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  • 2388-74-1 Structure
  • Basic information

    1. Product Name: 3-METHOXY THIOANISOLE
    2. Synonyms: 3-METHOXY THIOANISOLE;3-METHOXY THIOANISOLE 99%MIN;(3-methoxyphenyl)(methyl)sulfane;1-(Methylthio)-3-methoxybenzene;1-Methoxy-3-(methylthio)benzene;1-Methylthio-3-methoxybenzene;Methyl (3-methoxyphenyl) sulfide;Methyl [3-(methylthio)phenyl] ether
    3. CAS NO:2388-74-1
    4. Molecular Formula: C8H10OS
    5. Molecular Weight: 154.23
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 2388-74-1.mol
    9. Article Data: 20
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 127 °C / 18mmHg
    3. Flash Point: 93 °C
    4. Appearance: /
    5. Density: 1.12
    6. Refractive Index: 1.5820 to 1.5860
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3-METHOXY THIOANISOLE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-METHOXY THIOANISOLE(2388-74-1)
    11. EPA Substance Registry System: 3-METHOXY THIOANISOLE(2388-74-1)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT, STENCH
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 2388-74-1(Hazardous Substances Data)

2388-74-1 Usage

Description

3-Methoxy Thioanisole, an organosulfur and phenolic chemical compound, is known for its distinct odor and clear, colorless liquid appearance. It is soluble in various organic solvents and is widely used in manufacturing and research as a reagent in organic synthesis. However, due to its potential hazards, such as causing skin irritation and serious eye damage, it is essential to handle 3-Methoxy Thioanisole with care and wear appropriate protective gear.

Uses

Used in Chemical Synthesis:
3-Methoxy Thioanisole is used as a reagent in organic synthesis for its organosulfur and phenolic properties. It plays a crucial role in the production of various chemical compounds and intermediates, contributing to the advancement of the chemical industry.
Used in Manufacturing:
In the manufacturing industry, 3-Methoxy Thioanisole is utilized in the production of various products, including pharmaceuticals, agrochemicals, and other specialty chemicals. Its unique properties make it a valuable component in the synthesis of complex molecules and compounds.
Used in Research:
3-Methoxy Thioanisole is also employed in research settings, where it serves as a valuable tool for studying the properties and reactions of organosulfur and phenolic compounds. Researchers use it to explore new chemical pathways, develop innovative synthetic methods, and gain insights into the behavior of similar compounds.
Safety Precautions:
When handling 3-Methoxy Thioanisole, it is crucial to take necessary safety precautions to minimize potential hazards. Protective gear, such as gloves and eye protection, should be worn to prevent skin irritation and serious eye damage. Additionally, proper storage and disposal methods should be followed to ensure the safe handling of this chemical compound.

Check Digit Verification of cas no

The CAS Registry Mumber 2388-74-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,8 and 8 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2388-74:
(6*2)+(5*3)+(4*8)+(3*8)+(2*7)+(1*4)=101
101 % 10 = 1
So 2388-74-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H10O2S/c1-9-7-4-3-5-8(6-7)11-10-2/h3-6H,1-2H3

2388-74-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methoxy-3-methylsulfanylbenzene

1.2 Other means of identification

Product number -
Other names 3-(Methylthio)anisole

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:2388-74-1 SDS

2388-74-1Relevant articles and documents

Pd-Catalyzed Intermolecular Transthiolation of Ar-OTf Using Methyl 3-(Methylthio) Propanoate as a Thiol Surrogate

Pan, Dandan,Xu, Shasha,Tian, Qingqiang,Li, Yahui

supporting information, p. 4616 - 4619 (2021/09/10)

A method for the odorless synthesis of unsymmetrical sulfides via Csp2?O and Csp3?S bond activation is presented. Using methyl 3-(methylthio) propanoate as a MeSH surrogate, a series of substituted aryl methyl sulfides have been obtained in moderate to good yields. This catalytic protocol can also tolerate methyl 3-(methylthio)propionate derivatives to afford the corresponding aryl sulfides.

FORMIMIDAMIDINE COMPOUNDS USEFUL AGAINST PHYTOPATHOGENIC MICROORGANISMS

-

Page/Page column 68, (2018/12/12)

The present invention relates to 4-substituted amidine derivatives of the general formula (I), wherein A1-A4, D, L, Q, R7, R7' and integer's v and w have the meanings as defined in description. The invention further relates to methods for their preparation and use of said compounds to fight undesired phytopathogenic microorganisms, and agents for said purpose, comprising said amidine derivatives, all according to the invention. This invention further relates to a method for controlling undesired phytopathogenic microorganisms by application of said 4-substituted amidine derivatives of general formula (I) to such undesired microorganisms and/or to their habitat, according to the invention. (I)

N-Imidazolylation of Sulfoximines from N-Cyano Sulfoximines, 1-Alkynes, and N-Sulfonyl Azides

Kim, Sanghyuck,Kim, Ji Eun,Lee, Jinsub,Lee, Phil Ho

supporting information, p. 3707 - 3717 (2016/01/25)

The rhodium-catalyzed N-imidazolylation of N-sulfonyl-1,2,3-triazoles with a variety of N-cyano sulfoximines has been developed for the synthesis of N-imidazolyl sulfoximines via elimination of molecular nitrogen. Copper-catalyzed [3+2] cycloaddition followed by rhodium-catalyzed N-imidazolylation from 1-alkynes, N-sulfonyl azides, and N-cyano sulfoximines is also demonstrated for the synthesis of N-imidazolyl sulfoximines in a one-pot procedure.

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