81055-36-9

Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule of the compound.

Explanation

Describes the arrangement of atoms and functional groups within the molecule.

Explanation

Indicates that the compound is artificially synthesized and consists of carbon, hydrogen, and other elements.

Explanation

Highlights the compound's role in chemical reactions, specifically in creating new bonds between carbon atoms.

Explanation

Indicates that the compound serves as a starting material for the synthesis of other significant compounds.

Explanation

Emphasizes the compound's importance in the manufacturing of a wide range of products within the chemical sector.

Structure

Propane backbone with a bromine atom at the first carbon and a toluene-4-sulfonyloxy group at the third carbon

Type of compound

Synthetic organic compound

Applications

Used as a reagent in organic synthesis, particularly in the formation of carbon-carbon bonds

Utilization

Preparation of pharmaceuticals, agrochemicals, and other fine chemicals

Role

Precursor to other important chemical compounds

Value

Production of various products in the chemical industry

Upstream product

• 824-79-3 sodium 4-methylbenzenesulfinate 
• 627-18-9 1-bromo-3-propanol 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 92357-95-4 10-(3-bromopropyl)phenothiazine 
• 74252-85-0 1-(benzylsulfanyl)-3-(p-toluenesulfonyloxy)propane 
• 108607-98-3 1-bromo-3-[¹⁸F]fluoropropane 
• 113426-14-5 3-[18F]fluoropropyl p-tosylate 
• 24308-28-9 1,3-propanesultine 

Relevant academic research and scientific papers

IONIC LIQUID, LUBRICANT, AND MAGNETIC RECORDING MEDIUM

To provide an ionic liquid or the like which is excellent in thermal stability, solubility in a fluorine-based solvent, and fluidity, has a high bonding ratio, and is capable of forming a thin monomolecular film.SOLUTION: The ionic liquid comprises a cati

Rapid transformation of sulfinate salts into sulfonates promoted by a hypervalent iodine(III) reagent

An alternative method for forming sulfonates through hypervalent iodine(III) reagent-mediated oxidation of sodium sulfinates has been developed. This transformation involves trapping reactive sulfonium species using alcohols. With additional optimization of the reaction conditions, the method appears extendable to other nucleophiles such as electron-rich aromatic systems or cyclic ethers through a ring opening pathway.

PROCESS OF PREPARING A RADIOACTIVE COMPOUND CONTAINING A FLUORINE-18 ISOTOPE

A process of preparing a radioactive compound containing a fluorine-18 isotope is provided. In one embodiment, the process may comprise forming a [18F] fluoroalkyl triflate by triflating a [18F] fluoroalkyl compound with AgOTf, and f

Stereocontrolled synthesis of novel enantiomerically pure sulfides and selenides from (+)-camphor and (+)-camphor-10-sulfonyl chloride

Synthetic approaches to novel enantiomerically pure sulfides and selenides derived from (+)-camphor and (+)-camphor-10-sulfonate esters are described. Lewis acid mediated hemiacetal formation between a camphor- derived ketone and a thiol or selenol, and subsequent in situ reduction using triethylsilane selectively gives the exo-sulfide or -selenide in moderate overall yields. The initial sulfonate ester products can be converted into the corresponding sulfones by subsequent treatment with Grignard or organolithium reagents.