Welcome to LookChem.com Sign In|Join Free

CAS

  • or

1074-02-8

Post Buying Request

1074-02-8 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

1074-02-8 Usage

General Description

2-(Methylsulfinyl)benzenol, also known as methyleugenol, is a naturally occurring compound found in certain essential oils and herbs. It is commonly used as a flavoring agent in the food and beverage industry due to its sweet, spicy, and slightly clove-like aroma. Methyleugenol is also used in the fragrance industry as a scent ingredient, as well as in traditional medicine for its potential therapeutic properties. However, it has been identified as a potential carcinogen and genotoxic compound, raising some concerns about its safety and use in consumer products. As a result, regulations and restrictions on the use of methyleugenol in food and cosmetic products have been implemented in various countries to minimize potential health risks.

Check Digit Verification of cas no

The CAS Registry Mumber 1074-02-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,7 and 4 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1074-02:
(6*1)+(5*0)+(4*7)+(3*4)+(2*0)+(1*2)=48
48 % 10 = 8
So 1074-02-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H8O2S/c1-10(9)7-5-3-2-4-6(7)8/h2-5,8H,1H3

1074-02-8SDS

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 2-(Methylsulfinyl)phenol

1.2 Other means of identification

Product number -
Other names 2-methylsulfinylphenol

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:1074-02-8 SDS

1074-02-8Relevant articles and documents

ON THE DEMONSTRATION OF OPTICALLY ACTIVE HYDROXYPHENYLALKYL-SULFOXIDES.

WAGNER,BOEHME

, p. 257 - 272 (1964)

-

Oxygenation of Organoboronic Acids by a Nonheme Iron(II) Complex: Mimicking Boronic Acid Monooxygenase Activity

Chatterjee, Sayanti,Paine, Tapan Kanti

supporting information, p. 9727 - 9732 (2015/11/03)

Phenolic compounds are important intermediates in the bacterial biodegradation of aromatic compounds in the soil. An Arthrobacter sp. strain has been shown to exhibit boronic acid monooxygenase activity through the conversion of different substituted phenylboronic acids to the corresponding phenols using dioxygen. While a number of methods have been reported to cleave the C-B bonds of organoboronic acids, there is no report on biomimetic iron complex exhibiting this activity using dioxygen as the oxidant. In that direction, we have investigated the reactivity of a nucleophilic iron-oxygen oxidant, generated upon oxidative decarboxylation of an iron(II)-benzilate complex [(TpPh2)FeII(benzilate)] (TpPh2 = hydrotris(3,5-diphenyl-pyrazol-1-yl)borate), toward organoboronic acids. The oxidant converts different aryl/alkylboronic acids to the corresponding oxygenated products with the incorporation of one oxygen atom from dioxygen. This method represents an efficient protocol for the oxygenation of boronic acids with dioxygen as the terminal oxidant.

Synthetic routes to polyheteroacenes: Characterization of a heterocyclic ladder polymer containing phenoxathiinium-type building blocks

Oyaizu, Kenichi,Mikami, Takefumi,Mitsuhashi, Fumio,Tsuchida, Eishun

, p. 67 - 78 (2007/10/03)

The synthetic routes to ladder polymers that consist of benzenetetrayl subunits with oxo and methylsulfonio linkages are described. As the key intermediate, poly(phenylene oxide)s having pendant methylsulfenyl groups are prepared by copper-catalyzed oxidative polymerization of the corresponding phenols with O2. The oxidation of the polymer with an equimolar amount of H2O2 in the presence of acetic acid effects the high-yielding conversion of methylsulfenyl to methylsulfinyl groups without the formation of the undesired methylsulfonyl groups. The superacidified condensation of the resulting polymer (Swern reaction of aryl sulfoxides) under dilution conditions induces the polymer-analogous intramolecular electrophilic ring-closing reaction of the hydroxymethylphenylsulfonium cation onto the adjacent benzene ring to yield the required ladder polymer, which has proved to be a semiconductor with an intrinsic electric conductivity of 2 × 10-5 S/cm. A comparison of the spectroscopic properties of the ladder polymer with those of the model compounds such as 5-methylphenoxathiinium triflate and phenoxathiin discloses π-electron delocalization over the methylsulfonio linkages, demonstrating the efficacy of the ladderization for p-π/d-π interactions in arylsulfonium moieties. This synthetic approach permits the thio and alkylsulfonio ladder linkages for a variety of phenyl ethers to form in high yields.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 1074-02-8