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6-chloro-3-(3’-methoxyphenyl)coumarin is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1236360-17-0

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1236360-17-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1236360-17-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,6,3,6 and 0 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1236360-17:
(9*1)+(8*2)+(7*3)+(6*6)+(5*3)+(4*6)+(3*0)+(2*1)+(1*7)=130
130 % 10 = 0
So 1236360-17-0 is a valid CAS Registry Number.

1236360-17-0Downstream Products

1236360-17-0Relevant academic research and scientific papers

Monoamine oxidase (MAO) inhibitory activity: 3-phenylcoumarins versus 4-hydroxy-3-phenylcoumarins

Delogu, Giovanna L.,Serra, Silvia,Quezada, Elias,Uriarte, Eugenio,Vilar, Santiago,Tatonetti, Nicholas P.,Vi?a, Dolores

, p. 1672 - 1676 (2014)

Monoamine oxidase (MAO) is a useful target in the treatment of neurodegenerative diseases and depressive disorders. Both isoforms, MAO-A and MAO-B, are known to play critical roles in disease progression, and as such, the identification of novel, potent a

Synthesis and vasorelaxant and platelet antiaggregatory activities of a new series of 6-Halo-3-phenylcoumarins

Quezada, Elias,Delogu, Giovanna,Picciau, Carmen,Santana, Lourdes,Podda, Gianni,Borges, Fernanda,Garcia-Morales, Veronica,Vina, Dolores,Orallo, Francisco

experimental part, p. 270 - 279 (2010/05/18)

A series of 6-halo-3-hydroxyphenylcoumarins (resveratrol-coumarins hybrid derivatives) was synthesized in good yields by a Perkin reaction followed by hydrolysis. The new compounds were evaluated for their vasorelaxant activity in intact rat aorta rings pre-contracted with phenylephrine (PE), as well as for their inhibitory effects on platelet aggregation induced by thrombin in washed human platelets. These compounds concentration-dependently relaxed vascular smooth muscle and some of them showed a platelet antiaggregatory activity that was up to thirty times higher than that shown by trans-resveratrol and some other previously synthesized derivatives.

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