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Phosphonic acid, [1-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)ethyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

59191-43-4

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59191-43-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59191-43-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,1,9 and 1 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 59191-43:
(7*5)+(6*9)+(5*1)+(4*9)+(3*1)+(2*4)+(1*3)=144
144 % 10 = 4
So 59191-43-4 is a valid CAS Registry Number.

59191-43-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(1,3-dioxoisoindol-2-yl)ethylphosphonic acid

1.2 Other means of identification

Product number -
Other names Phosphonic acid,[1-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)ethyl]

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:59191-43-4 SDS

59191-43-4Relevant academic research and scientific papers

Inhibitory effect of synthetic aminophosphonic acid derivatives on human carbonic anhydrase

Oesapay, G,Csiba, A

, p. 355 - 361 (1993)

A series of phosphonic analogs of amino acids, peptides, and their derivatives was synthesized in order to examine their ability to inhibit human carbonic anhydrase (HCA) isoenzymes (I and II).The aminophosphonic acids with amino protection possess much stronger inhibitory capacity (Ki = 10-6 - 10-5 M) than the free aminophosphonic acids (Ki = 10-5 - 10-3 M).The aminophosphonic acids with both N- and P-protection do not have an inhibitory effect on the esterase activity of HCA.In a comparison of the enantiomeric pairs of Cbz-AlaP(OH)2, the D-conformer has several-fold stronger inhibitory potency.All aminoalkylphosphonates investigated possess one order of magnitude stronger inhibitory activity towards isoenzyme HCA-I than towards HCA-II.A computer-directed analysis was used to study the possible interactions in an aminoalkylphosphonate P(OH)2>-(HCA-II) complex. aminophosphonic acid / human carbonic anhydrase / esterase activity inhibition / computer modelling

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