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1,3,5-tris(phthalimidomethyl)-2,4,6-triethylbenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

828931-45-9

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828931-45-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 828931-45-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,2,8,9,3 and 1 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 828931-45:
(8*8)+(7*2)+(6*8)+(5*9)+(4*3)+(3*1)+(2*4)+(1*5)=199
199 % 10 = 9
So 828931-45-9 is a valid CAS Registry Number.

828931-45-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3,5-tris(phthalimidomethyl)-2,4,6-triethylbenzene

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:828931-45-9 SDS

828931-45-9Relevant academic research and scientific papers

Compounds Combining a Macrocyclic Building Block and Flexible Side-Arms as Carbohydrate Receptors: Syntheses and Structure-Binding Activity Relationship Studies

Amrhein, Felix,Mazik, Monika

, p. 6282 - 6303 (2021)

A series of new representatives of compounds combining a macrocyclic building block and flexible side-arms were prepared and their ability to act as carbohydrate receptors evaluated. The target compounds were obtained by multi-step syntheses, which included the preparation of numerous precursors as well as the isolation of a large number of by-products. The structure-binding activity relationship studies comprise, in particular, the variation of the side-arms in order to demonstrate the importance of the presence of a hydrogen bond donor in these units for the effective complexation of carbohydrates. Based on the findings of our previous studies, the variation of the bridge units is limited to benzene- and pyrrole-based moieties, whereby the use of the last-mentioned bridge type was expected to produce more effective systems. This assumption was confirmed by 1H NMR titrations and isothermal titration calorimetry.

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