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1-(3-chlorophenylthio)propan-2-one is an organic compound with the molecular formula C9H9ClOS. It is a derivative of propan-2-one, featuring a 3-chlorophenylthio group attached to the carbon atom at position 1. This chemical is characterized by its unique structure, which includes a ketone functional group, a sulfur atom, and a chlorine atom. It is a colorless to pale yellow solid and is used in the synthesis of various pharmaceuticals and agrochemicals due to its reactivity and versatility. The compound's properties, such as its melting point, solubility, and stability, can be influenced by the presence of the chlorine atom and the sulfur-containing group, making it a valuable intermediate in organic chemistry.

40806-13-1

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40806-13-1 Usage

Chemical structure

1-(3-chlorophenylthio)propan-2-one consists of a thioether group attached to a propan-2-one backbone, and a chlorine atom attached to the benzene ring.

Usage

Commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals.

Reactivity

Has the potential to act as a reactive intermediate in organic chemical reactions, especially in the formation of carbon-carbon and carbon-sulfur bonds.

Applications

Its unique structure and reactivity make it a valuable building block for the production of various organic compounds with diverse applications.

Safety concerns

It is important to handle this chemical with care, as it may pose health and safety risks due to its potential for skin and eye irritation, as well as its flammability.

Check Digit Verification of cas no

The CAS Registry Mumber 40806-13-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,8,0 and 6 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 40806-13:
(7*4)+(6*0)+(5*8)+(4*0)+(3*6)+(2*1)+(1*3)=91
91 % 10 = 1
So 40806-13-1 is a valid CAS Registry Number.

40806-13-1Downstream Products

40806-13-1Relevant academic research and scientific papers

α-Arylchalcogenation of acetone with diaryl dichalcogenide via metal-free oxidative C(sp3)-H bond functionalization

Yan, Guobing,Borah, Arun Jyoti,Wang, Lianggui,Pan, Zhangjin,Chen, Shuangshuang,Shen, Xuqian,Wu, Xiangmei

, p. 4305 - 4307 (2015)

Direct α-arylchalcogenation of acetone with diaryl dichalcogenides has been achieved by using a mixture of TBHP and DTBP oxidants at 120 °C without transition-metal catalyst via oxidative C(sp3)-H bond functionalization. The method exhibits good functional group tolerance and products were isolated in moderate to high yields.

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