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3-(4-methylbenzyloxy)-2-pyridinecarboxaldehyde is an organic compound characterized by its molecular formula C15H13NO2. This aldehyde derivative features a pyridine ring, which is a six-membered aromatic ring containing one nitrogen atom, and a formyl group (-CHO), indicating the presence of an aldehyde functional group. The compound is further distinguished by a 4-methylbenzyl ether group attached to the pyridine ring, which consists of a benzyl group (a phenylmethyl group) with a methyl substituent. This chemical structure endows the molecule with specific reactivity and properties, making it a potential candidate for use in the synthesis of various pharmaceuticals and other organic compounds.

136423-86-4

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136423-86-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 136423-86-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,4,2 and 3 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 136423-86:
(8*1)+(7*3)+(6*6)+(5*4)+(4*2)+(3*3)+(2*8)+(1*6)=124
124 % 10 = 4
So 136423-86-4 is a valid CAS Registry Number.

136423-86-4Relevant academic research and scientific papers

Guanylhydrazones of 3-substituted 2-pyridinecarboxaldehyde and of (2-substituted 3-pyridinyloxy) acetaldehyde as prostanoid biosynthesis and platelet aggregation inhibitors

Desideri, N,Sestili, I,Manarini, S,Cerletti, C,Stein, ML

, p. 455 - 460 (2007/10/02)

Some guanylhydrazones of (3-benzyloxy)-2-pyridinecarboxaldehyde and of (2-substituted 3-pyridinyloxy)acetaldehyde were prepared in order to evaluate their possible activity as inhibitors of prostanoid biosynthesis in human serum.Only those products of the second group without the carboxylic function reduced prostanoid generation in vitro at the highest concentration; they also inhibited platelet aggregation induced by arachidonic acid and U-46619.The results suggest that these compounds are both inhibitors of cyclooxygenase and cyclic endoperoxides/TxA2 platelet receptor antagonists.

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