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1-Methoxy-2-(Methylsulfonyl)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13736-79-3

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13736-79-3 Usage

Structure

A chemical compound consisting of a methoxy group (-OCH3) and a methylsulfonyl group (-SO2CH3) attached to a benzene ring.

Usage

Commonly used as a fragrance ingredient in perfumes and personal care products.

Odor

Possesses a sweet, floral, and slightly fruity odor.

Biological activities

Studied for its potential antimicrobial and anti-inflammatory properties.

Industrial application

Used as an intermediate in the production of other organic compounds and pharmaceuticals.

Stability

Considered to be relatively stable and non-reactive under normal conditions.

Versatility

Due to its stability and various properties, 1-Methoxy-2-(Methylsulfonyl)benzene is a useful chemical in different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 13736-79-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,7,3 and 6 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 13736-79:
(7*1)+(6*3)+(5*7)+(4*3)+(3*6)+(2*7)+(1*9)=113
113 % 10 = 3
So 13736-79-3 is a valid CAS Registry Number.

13736-79-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methoxy-2-methylsulfonylbenzene

1.2 Other means of identification

Product number -
Other names 1-methoxy-2-(methylsulfonyl)benzene

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:13736-79-3 SDS

13736-79-3Relevant academic research and scientific papers

Hydrophilic phase transfer catalyst based on the sulfoacid group and polyoxometalate for the selective oxidation of sulfides in water with hydrogen peroxide

Zhao, Wei,Yang, Chunxia,Liu, Kecheng,Yang, Ying,Chang, Tao

, p. 447 - 451 (2017)

A hybrid catalyst, based on SO3H-fuctionalized quaternary ammonium and polyoxovanadometalate, was synthesized and used for the selective oxidation of sulfides in water at room temperature. The highest turnover numbers (TON) can reach up to 1536. The organic products with high yields can be easily separated and the catalytic system can be used several times with the retention of catalytic activity.

Highly Crystalline Ag-based Coordination Polymers for Efficient Photocatalytic Oxidation of Sulfides

Cheng, Xiuyan,Jin, Yigang,Li, Yang,Li, Ze,Liu, Liyao,Sun, Yimeng,Xu, Wei,Zhang, Jianling,Zou, Ye

supporting information, (2022/03/15)

Coordination polymers (CPs) display great potential for the development of highly active photocatalysts. Herein, we report the fabrication of a highly crystalline CP, [Ag2BTT]n (BTT=benzene-1,2,4,5-tetrathiol). The crystal structure of [Ag2BTT]n was resolved and its performance for photocatalytic oxidation of thioanisole was explored. [Ag2BTT]n is highly active and selective for the photo-oxidation of sulfides to sulfoxides under mild conditions, that is, in air, at room temperature and in the absence of a sacrificial reagent, co-catalyst or redox mediator.

High Chemoselectivity in the Construction of Aryl Methyl Sulfones via an Unexpected C-S Bond Formation between Sulfonylhydrazides and Dimethyl Phosphite

Liu, Teng,Yu, Shiwen,Shen, Xiang,Li, Yixian,Liu, Jianjun,Huang, Chao,Cheng, Feixiang

, p. 153 - 160 (2021/10/04)

A highly chemoselective route to aryl methyl sulfones via an unexpected C S bond formation between sulfonylhydrazides and dimethyl phosphite catalyzed by NaI under mild conditions has been established. This transformation provides an alternative and metal-free pathway to acquire various aryl methyl sulfones in good to excellent yields. Notably, dimethyl phosphite was employed as a stable and readily available alkyl source.

A μ-AsO4-Bridging Hexadecanuclear Ni-Substituted Polyoxotungstate

Lian, Chen,Li, Hai-Lou,Yang, Guo-Yu

, p. 3996 - 4003 (2021/04/07)

A novel tetrahedral μ-AsO4-bridging hexadecanuclear Ni-substituted silicotungstate (ST) Na21H10[(AsO4){Ni8(OH)6(H2O)2(CO3)2(A-α-SiW9O34)2}2]·60H2O (1) was made by the reactions of trivacant [A-α-SiW9O34]10- ({SiW9}) units with Ni2+ cations and Na3AsO4·12H2O and characterized by IR spectrometry, elemental analysis, thermogravimetric analysis (TGA), and powder X-ray diffraction (PXRD). 1 contains a novel polyoxoanion [(AsO4){Ni8(OH)6(H2O)2(CO3)2(A-α-SiW9O34)2}2]31- built by four trivacant Keggin [A-α-SiW9O34]10- fragments linked through an unprecedented [(AsO4){Ni8(OH)6(H2O)2(CO3)2}2]9+ cluster, where the tetrahedral AsO4 acts as an exclusively μ2-bridging unit to link multiple Ni centers; such a connection mode appears for the first time in polyoxometalate chemistry. Furthermore, the electrochemical and catalytic oxidation properties of compound 1 have been investigated.

