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2850-21-7

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2850-21-7 Usage

Description

2-[(4-Methoxyphenyl)sulfonyl]acetic acid ethyl ester is an organic compound that features a sulfonyl group attached to a phenyl ring, with a methoxy substituent at the para position. It also has an acetic acid ester functional group, which is connected to an ethyl group. This molecule is known for its reactivity and utility in the synthesis of various chemical compounds.

Uses

Used in Pharmaceutical Industry:
2-[(4-Methoxyphenyl)sulfonyl]acetic acid ethyl ester is used as a reactant for the preparation of (hetero)aryl alkyl sulfones, which are important intermediates in the synthesis of various pharmaceutical compounds. These sulfones can be further modified to develop new drugs with potential therapeutic applications.
Used in Chemical Synthesis:
In the field of chemical synthesis, 2-[(4-Methoxyphenyl)sulfonyl]acetic acid ethyl ester serves as a versatile building block for creating a wide range of organic molecules. Its reactivity in palladium-catalyzed reactions allows for the formation of complex molecular structures, which can be utilized in various applications, such as materials science, agrochemicals, and specialty chemicals.
Used in Research and Development:
2-[(4-Methoxyphenyl)sulfonyl]acetic acid ethyl ester is also used as a research compound in academic and industrial laboratories. It is valuable for exploring new reaction pathways, developing novel synthetic methods, and understanding the reactivity of sulfonyl-containing molecules. This knowledge can be applied to the design and synthesis of new molecules with specific properties and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 2850-21-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,5 and 0 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2850-21:
(6*2)+(5*8)+(4*5)+(3*0)+(2*2)+(1*1)=77
77 % 10 = 7
So 2850-21-7 is a valid CAS Registry Number.

2850-21-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-(4-methoxyphenyl)sulfonylacetate

1.2 Other means of identification

Product number -
Other names 6X-0941

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:2850-21-7 SDS

2850-21-7Relevant articles and documents

3-PHENYLSULPHONYL-QUINOLINE DERIVATIVES AS AGENTS FOR TREATING PATHOGENIC BLOOD VESSELS DISORDERS

-

, (2021/04/23)

The disclosure provides compounds, and compositions, including pharmaceutical compositions, kits that include the compounds, and methods of using (or administering) and making the compounds. The disclosure further provides compounds or compositions thereof for use in a method of modulating PLXDC1 (TEM7) and/or PLXDC2 or killing pathogenic blood vessles. The disclosure further provides compounds or compositions thereof for use in a method of treating a disease, disorder, or condition that is mediated, at least in part, by PEDF receptors or by angiogenesis.

Acenaphthoimidazolylidene Gold Complex-Catalyzed Alkylsulfonylation of Boronic Acids by Potassium Metabisulfite and Alkyl Halides: A Direct and Robust Protocol to Access Sulfones

Zhu, Haibo,Shen, Yajing,Deng, Qinyue,Chen, Jiangbo,Tu, Tao

, p. 4655 - 4659 (2017/07/24)

A robust acenaphthoimidazolylidene gold complex is demonstrated as a highly efficient catalyst in the direct alkylsulfonylation of boronic acids. Remarkably, a wide range of highly reactive and unreactive C-electrophiles were well-tolerated to produce various (hetero)aryl-alkyl, aryl-alkenyl, and alkenyl-alkyl sulfones in satisfactory yields with 5 mol % catalyst loading. Along with the steric properties of NHC ligands, the high catalytic activity of this gold complex suggests that the strong σ-donation of acenaphthoimidazolylidene also played a role in promoting this challenging redox-neutral catalytic process.

Bu4NI-Catalyzed Cross-Coupling between Sulfonyl Hydrazides and Diazo Compounds to Construct β-Carbonyl Sulfones Using Molecular Oxygen

Wang, Yaxiong,Ma, Liang,Ma, Meihua,Zheng, Hao,Shao, Ying,Wan, Xiaobing

supporting information, p. 5082 - 5085 (2016/10/14)

A new cross-coupling reaction between sulfonyl hydrazides and diazo compounds has been established, leading to a variety of β-carbonyl sulfones in good yields. This methodology was distinguished by simple manipulation, easily available starting materials, and wide substrate scope. A plausible mechanism involving a radical process was proposed based upon the experimental observations and literature.

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