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112968-90-8

112968-90-8

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112968-90-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112968-90-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,9,6 and 8 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 112968-90:
(8*1)+(7*1)+(6*2)+(5*9)+(4*6)+(3*8)+(2*9)+(1*0)=138
138 % 10 = 8
So 112968-90-8 is a valid CAS Registry Number.

112968-90-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[2-(2-methoxyethoxy)ethoxy]-4-prop-2-enylbenzene

1.2 Other means of identification

Product number -
Other names Benzene,1-[2-(2-methoxyethoxy)ethoxy]-4-(2-propenyl)

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:112968-90-8 SDS

112968-90-8Downstream Products

112968-90-8Relevant articles and documents

Comparison of Oligo(ethylene oxide)-Substituted Posysiloxanes with Poly(ethylene glycol) as Stationary Phases for Capillary Chromatography

Rouse, Christine A.,Finlinson, Ann C.,Tarbet, Bryon J.,Pixton, Jennifer C.,Djordjevic, Nebojsa M.,et al.

, p. 901 - 905 (2007/10/02)

The gas chromatographic properties of a new oligo(ethylene oxide)-substituted (glyme) polysiloxane stationary phase and an 18-crown-6-substituted (crown) polysiloxane phase were compared to Carbowax 20M and a bonded poly(ethylene glycol) (Bondable PEG).The glyme polysiloxane was found to have an operational temperature range of 20-280 deg C and a selectivity similar to that of Carbowax 20M.The crown polysiloxane was found to have unique selectivity, partly because of the size and shape of the crown ether cavity and the structures of solute molecules.Selected applications including the analysis of alcohols, fused oils, and nitrogen heterocycles are demonstrated.

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