A {Ti6W4}-Cluster-Substituted Polyoxotungstate: Synthesis, Structure, and Catalytic Oxidation Properties

Li, Hai-Lou,Lian, Chen,Yang, Guo-Yu

supporting information, p. 14622 - 14628 (2021/10/01)

A novel Ti-W-O-cluster-substituted tungstoantimonate (TA), [H2N(CH3)2]3Na4H9[{Ti6W4O18(OH)(H2O)3}(B-α-SbW9O33)3]·20H2O (1), has been made by hydrothermal reactions of trivacant [B-α-SbW9O33]9- units, Ti4+ cations, and WO42- anions in the presence of [H2N(CH3)2]·Cl and structurally characterized. Intriguingly, the polyoxoanion of 1 is constructed from three [B-α-SbW9O33]9- units and a previously unobserved decanuclear heterometallic Ti-W-O cluster [Ti6W4O18(OH)(H2O)3]11+ ({Ti6W4}) that is comprised of an octahedral [Ti6WO6(H2O)3]18+ cluster and an edge-sharing [W3O12(OH)]7- fragment via six W-O-Ti/W linkers. Furthermore, studies on the catalytic oxidation properties reveal that 1 possesses good catalytic activity toward the oxidation reactions of various sulfides and cyclooctene based on the environmentally friendly oxidant H2O2.

{Ti6}/{Ti10} Wheel Cluster Substituted Silicotungstate Aggregates

Li, Hai-Lou,Lian, Chen,Yang, Guo-Yu

, p. 16852 - 16859 (2021/11/13)

Two novel Ti-oxo wheel cluster substituted silicotungstates (STs) [H2N(CH3)2]9H9[Ti6O6(SiW10O37)3]·11H2O (1) and [H2N(CH3)2]16H10[Ti10O11(SiW10O37)2(SiW9O35)2]·14H2O (2) have been made by hydrothermal reactions. The polyoxoanion of 1 is a ring-shaped trimer where a Ti6O6 ({Ti6}) wheel cluster is encapsulated by three divacant [SiW10O37]10- (SiW10O37) fragments. However, 2 is built by two divacant SiW10O37 units and two rare trivacant [SiW9O35]12- (SiW9O35) fragments and further installs an unprecedented Ti10O11 ({Ti10}) double-wheel cluster. To the best of our knowledge, 2 is rare in POM chemistry. Studies on the catalytic oxidation properties reveal that 1 exhibits high catalytic activity toward the oxidation of various sulfides using H2O2 as an oxidant. Furthermore, 1 can be facilely recycled and reused for at least five cycles without obvious loss of catalytic activity.

Preparation method of methyl sulfone compound

-

Paragraph 0005; 0026, (2021/02/24)

The invention discloses a synthesis method of a methyl sulfone compound, which comprises the following steps: by using an iodinated compound as a substrate, adding a sulfite compound into the substrate, and using a 1, 4-dioxane solution as a solvent, heating under the protection of nitrogen under the actions of a silicon reagent, a phase transfer catalyst and a palladium catalyst to obtain a crudeproduct; then purifying the crude product, firstly filtering the crude product, and removing the solvent to obtain residues; carrying out silica gel column chromatography on the residues, leaching with eluent, and collecting effluent; combining the effluent containing the product; and concentrating the combined effluent to remove the solvent, and finally carrying out vacuum drying to obtain the target product. The method has the advantages of simple process flow, easiness in product purification, environmental safety and high yield.

PI4KIIIBETA INHIBITORS

-

Page/Page column 65, (2019/08/08)

The invention relates to compounds of formula (I) which are inhibitors of kinase activity, pharmaceutical formulations containing the compounds and their uses in treating and preventing viral infections and disorders caused or exacerbated by the viral inf

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.

Green Organocatalytic Oxidation of Sulfides to Sulfoxides and Sulfones

Voutyritsa, Errika,Triandafillidi, Ierasia,Kokotos, Christoforos G.

, p. 917 - 924 (2017/02/15)

A highly efficient synthetic methodology towards the selective synthesis of sulfoxides and sulfones is reported using a cheap and green organocatalytic method. Starting from sulfides and using 2,2,2-trifluoroacetophenone as the organocatalyst and H2O2 as the oxidant, the high-yielding preparation of sulfoxides or sulfones is described, being dependent on the reaction conditions.

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