana,Fruchier, Alain,Elguero, Jose,Fernandez-Castano, Cristina,Foces-Foces, Concepcion
, p. 4779 - 4800 (2007/10/02)
Several new porphyrins have been prepared in improved yields using an established method which was adapted to formylpyrazoles bearing on the pyrazole N1-nitrogen protective groups. The deprotection of N-para-methoxybenzyl and SEM protected meso
