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16543-43-4

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16543-43-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16543-43-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,5,4 and 3 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 16543-43:
(7*1)+(6*6)+(5*5)+(4*4)+(3*3)+(2*4)+(1*3)=104
104 % 10 = 4
So 16543-43-4 is a valid CAS Registry Number.

16543-43-4SDS

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 isopropylphenylphosphonic acid

1.2 Other means of identification

Product number -
Other names isopropyl-phenyl-phosphinic acid

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:16543-43-4 SDS

16543-43-4Relevant articles and documents

A Chromogenic Crown Ether as a Sensing Molecule in Optical Sensors for the Detection of Hard Metal Ions

Gent, Jos van,Sudhoelter, Ernst J. R.,Lambeck, Paul V.,Popma, Theo J. A.,Gerritsma, Gerrit J.,Reinhoudt, David N.

, p. 893 - 895 (1988)

A new chromogenic crown ether based on a merocyanine dye and a phenolic crown ether shows a striking selectivity for calcium or barium complexation and has a potential use in optical sensors.

Dramatic influence of the nature of the surfactant aggregate on the rate constant for hydrolysis of phosphinate esters in aqueous nematic lyotropic liquid crystals

Ramesh,Labes

, p. 738 - 741 (2007/10/02)

The o-iodosobenzoic acid catalyzed hydrolysis of two organophosphinate esters has been studied in the lyotropic nematic phases of myrystyltrimethylammonium bromide in 1-decanol, ammonium bromide, and water. Depending on the concentration of these ingredients, three phases are observed at room temperature consisting of rod-like (N//C), disk-like (N//L), or sphere-like (I) aggregates. There is a three order of magnitude difference in the rate constant for hydrolysis between N//L and N//C phases. The N//L phase serves as a protective environment, preventing the hydrolysis of the ester, whereas the N//C phase allows the reaction to occur rapidly. Based upon infrared evidence, the phosphinate ester is solubilized in the hydrocarbon region of N//L aggregates, but in N// C and I aggregates the solute is nearer the aqueous interface.

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