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Urea, N,N''-(1S,2S)-1,2-cyclohexanediylbis[N'-[3-(triethoxysilyl)propyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

331850-59-0

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331850-59-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 331850-59-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,1,8,5 and 0 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 331850-59:
(8*3)+(7*3)+(6*1)+(5*8)+(4*5)+(3*0)+(2*5)+(1*9)=130
130 % 10 = 0
So 331850-59-0 is a valid CAS Registry Number.

331850-59-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3-triethoxysilylpropyl)-3-[(1S,2S)-2-(3-triethoxysilylpropylcarbamoylamino)cyclohexyl]urea

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:331850-59-0 SDS

331850-59-0Downstream Products

331850-59-0Relevant academic research and scientific papers

Shape-controlled bridged silsesquioxanes: Hollow tubes and spheres

Moreau, Joel J. E.,Vellutini, Luc,Chi Man, Michel Wong,Bied, Catherine

, p. 1594 - 1599 (2007/10/03)

A new approach for the morphological control of bridged silsesquioxanes has been achieved by the hydrolysis of silylated organic molecules bearing urea groups. The urea groups are responsible for the auto-association of the molecules through intermolecular hydrogen-bonding interactions. The self-assembly leads to supramolecular architectures that have the ability to direct the organization of hybrid silicas under controlled hydrolysis. The hydrolysis of the chiral diureido derivatives of trans-(1,2)-diaminocyclohexane 1 under basic conditions has been examined. The solid-state NMR spectra (29Si and 13C) showed the hybrid nature of these materials with wholly preserved Si-C covalent bonds throughout the silicate network. Hybrid silicas with hollow tubular morphologies were obtained by the hydrolysis of the enantiomerically pure compounds, (R,R)-1 or (S,S)-1, whereas the corresponding racemic mixture, rac-1, led to a hybrid with ball-like structures. The tubular shape is likely to result from a combination of two phenomena: the auto-association abilities and a self-templating structuration of the hybrid materials by the organic crystalline precursor. Electronic microscopy techniques (SEM and TEM) gave evidence for the self-templating pathway. The formation of the ball-like structures occurs through a usual nucleation growth phenomenon owing to a higher solubility of the corresponding crystals in the same medium.

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