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Carbamic acid, [3-(triethoxysilyl)propyl]-, 1-methylcyclohexyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

569352-47-2

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569352-47-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 569352-47-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,6,9,3,5 and 2 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 569352-47:
(8*5)+(7*6)+(6*9)+(5*3)+(4*5)+(3*2)+(2*4)+(1*7)=192
192 % 10 = 2
So 569352-47-2 is a valid CAS Registry Number.

569352-47-2SDS

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-methylcyclohexyl) N-(3-triethoxysilylpropyl)carbamate

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:569352-47-2 SDS

569352-47-2Downstream Products

569352-47-2Relevant academic research and scientific papers

Synthesis of acid-base bifunctional mesoporous materials by oxidation and thermolysis

Yu, Xiaofang,Zou, Yongcun,Wu, Shujie,Liu, Heng,Guan, Jingqi,Kan, Qiubin

, p. 951 - 957 (2011)

A novel and efficient method has been developed for the synthesis of acid-base bifunctional catalyst SO3H-MCM-41-NH2. This method was achieved by co-condensation of tetraethylorthosilicate (TEOS), 3-mercaptopropyltrimethoxysilane (MPTMS) and (3-triethoxysilylpropyl) carbamicacid-1-methylcyclohexylester (3TAME) in the presence of cetyltrimethylammonium bromide (CTAB), followed by oxidation and then thermolysis to generate acidic site and basic site. X-ray diffraction (XRD) and transmission electron micrographs (TEM) show that the resultant materials keep mesoporous structure. Thermogravimetric analysis (TGA), X-ray photoelectron spectra (XPS), back titration, solid-state 13C CP/MAS NMR and solid-state 29Si MAS NMR confirm that the organosiloxanes were condensed as a part of the silica framework. The bifunctional sample (SO 3H-MCM-41-NH2) containing amine and sulfonic acids exhibits excellent acid-basic properties, which make it possess high activity in aldol condensation reaction between acetone and various aldehydes.

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