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1223-16-1

1223-16-1

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  • BIS(P-AMINOPHENOXY)DIMETHYLSILANE CAS NO.1223-16-1 CAS NO.1223-16-1 CAS NO.1223-16-1

    Cas No: 1223-16-1

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1223-16-1 Usage

Chemical Properties

Amber to brown liquid

Check Digit Verification of cas no

The CAS Registry Mumber 1223-16-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,2 and 3 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1223-16:
(6*1)+(5*2)+(4*2)+(3*3)+(2*1)+(1*6)=41
41 % 10 = 1
So 1223-16-1 is a valid CAS Registry Number.
InChI:InChI=1/C14H18N2O2Si/c1-19(2,17-13-7-3-11(15)4-8-13)18-14-9-5-12(16)6-10-14/h3-10H,15-16H2,1-2H3

1223-16-1SDS

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 4-[(4-aminophenoxy)-dimethylsilyl]oxyaniline

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:1223-16-1 SDS

1223-16-1Downstream Products

1223-16-1Relevant articles and documents

Curing kinetics and thermal stability of novel siloxane-containing benzoxazines

Xu, Jilei,Li, Hui,Zeng, Kai,Li, Gaoxu,Zhao, Xuhong,Zhao, Chunxia

, p. 119 - 126 (2018/11/30)

Novel siloxane-containing benzoxazines were prepared from phenol, paraformaldehyde, and bis(p-aminophenoxy)siloxane. The curing reaction of obtained benzoxazines was studied by in-situ Fourier Transform infrared spectroscopy. The curing kinetics and kinetic model were investigated by nonisothermal Differential Scanning Calorimeter. The kinetic data indicated that the activation energy shifted to a higher value with the increase in benzene ring content in benzoxazines, and the siloxane-containing benzoxazines followed an autocatalytic curing model based on Friedman method. Because of the introduction of aminophenoxysiloxane instead of aminopropylsiloxane, the siloxane-containing polybenzoxazines have a higher thermal stability as confirmed by thermogravimetric and pyrolysis analyses, especially for the bis(p-aminophenoxy)diphenylsiloxane-based polybenzoxazine with an initial decomposition temperature of 420 °C and a char yield of 74%.

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