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2(3H)-Thiophenone, dihydro-5-(4-methoxyphenyl)-, also known as 4-Methoxyphenyl-5,6-dihydro-2(3H)-thiophenone, is an organic compound with the molecular formula C11H12O2S. It is a derivative of thiophene, a heterocyclic compound consisting of a five-membered ring with one sulfur atom and four carbon atoms. In this specific compound, the thiophene ring is dihydrogenated, meaning it has two additional hydrogen atoms attached to the ring, and a 4-methoxyphenyl group is attached to the 5-position of the thiophene ring. The 4-methoxyphenyl group consists of a benzene ring with a methoxy group (-OCH3) attached to the 4-position. 2(3H)-Thiophenone, dihydro-5-(4-methoxyphenyl)- is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, and it exhibits potential applications in the development of new drugs and chemical compounds.

4521-27-1

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4521-27-1 Usage

Structural components

Thiophene ring, 4-methoxyphenyl group

Usage

Organic synthesis, building block for pharmaceuticals and agrochemicals

Potential applications

Medicine, agriculture, material science

Value

Therapeutic properties, versatile chemical in various industries

Check Digit Verification of cas no

The CAS Registry Mumber 4521-27-1 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, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4521-27:
(6*4)+(5*5)+(4*2)+(3*1)+(2*2)+(1*7)=71
71 % 10 = 1
So 4521-27-1 is a valid CAS Registry Number.

4521-27-1Downstream Products

4521-27-1Relevant academic research and scientific papers

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.

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.

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