15251-78-2 Usage
Description
Methoxymethyl Phenyl Sulfone is a chemical compound that features a sulfonyl group and a methoxymethyl substituent attached to a phenyl ring. It is widely recognized for its utility as a building block in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. This versatile compound also serves as an intermediate in the manufacture of dyes and pigments, and it has shown promise as an effective UV-protective agent, making it a candidate for use in sunscreen formulations. Furthermore, Methoxymethyl Phenyl Sulfone plays a significant role in material science and polymer chemistry, where it contributes to the development of polymers with specific properties for a range of industrial applications.
Uses
Used in Pharmaceutical and Agrochemical Production:
Methoxymethyl Phenyl Sulfone is used as a key building block in the synthesis of various pharmaceuticals and agrochemicals. Its unique structure allows for the creation of a wide range of compounds with different therapeutic and pesticidal properties.
Used in Dye and Pigment Manufacturing:
Methoxymethyl Phenyl Sulfone is utilized as an intermediate in the production of dyes and pigments, contributing to the development of colorants with specific characteristics for use in various industries.
Used in Sunscreen Formulations:
Methoxymethyl Phenyl Sulfone is used as a potential UV-protective agent in sunscreen formulations. Its effectiveness in protecting against harmful UV rays is currently being researched, indicating its potential use in cosmetic and personal care products.
Used in Material Science and Polymer Chemistry:
Methoxymethyl Phenyl Sulfone is used as a versatile material in material science and polymer chemistry. It aids in the development of polymers with tailored properties, suitable for a variety of industrial applications, including coatings, adhesives, and plastics.
Check Digit Verification of cas no
The CAS Registry Mumber 15251-78-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,2,5 and 1 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 15251-78:
(7*1)+(6*5)+(5*2)+(4*5)+(3*1)+(2*7)+(1*8)=92
92 % 10 = 2
So 15251-78-2 is a valid CAS Registry Number.
15251-78-2Relevant articles and documents
Enantioselective Aromatic Sulfide Oxidation and Tandem Kinetic Resolution Using Aqueous H2O2 and Chiral Iron–Bis(oxazolinyl)bipyridine Catalysts
Jalba, Angela,Régnier, Noémie,Ollevier, Thierry
, p. 1628 - 1637 (2017/04/06)
An efficient method for the oxidation of aromatic sulfides has been developed by using aqueous H2O2, catalyzed by the in situ generated chiral Fe/6,6′-bis(4-isopropyloxazolin-2-yl)-2,2′-bipyridine (bipybox-iPr) complex. The corresponding sulfoxides were obtained with high enantioselectivities (up to 98.5:1.5 er) and in good yields (up to 61 %) when the mono-oxidation of the sulfides was performed in combination with the kinetic resolution of the sulfoxide into the sulfone.
Chromium(VI) oxide catalyzed oxidation of sulfides to sulfones with periodic acid
Xu, Liang,Cheng, Jie,Trudell, Mark L.
, p. 5388 - 5391 (2007/10/03)
A highly efficient and selective oxidation of sulfides to sulfones with periodic acid catalyzed by CrO3 is described. A variety of electron-rich and electron-deficient sulfides were oxidized to sulfones with 2 mol% CrO3 in acetonitrile at room temperature in excellent yields. Sulfides with other readily oxidized functional groups were selectively oxidized to sulfones in high yields with 10 mol% CrO3 in ethyl acetate/acetonitrile at -35 °C.
Ketone homologation to produce α-methoxyketones: Application to conduritol synthesis
Phillipson, Neil,Anson, Michael S.,Montana, John G.,Taylor, Richard J. K.
, p. 2821 - 2829 (2007/10/03)
The scope of Trost's sulfone homologation procedure for the conversion of ketones into their α-methoxylated higher homologues has been dramatically expanded. The use of zirconium (or hafnium) tetrachloride in the hydroxy sulfone rearrangement step gives g
