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6-Chloro-2-(4-chloro-phenyl)-thiochromen-4-one is a complex organic chemical compound with the molecular formula C14H7Cl2OS. It is a derivative of thiochromen-4-one, which is a type of heterocyclic compound containing a sulfur atom. The molecule features a thiochromenone ring system with a chlorine atom at the 6-position and a 4-chlorophenyl group attached at the 2-position. 6-chloro-2-(4-chloro-phenyl)-thiochromen-4-one is known for its potential applications in the synthesis of pharmaceuticals and agrochemicals, particularly as an intermediate in the production of various biologically active molecules. Its chemical structure and properties make it a valuable component in the development of new drugs and pesticides, although its specific uses and safety profile would require further investigation and testing.

790-15-8

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790-15-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 790-15-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,9 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 790-15:
(5*7)+(4*9)+(3*0)+(2*1)+(1*5)=78
78 % 10 = 8
So 790-15-8 is a valid CAS Registry Number.

790-15-8Downstream Products

790-15-8Relevant academic research and scientific papers

Antimalarial and anticoccidial activity of 3-aryl-7-chloro-3,4-dihydroacridine-1,9-(2H,10H)-diones. 1-Imines, 1-amines, 1-oximes, 1-hydrazones and related compounds

Winkelmann,Raether

, p. 647 - 661 (2007/10/02)

Out of more than 130 synthesized derivatives of floxacrine and of 10-deoxyfloxacrine, such as 3-(4-trifluoromethyl-phenyl) or 3-(4-chlorophenyl)-7-chloro-10-hydroxy- or -10-deoxy-3,4-dihydroacridine-1,9(2H,10H)-dione 1-imines and 1-hydrazones, more than 4

A new class of antimalarial drugs: Derivatives of benzothiopyrans

Razdan,Bruni,Mehta,Weinhardt,Papanastassiou

, p. 643 - 649 (2007/10/05)

A series of substituted benzothiopyrans was synthesized and examined for antimalarial activity. Some were found to be active and curative at dose levels of 160 - 360 mg/kg against Plasmodium berghei in mice. A few observations concerning structure-activity relationships were made. The benzothiopyrans were prepared by treatment of either the gem-dichloro- or the thionothioflavone intermediate with various primary amines. The thionothioflavone intermediates were made from thioflavones. Condensation of thiophenols with benzoyl acetates gave the thioflavones.

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