26910-41-8 Usage
Description
[(2-chloropropan-2-yl)sulfinyl]benzene, also known as 2-Propylsulfinylphenyl chloride, is a chemical compound belonging to the phenyl chlorides family, characterized by the presence of a chlorine atom attached to a benzene ring. With the molecular formula C9H11ClOS, this compound is a sulfoxide, featuring a sulfur atom bonded to two organic groups. Its chemical properties and reactivity contribute to its utility in various applications, particularly in the synthesis of pharmaceuticals, agrochemicals, and as a building block in organic chemistry.
Uses
Used in Pharmaceutical Synthesis:
[(2-chloropropan-2-yl)sulfinyl]benzene is used as an intermediate in the pharmaceutical industry for the development of new drugs. Its unique chemical structure allows for the creation of a wide range of therapeutic compounds, making it a valuable asset in drug discovery and design.
Used in Agrochemical Production:
In the agrochemical industry, [(2-chloropropan-2-yl)sulfinyl]benzene is utilized as a key component in the synthesis of various pesticides and other agricultural chemicals. Its incorporation into these products helps improve their effectiveness in protecting crops and controlling pests.
Used as a Building Block in Organic Chemistry:
[(2-chloropropan-2-yl)sulfinyl]benzene serves as a versatile building block in organic chemistry, enabling the synthesis of a diverse array of organic compounds. Its reactivity and structural features make it an attractive candidate for use in the development of novel materials and chemical products.
Safety Precautions:
Given the potential hazards associated with [(2-chloropropan-2-yl)sulfinyl]benzene, it is crucial to handle this chemical with care and follow proper safety protocols. This includes using appropriate personal protective equipment, ensuring proper ventilation, and adhering to established guidelines for storage and disposal.
Check Digit Verification of cas no
The CAS Registry Mumber 26910-41-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,9,1 and 0 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 26910-41:
(7*2)+(6*6)+(5*9)+(4*1)+(3*0)+(2*4)+(1*1)=108
108 % 10 = 8
So 26910-41-8 is a valid CAS Registry Number.
26910-41-8Relevant articles and documents
Synthesis and allergenic potential of a 15-hydroperoxyabietic acid-like model: Trapping of radical intermediates
Mutterer,Gimenez Arnau,Karlberg,Lepoittevin
, p. 1028 - 1036 (2007/10/03)
To better understand the skin sensitization mechanism of 15-hydroperoxyabietic acid-like compounds, 2-(1'-hydroperoxy-1'-methylethyl)-4a-methyl-3,4,4a,5,6,7-hexahydronaphthalene 7 was synthesized. The allergenic activity of this compound was tested on mice using the local lymph node assay, and further evaluated on guinea pigs using the Freund's complete adjuvant test. Using these methods, hydroperoxide 7 was found to be a strong sensitizer. Radical-trapping experiments were carried out on this compound in the presence of the spin-trapping agent, 1,1,3,3-tetramethylisoindolin-2-yloxyl 17, using light to induce radicals. The formation of carbon-centered radicals derived from compound 7 by intramolecular cyclization of an oxygen-centered radical was observed. The reaction of these intermediates with 17 gave various adducts in a very low yield, but a 1/1 mixture of diastereomers 18a and 18b (0.1% yield) was isolated and characterized, together with compound 19 (0.03% yield). The results suggest that carbon-centered reactive radicals are formed from allylic hydroperoxides and that this could be the possible mechanism involved in allergic contact dermatitis to abietic acid.
