15620-78-7 Usage
Description
2-[(2-ethylphenoxy)methyl]oxirane, also known as ethylphenylglycidyl ether, is a chemical compound with the molecular formula C11H14O2. It is a clear, colorless liquid at room temperature and exhibits low volatility. 2-[(2-ethylphenoxy)methyl]oxirane possesses an epoxide functional group, making it useful for a wide range of applications in the production of adhesives, coatings, and composites.
Uses
Used in Adhesives Industry:
2-[(2-ethylphenoxy)methyl]oxirane is used as a reactive diluent in epoxy resins for improving the flow and curing properties of adhesive formulations.
Used in Coatings Industry:
2-[(2-ethylphenoxy)methyl]oxirane is used as a reactive diluent in epoxy resins for enhancing the performance and durability of coatings.
Used in Composites Industry:
2-[(2-ethylphenoxy)methyl]oxirane is used as a reactive diluent in epoxy resins for improving the mechanical properties and processability of composite materials.
Used in Organic Synthesis:
2-[(2-ethylphenoxy)methyl]oxirane is used as a building block for the synthesis of various organic compounds due to its epoxide functional group.
Note: Exposure to high levels of 2-[(2-ethylphenoxy)methyl]oxirane can be harmful, causing irritation to the skin, eyes, and respiratory system, and may have potential mutagenic and carcinogenic effects. Therefore, proper safety measures should be taken when handling this chemical.
Check Digit Verification of cas no
The CAS Registry Mumber 15620-78-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,6,2 and 0 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 15620-78:
(7*1)+(6*5)+(5*6)+(4*2)+(3*0)+(2*7)+(1*8)=97
97 % 10 = 7
So 15620-78-7 is a valid CAS Registry Number.
15620-78-7Relevant articles and documents
Synthesis of all of the stereoisomers of β3-adrenoceptor antagonist SR 59230 based on the spontaneous resolution of 3-(2-ethylphenoxy)propane-1,2-diol
Bredikhina, Zemfira A.,Kurenkov, Alexey V.,Krivolapov, Dmitry B.,Bredikhin, Alexander A.
, p. 467 - 474 (2016/06/06)
Racemic 3-(2-ethylphenoxy)propane-1,2-diol 2 has been effectively resolved into (S)- and (R)-enantiomers by a preferential crystallization procedure. Non-racemic diols 2, obtained via a Mitsunobu reaction, have been converted into the non-racemic 1,2-epox
Antihypertensive indole derivatives of phenoxypropanolamines with β-adrenergic receptor antagonist and vasodilating activity
Kreighbaum,Matier,Dennis,Minielli,Deitchman,Perhach Jr.,Comer
, p. 285 - 289 (2007/10/02)
A series of 25 aryloxypropanolamines containing the 3-indolyl-tert-butyl[i.e., 1,1-dimethyl-2-(1H-indol-3-yl)ethyl] or substituted 3-indolyl-tert-butyl moiety as the N substituent is reported. These compounds have been tested for antihypertensive activity in spontaneously hypertensive rats (SHR), β-adrenergic receptor antagonist action in conscious normotensive rats, vasodilating activity in ganglion-blocked rats with blood pressure maintained by angiotensin II infusion, and for intrinsic sympathomimetic action (ISA) in reserpinized rats. Some of the compounds exhibit antihypertensive activity in combination with β-adrenergic receptor antagonist and vasodilating action. The structure-activity relationships in these tests are discussed.
