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Benzene, 1-methoxy-2-(methylsulfinyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

38452-13-0

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38452-13-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38452-13-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,4,5 and 2 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 38452-13:
(7*3)+(6*8)+(5*4)+(4*5)+(3*2)+(2*1)+(1*3)=120
120 % 10 = 0
So 38452-13-0 is a valid CAS Registry Number.

38452-13-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methoxy-2-methylsulfinylbenzene

1.2 Other means of identification

Product number -
Other names 1-methylsulfinyl-2-methoxybenzene

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:38452-13-0 SDS

38452-13-0Relevant academic research and scientific papers

Hypervalent iodine(III) oxidation catalyzed by quaternary ammonium salt in miceliar systems

Tohma, Hirofumi,Takizawa, Shinobu,Watanabe, Hiroaki,Kita, Yasuyuki

, p. 4547 - 4550 (1998)

Catalytic activation of iodosobenzene (PhI=O) by cetyltrimethylammonium bromide (CTAB) allows sulfide oxidation reaction to occur in high yields under mild conditions in a variety of solvents. This PhI=O activation may be due to the formation of micellar

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.

Extending aromatic acids on TiO2 for cooperative photocatalysis with triethylamine: Violet light-induced selective aerobic oxidation of sulfides

Lang, Xianjun,Li, Hui,Li, Xia,Sheng, Wenlong,Zhou, Jun

supporting information, (2022/01/11)

Designing visible light photocatalysts with a metal oxide semiconductor as the starting material could expand a new horizon for the conversion and storage of solar energy. Here, the benchmark photocatalyst TiO2 was used to pursue this goal by a

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.

Sulfoxide and Sulfone Synthesis via Electrochemical Oxidation of Sulfides

Lee, Sunwoo,Park, Jin Kyu

, p. 13790 - 13799 (2021/10/12)

The oxidation of diaryl sulfides and aryl alkyl sulfides to the corresponding sulfoxides and sulfones under electrochemical conditions is reported. Sulfoxides are selectively obtained in good yield under a constant current of 5 mA for 10 h in DMF, while sulfones are formed as the major product under a constant current of 10 or 20 mA for 10 h in MeOH. The oxygen of both the sulfoxide and sulfone function is derived from water.

Bridging green light photocatalysis over hierarchical Nb2O5for the selective aerobic oxidation of sulfides

Ma, Xiaoming,Hao, Huimin,Sheng, Wenlong,Huang, Fengwei,Lang, Xianjun

supporting information, p. 2214 - 2222 (2021/02/09)

Nb2O5is a colourless metal oxide that is very promising in areas such as energy storage and optical glasses. These applications depend on the superior redox properties of Nb2O5compared to those of other metal ox

Air atmospheric photocatalytic oxidation by ultrathin C,N-TiO2nanosheets

Cheng, Xiuyan,Zhang, Jianling,Liu, Lifei,Zheng, Lirong,Zhang, Fanyu,Duan, Ran,Sha, Yufei,Su, Zhuizhui,Xie, Fei

supporting information, p. 1165 - 1170 (2021/02/26)

Herein, we demonstrate the highly efficient photocatalytic sulfide oxidation reaction under mild conditions,i.e.in air, at room temperature and in the absence of a sacrificial reagent, co-catalyst or redox mediator, by using ultrathin C,N-TiO2nanosheets as a photocatalyst.

Two-dimensional crystalline covalent triazine frameworksviadual modulator control for efficient photocatalytic oxidation of sulfides

Jin, Shangbin,Lang, Xianjun,Li, Xia,Tan, Bien,Wang, Xuepeng,Zhan, Zhen,Zhang, Siquan

supporting information, p. 16405 - 16410 (2021/08/09)

Two-dimensional crystalline covalent triazine frameworks (2D-CTFs) are emerging 2D materials with the characteristics of fully annulated conjugated structures and aromatic nitrogen-rich skeletons. Due to the difficulty in the control of the polymerization

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