26163-11-1 Usage
Description
2,6-DIMETHOXYBENZENETHIOL, with the molecular formula C9H12O2S, is a white solid chemical compound characterized by a strong, unpleasant odor. It is primarily utilized in the synthesis of various organic compounds and serves as a reagent in the preparation of thioether derivatives. 2,6-DIMETHOXYBENZENETHIOL also exhibits potential as a corrosion inhibitor and has shown promise in medicinal chemistry due to its biological activities, which may contribute to drug development.
Uses
Used in Organic Synthesis:
2,6-DIMETHOXYBENZENETHIOL is used as a key intermediate in the synthesis of various organic compounds, playing a crucial role in the development of new chemical entities and materials.
Used as a Reagent in Thioether Derivatives Preparation:
In the field of organic chemistry, 2,6-DIMETHOXYBENZENETHIOL serves as a reagent for the preparation of thioether derivatives, which are important in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used as a Corrosion Inhibitor:
2,6-DIMETHOXYBENZENETHIOL has demonstrated its potential as a corrosion inhibitor, making it a valuable component in formulations for protecting metals from corrosion in various industrial applications.
Used in Medicinal Chemistry:
In the pharmaceutical industry, 2,6-DIMETHOXYBENZENETHIOL is used for its biological activities, which may contribute to the development of new drugs and therapeutic agents.
It is important to handle 2,6-DIMETHOXYBENZENETHIOL with care, as it can be harmful if swallowed, inhaled, or in contact with skin.
Check Digit Verification of cas no
The CAS Registry Mumber 26163-11-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,1,6 and 3 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 26163-11:
(7*2)+(6*6)+(5*1)+(4*6)+(3*3)+(2*1)+(1*1)=91
91 % 10 = 1
So 26163-11-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H10O2S/c1-9-6-4-3-5-7(10-2)8(6)11/h3-5,11H,1-2H3
26163-11-1Relevant articles and documents
Alkyl sulfinates: Formal nucleophiles for synthesizing TosMIC analogs
Lujan-Montelongo, J. Armando,Estevez, Angel Ojeda,Fleming, Fraser F.
supporting information, p. 1602 - 1605 (2015/03/04)
Alkyl sulfinates function as formal nucleophiles in Mannich-type reactions to give sulfonyl formamides, which are readily dehydrated to the corresponding sulfonylmethyl isonitriles. The efficient, two-step synthesis provides a general route to sulfonylmethyl isonitriles from readily available methyl sulfinates or thiols. Mechanistic analysis reveals that the unusual nucleophlicity of the alkyl sulfinates arises from the in situ release of sulfinic acids.
Trimethoxyphenylthio as a highly labile replacement for tert-butylthio cysteine protection in fmoc solid phase synthesis
Postma, Tobias M.,Albericio, Fernando,Giraud, Matthieu
supporting information, p. 5468 - 5471,4 (2012/12/13)
Trimethoxyphenylthio (S-Tmp) is described as a novel cysteine protecting group in Fmoc solid phase peptide synthesis replacing the difficult to remove tert-butylthio. S-Tmp and dimethoxyphenylthio (S-Dmp) were successfully used for cysteine protection in a variety of peptides. Moreover, both groups can be removed in 5 min with mild reducing agents. S-Tmp is recommended for cysteine protection, as it yields crude peptides of high purity.
Bis(2,6-dimethoxyphenyl) sulfide, selenide and telluride, and their derivatives
Wada, Masanori,Nobuki, Shin-Ichi,Tenkyuu, Yoshinori,Natsume, Satoko,Asahara, Masahiro,Erabi, Tatsuo
, p. 282 - 289 (2007/10/03)
2,6-Dimethoxyphenyl derivatives of sulfur, selenium, and tellurium, such as ΦEEΦ, Φ2E, ΦSeH, [MeΦ2E]X (X = MeSO4, ClO4), Φ2EO · xH2O, [Φ2EOH]ClO4, [Φ2EOR]Cl
