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50605-34-0

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50605-34-0 Usage

Type of compound

Epoxide compound (contains a three-membered ring consisting of one oxygen atom and two carbon atoms)

Common uses

Crosslinker in the production of epoxy resins (used in adhesives, coatings, and composites), Reactive diluent in epoxy formulations (improved processing characteristics and better control of viscosity)

Properties

Low volatility, high reactivity, excellent adhesion.

Check Digit Verification of cas no

The CAS Registry Mumber 50605-34-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,6,0 and 5 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 50605-34:
(7*5)+(6*0)+(5*6)+(4*0)+(3*5)+(2*3)+(1*4)=90
90 % 10 = 0
So 50605-34-0 is a valid CAS Registry Number.
InChI:InChI=1/C14H20O2/c1-4-14(2,3)11-5-7-12(8-6-11)15-9-13-10-16-13/h5-8,13H,4,9-10H2,1-3H3

50605-34-0SDS

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-methylbutan-2-yl)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:50605-34-0 SDS

50605-34-0Downstream Products

50605-34-0Relevant articles and documents

SUBSTITUTED DIHYDRO AND TETRAHYDRO OXAZOLOPYRIMIDINONES, PREPARATION AND USE THEREOF

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Page/Page column 37, (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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