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819883-45-9

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819883-45-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 819883-45-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,1,9,8,8 and 3 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 819883-45:
(8*8)+(7*1)+(6*9)+(5*8)+(4*8)+(3*3)+(2*4)+(1*5)=219
219 % 10 = 9
So 819883-45-9 is a valid CAS Registry Number.

819883-45-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-N,3-N-bis(3-aminopropyl)benzene-1,3-dicarboxamide

1.2 Other means of identification

Product number -
Other names bis-propylamineisophthalamide

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:819883-45-9 SDS

819883-45-9Downstream Products

819883-45-9Relevant articles and documents

Bisphosphonate sequestering agents. Synthesis and preliminary evaluation for in vitro and in vivo uranium(VI) chelation

Sawicki, Marcin,Lecercle, Delphine,Grillon, Gerard,Le Gall, Beatrice,Serandour, Anne-Laure,Poncy, Jean-Luc,Bailly, Theodorine,Burgada, Ramon,Lecouvey, Marc,Challeix, Vincent,Leydier, Antoine,Pellet-Rostaing, Stephane,Ansoborlo, Eric,Taran, Frederic

experimental part, p. 2768 - 2777 (2009/04/06)

A library of bisphosphonate-based ligands was prepared using solution-phase parallel synthesis and tested for its uranium-binding properties. With the help of a screening method, based on a chromophoric complex displacement procedure, 23 dipodal and tripodal chelates bearing bisphosphonate chelating functions were found to display very high affinity for the uranyl ion and were selected for evaluation of their in vivo uranyl-removal efficacy. Among them, 11 ligands induced a huge modification of the uranyl biodistribution by deviating the metal from kidney and bones to liver. Among the other ligands, the most potent was the dipodal bisphosphonate 3C which reduced the retention of uranyl and increased its excretion by around 10% of the injected metal.

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