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2211-94-1

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2211-94-1 Usage

Description

2,3-EPOXYPROPYL-4-METHOXYPHENYL ETHER, also known as Glycidyl 4-Methoxyphenyl Ether, is a white crystalline solid that is commonly utilized as a catalyst in various chemical reactions. Its unique chemical structure allows it to effectively initiate and control the polymerization process, making it a valuable compound in the field of polymer chemistry.

Uses

Used in Polymer Industry:
2,3-EPOXYPROPYL-4-METHOXYPHENYL ETHER is used as a catalyst for the radical polymerization of styrene. It plays a crucial role in the production of polystyrene and other styrene-based polymers, which are widely used in the manufacturing of plastics, rubber, and various other materials.
As a catalyst, 2,3-EPOXYPROPYL-4-METHOXYPHENYL ETHER helps to initiate the polymerization process by forming free radicals that react with styrene monomers. This reaction leads to the formation of a growing polymer chain, which eventually results in the formation of the desired polymer. The use of this catalyst allows for better control over the polymerization process, resulting in polymers with specific properties tailored to various applications.
In addition to its application in the polymer industry, 2,3-EPOXYPROPYL-4-METHOXYPHENYL ETHER may also find use in other industries where its unique chemical properties can be leveraged for specific purposes. However, based on the provided materials, the primary application of this compound is as a catalyst in the radical polymerization of styrene.

Check Digit Verification of cas no

The CAS Registry Mumber 2211-94-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,1 and 1 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2211-94:
(6*2)+(5*2)+(4*1)+(3*1)+(2*9)+(1*4)=51
51 % 10 = 1
So 2211-94-1 is a valid CAS Registry Number.

2211-94-1 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
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  • Detail
  • Alfa Aesar

  • (A19780)  Glycidyl 4-methoxyphenyl ether, 98%   

  • 2211-94-1

  • 5g

  • 560.0CNY

  • Detail
  • Alfa Aesar

  • (A19780)  Glycidyl 4-methoxyphenyl ether, 98%   

  • 2211-94-1

  • 25g

  • 1056.0CNY

  • Detail
  • Alfa Aesar

  • (A19780)  Glycidyl 4-methoxyphenyl ether, 98%   

  • 2211-94-1

  • 100g

  • 3076.0CNY

  • Detail
  • Aldrich

  • (148067)  Glycidyl4-methoxyphenylether  99%

  • 2211-94-1

  • 148067-25G

  • 2,088.45CNY

  • Detail

2211-94-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-2-[(4-methoxyphenoxy)methyl]oxirane

1.2 Other means of identification

Product number -
Other names 2,3-epoxypropyl para-methoxyphenyl ether

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:2211-94-1 SDS

2211-94-1Relevant articles and documents

β-Adrenergic antagonists with multiple pharmacophores: Persistent blockade of receptors

Pitha,Milecki,Czajkowska,Kusiak

, p. 7 - 11 (1983)

-

Substituted diaryl compound and preparation method and application thereof

-

Paragraph 0073-0075; 0076, (2021/09/15)

The invention relates to the field of medicinal chemistry, in particular to a substituted diaryl compound (I). The preparation method comprises the following steps: medicine preparation and medical application thereof. Test results show that the substituted diaryl compound has a good inhibition effect on human lung cancer (A549), human ovarian cancer (SKOV3), human melanoma (A375) and human colon cancer (LOVO) cells. Formula (I):

Engineering a homochiral metal-organic framework based on an amino acid for enantioselective separation

Tang, Haitong,Yang, Keke,Wang, Kun-Yu,Meng, Qi,Wu, Fan,Fang, Yu,Wu, Xiang,Li, Yougui,Zhang, WenCheng,Luo, Yunfei,Zhu, Chengfeng,Zhou, Hong-Cai

, p. 9016 - 9019 (2020/08/17)

A chiral metal-organic framework possessing an open amphiphilic channel is constructed from a dicarboxylate ligand derived from an amino acid and is shown to be an efficient and recyclable chiral solid adsorbent, which is capable of separating racemic secondary alcohols, epoxides, and ibuprofen with very high enantioselectivity.

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