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5296-35-5

2-[(2-ethoxyphenoxy)methyl]oxirane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 5296-35-5 Structure

  • Basic information

    1. Product Name: 2-[(2-ethoxyphenoxy)methyl]oxirane
    2. Synonyms: 2-[(2-ethoxyphenoxy)methyl]oxirane;1-(2-Ethoxyphenoxy)-2,3-epoxypropane;2-Ethoxyphenyl Glycidyl Ether
    3. CAS NO:5296-35-5
    4. Molecular Formula: C11H14O3
    5. Molecular Weight: 194.22706
    6. EINECS: N/A
    7. Product Categories: Aromatics;Intermediates
    8. Mol File: 5296-35-5.mol

  • Chemical Properties

    1. Melting Point: 45 °C
    2. Boiling Point: 122 °C(Press: 4 Torr)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.114±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: Refrigerator
    8. Solubility: Dichloromethane, Ethyl Acetate
    9. CAS DataBase Reference: 2-[(2-ethoxyphenoxy)methyl]oxirane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-[(2-ethoxyphenoxy)methyl]oxirane(5296-35-5)
    11. EPA Substance Registry System: 2-[(2-ethoxyphenoxy)methyl]oxirane(5296-35-5)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 5296-35-5(Hazardous Substances Data)

5296-35-5 Usage

Chemical Properties

Colourless Oil

Uses

Intermediate in the preparation of Morpholine derivatives.

Check Digit Verification of cas no

The CAS Registry Mumber 5296-35-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,9 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5296-35:
(6*5)+(5*2)+(4*9)+(3*6)+(2*3)+(1*5)=105
105 % 10 = 5
So 5296-35-5 is a valid CAS Registry Number.

5296-35-5SDS

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 2-(2-Ethoxyphenoxymethyl)oxirane

1.2 Other means of identification

Product number -
Other names 2-[(2-Ethoxyphenoxy)methyl]oxirane

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:5296-35-5 SDS

5296-35-5Relevant articles and documents

Substituted diaryl compound and preparation method and application thereof

-

Paragraph 0073-0075, (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):

Design, synthesis and biological evaluation of novel desloratadine derivatives with anti-inflammatory and H1 antagonize activities

Li, Feng,Xu, Qinlong,Zhu, Qihua,Chu, Zhaoxing,Lin, Gaofeng,Mo, Jiajia,Zhao, Yan,Li, Jiaming,He, Guangwei,Xu, Yungen

, (2019/11/03)

To improve the anti-inflammatory activity of desloratadine, we designed and synthesized a series of novel desloratadine derivatives. All compounds were evaluated for their anti-inflammatory and H1 antagonistic activities. Among them, compound 2c showed the strongest H1 antagonistic and anti-inflammatory activity. It also exhibited promising pharmacokinetic profiles and low toxicity. All these results suggest that compound 2c as a novel anti-allergic agent is worthy of further investigation.

METHODS FOR PRODUCING VILOXAZINE SALTS AND NOVEL POLYMORPHS THEREOF

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Page/Page column 11, (2011/10/19)

Provided here are methods of manufacture of viloxazine and its various salts, as well as viloxazine-related compounds, such as novel intermediate reaction products and polymorphs thereof. In particular, the methods provide a substantially pure API of viloxazine HCl while avoiding undesirable impurities. The methods further provide for separating, identifying, and characterizing novel polymorphs of viloxazine. Further provided are methods for synthesis and identification and characterization of novel intermediates of viloxazine, as well as for some important metabolites and precursors of metabolites of viloxazine.

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