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

89507-60-8

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89507-60-8 Usage

Molecular Weight

208.25 g/mol

Physical State

Colorless liquid

Uses

Reagent in organic synthesis, reactive diluent in epoxy resins, cross-linking agent in polymer chemistry, building block for pharmaceuticals and agrochemicals

Hazards

May cause skin and eye irritation, harmful if swallowed or inhaled.

Check Digit Verification of cas no

The CAS Registry Mumber 89507-60-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,5,0 and 7 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 89507-60:
(7*8)+(6*9)+(5*5)+(4*0)+(3*7)+(2*6)+(1*0)=168
168 % 10 = 8
So 89507-60-8 is a valid CAS Registry Number.

89507-60-8SDS

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-(2-methoxyethyl)phenoxy]methyl]oxirane

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:89507-60-8 SDS

89507-60-8Downstream Products

89507-60-8Relevant academic research and scientific papers

Synthesis method of metroprolol succinate ortho-isomer impurities

-

, (2020/03/06)

The invention belongs to the technical field of medicinal chemistry, and particularly relates to a synthesis method of metroprolol succinate ortho-isomer impurities. The synthesis method comprises thesteps: the metroprolol succinate ortho-isomer impurities are prepared by taking salicylaldehyde as a raw material through four steps of reactions, namely the Wittig reaction, the reduction hydrogenation reaction, the substitution reaction and the ring-opening reaction. The synthesis method of the metroprolol succinate ortho-isomer impurities totally includes the four steps of reactions, the raw material is easy to obtain, the total yield is greater than 40%, and contribution is made to strictly control the content of the metroprolol succinate ortho-isomer impurities through an external standard method; and the synthesis method of the metroprolol succinate ortho-isomer impurities is easy to operate, mild in reaction, high in product purity and suitable for drug quality study.

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