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5877-11-2

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5877-11-2 Usage

Description

[(2-chloropropyl)sulfanyl]benzene, with the molecular formula C9H11ClS, is a chemical compound that exists as a clear, colorless liquid at room temperature and has a strong odor. It is utilized as an intermediate in the synthesis of other organic compounds and serves as a solvent in various industrial processes. Due to its potential harmful effects when inhaled, ingested, or in contact with skin, it is crucial to handle and store this chemical with care, using proper personal protective equipment and ensuring a well-ventilated area.

Uses

Used in Chemical Synthesis:
[(2-chloropropyl)sulfanyl]benzene is used as an intermediate in the chemical synthesis of other organic compounds. Its unique structure allows for further reactions and the creation of a variety of products, contributing to the versatility of this compound in the chemical industry.
Used in Industrial Solvents:
[(2-chloropropyl)sulfanyl]benzene is also employed as a solvent in various industrial processes. Its ability to dissolve a range of substances makes it a valuable asset in the production of different materials and products.
Used in Pharmaceutical Industry:
[(2-chloropropyl)sulfanyl]benzene can be used as a building block for the development of pharmaceutical compounds. Its reactivity and structural properties make it a suitable candidate for the synthesis of new drugs with potential therapeutic applications.
Used in Research and Development:
Due to its unique chemical properties, [(2-chloropropyl)sulfanyl]benzene is also utilized in research and development settings. Scientists and researchers can use this compound to study various chemical reactions and explore its potential applications in creating new materials or improving existing ones.

Check Digit Verification of cas no

The CAS Registry Mumber 5877-11-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,7 and 7 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5877-11:
(6*5)+(5*8)+(4*7)+(3*7)+(2*1)+(1*1)=122
122 % 10 = 2
So 5877-11-2 is a valid CAS Registry Number.

5877-11-2Relevant articles and documents

SUBSTITUTED NICOTINAMIDES AS KCNQ2/3 MODULATORS

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Page/Page column 20, (2010/09/18)

The invention relates to substituted nicotinamides, to processes for their preparation, to medicaments comprising these compounds and to the use of these compounds in the preparation of medicaments.

REACTION OF SULFENYL HALIDES WITH ALKENES IN THE PRESENCE OF PERCHLORIC ACID

Grudzinskaya, E. Yu.,Skorobogatova, E. V.

, p. 1710 - 1713 (2007/10/02)

In the reaction of 2,4-dinitrobenzenesulfenyl chloride and benzenesulfenyl chloride with cyclohexane, propene, and styrene in acetic acid in the presence of perchloric acid the corresponding solvent adducts are formed with yields of 47-75percent.The effect of the perchloric acid on the rate of the reaction of 2,4-dinitrobenzenesulfenyl chloride with cyclohexene is described by an equation for homogeneous catalysis.On the basis of the kinetic data two possible schemes are proposed for the effect of perchloric acid on the formation of the solvent adducts, i.e., a mechanism of homogeneous catalysis and by an ion-exchange mechanism in the noncontrolling stages of the reaction.

ALKENE CARBOSULPHENYLATION AND CARBOSELENYLATION: THE USE OF ALLYLTRIMETHYLSILANE AND O-SILYLATED ENOLATES.

Alexander, Rikki P.,Paterson, Ian

, p. 5911 - 5914 (2007/10/02)

Allyltrimethylsilane, as well as O-silylated enolates, can be alkylated by the PhSCl adducts of alkenes and vinyl ethers (1, X=SPh); the PhSeCl analogues (1, X=SePh), however, are less useful for alkylation purposes due to competing nucleophilic attack at selenium.

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