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Dihydro-5-(4-chlorophenyl)-2(3H)-thiophenone is a chemical compound with the molecular formula C10H9ClOS. It is a derivative of thiophene, a heterocyclic compound consisting of a five-membered ring with one sulfur atom and four carbon atoms. The compound features a 4-chlorophenyl group attached to the thiophene ring, which imparts a chlorine atom to the phenyl ring. This chemical is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly those containing the thiophene moiety. Its chemical structure and properties make it a versatile building block for the development of new compounds with potential applications in various industries.

4521-17-9

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4521-17-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4521-17-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,2 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4521-17:
(6*4)+(5*5)+(4*2)+(3*1)+(2*1)+(1*7)=69
69 % 10 = 9
So 4521-17-9 is a valid CAS Registry Number.

4521-17-9Downstream Products

4521-17-9Relevant academic research and scientific papers

Indium-Catalyzed Direct Conversion of Lactones into Thiolactones and Selenolactones in the Presence of Elemental Sulfur and Selenium

Sakai, Norio,Horikawa, Shuhei,Ogiwara, Yohei

, p. 565 - 574 (2017/12/26)

The direct conversion of lactones into thiolactones with elemental sulfur (S 8) catalyzed by InCl 3 /PhSiH 3 in a one-pot reaction is described. This catalytic system was successfully applied to the novel preparation of selenolactones from lactones and selenium.

Indium-catalyzed direct conversion of lactones into thiolactones using a disilathiane as a sulfur source

Ogiwara, Yohei,Takano, Ken,Horikawa, Shuhei,Sakai, Norio

, (2018/06/15)

An indium-catalyzed reaction of lactones and a disilathiane leading to thiolactones is described. The direct synthesis of thiolactones from lactones with an appropriate sulfur source is one of the most attractive approaches in organic and pharmaceutical chemistry. In this context, we found an indium-catalyzed direct conversion of lactones into thiolactones in the presence of elemental sulfur and a hydrosilane via formation of the disilathiane in situ. On the basis of the previous reaction, the application utilizing the disilathiane as a sulfur source was performed herein for the efficient synthesis of a variety of thiolactone derivatives from lactones by an indium catalyst.

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