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3-phenyl-benzo[c]thiophen-1(3H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

42495-97-6

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42495-97-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 42495-97-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,4,9 and 5 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 42495-97:
(7*4)+(6*2)+(5*4)+(4*9)+(3*5)+(2*9)+(1*7)=136
136 % 10 = 6
So 42495-97-6 is a valid CAS Registry Number.

42495-97-6Downstream Products

42495-97-6Relevant 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.

Synthesis of N-substituted (Z)-3-arylbenzo[c]thiophen1(3H)-imines by the reaction of 1-[aryl(methoxy)methyl]2-lithiobenzenes with isothiocyanates followed by acid-mediated cyclization

Kobayashi, Kazuhiro,Shigemura, Yuuho,Ezaki, Kosuke

, p. 526 - 536 (2015/08/10)

A simple procedure for the preparation of N-substituted (Z)-3-arylbenzo [c]thiophen-1(3H)-imines has been developed. Thus, bromine/lithium exchange between 1-[aryl(methoxy)methyl]-2-bromobenzenes and butyllithium, followed by reaction of the resulting 1-[

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