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3-Methylphenoxathiine is a chemical compound with the molecular formula C9H9OS2. It is a derivative of phenoxathiin, which is a heterocyclic organic compound containing sulfur and oxygen atoms. 3-methylphenoxathiine is characterized by the presence of a methyl group (-CH3) attached to the phenyl ring, which contributes to its unique chemical properties. 3-Methylphenoxathiine is known for its potential applications in various fields, such as pharmaceuticals and agrochemicals, due to its ability to act as a precursor for the synthesis of other compounds. It is also recognized for its potential use as a pesticide or insecticide, although further research is needed to fully understand its efficacy and safety. The compound's structure and reactivity make it an interesting subject for study in organic chemistry and related fields.

46412-20-8

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46412-20-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 46412-20-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,6,4,1 and 2 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 46412-20:
(7*4)+(6*6)+(5*4)+(4*1)+(3*2)+(2*2)+(1*0)=98
98 % 10 = 8
So 46412-20-8 is a valid CAS Registry Number.

46412-20-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methylphenoxathiine

1.2 Other means of identification

Product number -
Other names 3-Methyl-phenoxathiine

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:46412-20-8 SDS

46412-20-8Downstream Products

46412-20-8Relevant academic research and scientific papers

Efficient Synthesis of Phenoxathiines via the Cascade C–H Hydroxylation–C–S Coupling–C–O Cyclization Reaction

Chao, Fei,Xu, Wen-Heng,Ren, Zhi-Lin,Wang, Long

, p. 2558 - 2561 (2019)

The ligand-free and simple cascade C–H hydroxylation–C–S coupling–C–O cyclization reaction has been used as the synthetic approach to disulfides and o-chloro-iodobenzenes using CuI as a catalyst. This approach provides an easy and convenient method of synthesis of phenoxathiin derivatives.

Synthesis of phenoxathiins and phenothiazines by aryne reactions with thiosulfonates

Hosoya, Takamitsu,Kanemoto, Kazuya,Sakata, Yuki,Yoshida, Suguru

, p. 593 - 596 (2020/05/19)

Novel synthetic methods for phenoxathiins and phenothiazines by aryne reactions are disclosed. We found that phenoxathiins were efficiently prepared by the reaction between aryne intermediates and S-(2-hydroxyaryl) 4-toluenethiosulfo-nates. A synthetic method for phenothiazines was also developed by the reaction of arynes with S-(2-aminoaryl) 4-toluenethiosulfonates.

Regioselective synthesis of phenoxathiin derivatives under transition-metal-free conditions

Hu, Fangdong,Zhao, Xin,Li, Yanqiu,Feng, Lei,Ma, Chen

, p. 966 - 970 (2013/05/09)

A simple and efficient method was developed for the synthesis of phenoxathiin derivatives. A range of 1,2-dihaloarenes or 1-halo-2-nitroarenes reacted with 2-sulfanylphenol to give the desired products in good-to-excellent yields. It is intriguing that 1-halo-2-nitroarenes containing electron-donating groups worked well as substrates in this reaction. Georg Thieme Verlag Stuttgart - New York.

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