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61578-04-9

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61578-04-9 Usage

Reactivity Profile

[[4-(1-methyl-1-phenylethyl)phenoxy]methyl]-oxiran is an ether. Ethers may react violently with strong oxidizing agents. In other reactions, which typically involve the breaking of the carbon-oxygen bond, ethers are relatively inert.

Fire Hazard

Flash point data for [[4-(1-methyl-1-phenylethyl)phenoxy]methyl]-oxiran are not available. [[4-(1-methyl-1-phenylethyl)phenoxy]methyl]-oxiran is probably combustible.

Check Digit Verification of cas no

The CAS Registry Mumber 61578-04-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,5,7 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 61578-04:
(7*6)+(6*1)+(5*5)+(4*7)+(3*8)+(2*0)+(1*4)=129
129 % 10 = 9
So 61578-04-9 is a valid CAS Registry Number.

61578-04-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[[4-(2-phenylpropan-2-yl)phenoxy]methyl]oxirane

1.2 Other means of identification

Product number -
Other names 4-(1-Methyl-1-phenylethyl)-phenyl glycidyl 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:61578-04-9 SDS

61578-04-9Upstream product

61578-04-9Downstream Products

61578-04-9Relevant articles and documents

SUBSTITUTED DIHYDRO AND TETRAHYDRO OXAZOLOPYRIMIDINONES, PREPARATION AND USE THEREOF

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Page/Page column 39, (2010/04/23)

The present invention relates to a series of substituted dihydro and tetrahydro oxazolopyrimidinones, specifically, to a series of 2-substituted-2,3-dihydro-oxazolo[3,2-a]pyrimidin-7-ones and 2-substituted-2,3,5,6-tetra-hydro-oxazolo[3,2-a]pyrimidin-7-ones of formula (I): Wherein p, n, X, Y, R1, R2, R3, R4, R5, R6, R7 and R8 are as defined herein. This invention also relates to methods of making these compounds including novel intermediates. The compounds of this invention are modulators of metabotropic glutamate receptors (mGluR), particularly, mGluR2 receptor. Therefore, the compounds of this invention are useful as pharmaceutical agents, especially in the treatment and/or prevention of a variety of central nervous system disorders (CNS), including but not limited to acute and chronic neurodegenerative conditions, psychoses, convulsions, anxiety, depression, migraine, pain, sleep disorders and emesis.

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