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Phosphonic acid, [(2-methylphenyl)(methylthio)methyl]-, diethyl ester is a versatile chemical compound known for its diverse applications across various industries. It is characterized by its ability to act as a stabilizer for plastics and polymers, enhancing their durability and performance. Additionally, it serves as a catalyst in chemical reactions, facilitating the synthesis of various compounds. Its utility extends to the production of agrochemicals, pharmaceuticals, and organic synthesis, making it an essential component in the manufacturing and production processes of a wide range of products.

114100-03-7

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114100-03-7 Usage

Uses

Used in Plastics and Polymer Industry:
Phosphonic acid, [(2-methylphenyl)(methylthio)methyl]-, diethyl ester is used as a stabilizer for plastics and polymers to improve their durability and performance. Its incorporation into these materials helps prevent degradation and enhances their overall quality.
Used in Chemical Reactions:
In the field of chemistry, Phosphonic acid, [(2-methylphenyl)(methylthio)methyl]-, diethyl ester is employed as a catalyst to facilitate various chemical reactions. Its presence accelerates the reaction process, leading to more efficient and effective synthesis of desired compounds.
Used in Agrochemical Production:
Phosphonic acid, [(2-methylphenyl)(methylthio)methyl]-, diethyl ester is utilized in the production of agrochemicals, where it plays a crucial role in the development of effective and efficient products for agricultural applications. Its use contributes to the advancement of crop protection and enhancement strategies.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, Phosphonic acid, [(2-methylphenyl)(methylthio)methyl]-, diethyl ester is employed in the synthesis of various drugs and medicinal compounds. Its unique properties make it a valuable component in the development of novel pharmaceuticals with potential therapeutic benefits.
Used in Organic Synthesis:
Phosphonic acid, [(2-methylphenyl)(methylthio)methyl]-, diethyl ester is also used in organic synthesis, where it contributes to the creation of a wide range of organic compounds. Its versatility and reactivity make it an essential tool in the synthesis of various organic molecules for research and industrial applications.
It is important to handle Phosphonic acid, [(2-methylphenyl)(methylthio)methyl]-, diethyl ester with care and follow safety guidelines to ensure its safe and effective use in these applications.

Check Digit Verification of cas no

The CAS Registry Mumber 114100-03-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,1,0 and 0 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 114100-03:
(8*1)+(7*1)+(6*4)+(5*1)+(4*0)+(3*0)+(2*0)+(1*3)=47
47 % 10 = 7
So 114100-03-7 is a valid CAS Registry Number.

114100-03-7SDS

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-[diethoxyphosphoryl(methylsulfanyl)methyl]-2-methylbenzene

1.2 Other means of identification

Product number -
Other names -

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:114100-03-7 SDS

114100-03-7Downstream Products

114100-03-7Relevant academic research and scientific papers

Carbon-Carbon Bond Forming Reactions via α-Phosphoryl-α-thio Carbocations

Ishibashi, Hiroyuki,Sato, Tatsunori,Irie, Maki,Ito, Masae,Ikeda, Masazumi

, p. 1095 - 1098 (1987)

Diethyl chloro(methylthio)methylphosphonate (3) reacted with arenes and alk-1-enes in the presence of a Lewis acid to give the Friedel-Crafts product (5) and the ene product (8), respectively.The Pummerer rearrangement product (4) derived from diethyl (methylsulphinyl)methylphosphonate (10) also reacted with alk-1-enes in trifluoroacetic acid to give the products (8).

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