24165-03-5 Usage
Description
TRIPHENYLMETHANESULFENYL CHLORIDE, also known as Trityl Chloride, is an aromatic organic compound characterized by its yellow solid appearance. It is a triphenylmethane derivative with a chlorine atom attached to the sulfur atom. TRIPHENYLMETHANESULFENYL CHLORIDE is known for its reactivity and is widely utilized in various chemical processes due to its unique properties.
Uses
Used in Chemical Synthesis:
TRIPHENYLMETHANESULFENYL CHLORIDE is used as an intermediate in the preparation of precursors for cyclic polysulfides. Its reactivity and stability make it a valuable component in the synthesis of these complex molecules, which have potential applications in various industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, TRIPHENYLMETHANESULFENYL CHLORIDE is used as a reagent for the synthesis of various drugs and drug candidates. Its unique chemical properties allow it to participate in a range of reactions, contributing to the development of new and improved medications.
Used in Research and Development:
TRIPHENYLMETHANESULFENYL CHLORIDE is also employed in research and development settings, where it is used to study the properties and behavior of various chemical compounds. Its reactivity and stability make it an ideal tool for exploring new reaction pathways and understanding the mechanisms behind complex chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 24165-03-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,1,6 and 5 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 24165-03:
(7*2)+(6*4)+(5*1)+(4*6)+(3*5)+(2*0)+(1*3)=85
85 % 10 = 5
So 24165-03-5 is a valid CAS Registry Number.
InChI:InChI=1/C19H15ClS/c20-21-19(16-10-4-1-5-11-16,17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-15H
24165-03-5Relevant articles and documents
Ciuffarin,Guaraldi
, p. 1745 (1969)
Catalytic asymmetric Pictet-Spengler reactions via sulfenyliminium ions
Wanner, Martin J.,Van Der Haas, Richard N. S.,De Cuba, Kimberly R.,Van Maarseveen, Jan H.,Hiemstra, Henk
, p. 7485 - 7487 (2008/09/17)
(Chemical Equation Presented) From cations to chiral products: β-Carbo-lines can be synthesized with good enantioselectivity by the title reaction catalyzed by a chiral binol-derived Bronsted acid (see scheme, BHT = 3,5-di(tert-butyl)-4-hydroxytoluene). T
The Synthesis of Substituted thio>acetic Acids
Woulfe, Steven R.,Miller, Marvin J.
, p. 3133 - 3139 (2007/10/02)
The synthesis of substituted thio>acetic acids (6, thiamazins) is described.Various substituted 3(S)-(acylamino)-2-azetidinones were sulfenylated with tert-butyl (phtalimidothio)acetate.Deprotection of the tert-butyl ester with trifluoroacetic acid provided the title compounds.In sharp contrast to their oxygen analogues (oxamazins), the thiamazins were devoid of biological activity.