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146669-14-9

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146669-14-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 146669-14-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,6,6 and 9 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 146669-14:
(8*1)+(7*4)+(6*6)+(5*6)+(4*6)+(3*9)+(2*1)+(1*4)=159
159 % 10 = 9
So 146669-14-9 is a valid CAS Registry Number.

146669-14-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-N,3-N,5-N-tris(2-aminoethyl)benzene-1,3,5-tricarboxamide

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:146669-14-9 SDS

146669-14-9Relevant articles and documents

Synthesis of new liquid phase carriers for use in large scale oligonucleotide synthesis in solution

Woerl, Ralf,Koester, Hubert

, p. 2941 - 2956 (1999)

The synthesis of multifunctional symmetric primary amines 4 and 8 and the covalent binding of 5'-O-dimethoxytrityl-deoxynucleoside derivatives to their amino groups (compound 5 and 9) is described. Different strategies for dedimethoxytritylation including the use of strong acidic ion exchangers or protic acids and modified silica gels and/or gel permeation chromatography are developed. The resulting liquid phase carriers 6 and 10 are suitable for large scale oligonucleotide synthesis in solution using phosphoamidites and gel permeation chromatography for fast isolation of intermediates.

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.

Supramolecular compounds from multiple ugi multicomponent macrocyclizations: Peptoid-based cryptands, cages, and cryptophanes

Rivera, Daniel G.,Wessjohann, Ludger A.

, p. 7122 - 7123 (2007/10/03)

The first 3-fold multicomponent macrocyclizations of trifunctional building blocks were developed to produce, in one pot, cryptands, cages, and cryptophanes with peptoid tethers carrying additional recognition motifs. The straightforward, efficient, and d

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