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9H-Fluorene, 9,9-bis[4-(4-nitrophenoxy)phenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

139265-69-3

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139265-69-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 139265-69-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,2,6 and 5 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 139265-69:
(8*1)+(7*3)+(6*9)+(5*2)+(4*6)+(3*5)+(2*6)+(1*9)=153
153 % 10 = 3
So 139265-69-3 is a valid CAS Registry Number.

139265-69-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 9,9-bis[4-(4-nitrophenoxy)phenyl]fluorene

1.2 Other means of identification

Product number -
Other names 9,9-Bis[4-(4-nitrophenoxy)phenyl]-9H-fluorene

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:139265-69-3 SDS

139265-69-3Downstream Products

139265-69-3Relevant academic research and scientific papers

Symmetric and asymmetric spiro-type colorless poly(ester imide)s with low coefficients of thermal expansion, high glass transition temperatures, and excellent solution-processability

Hasegawa, Masatoshi,Takahashi, Shinya,Tsukuda, Soichi,Hirai, Tomoki,Ishii, Junichi,Yamashina, Yukari,Kawamura, Yoshinori

, p. 167 - 184 (2019)

In this work, we present several new poly(ester imide)s (PEsIs) with low coefficients of thermal expansion (CTE), excellent optical transparency, very high heat resistance (Tg), film ductility, and solution-processability. Symmetric and asymmet

Investigation of synthesis, thermal properties and curing kinetics of fluorene diamine-based benzoxazine by using two curing kinetic methods

He, Xuan-Yu,Wang, Jun,Ramdani, Noureddine,Liu, Wen-Bin,Liu, Li-Jia,Yang, Lei

, p. 51 - 58 (2013)

A novel diamine-based benzoxazine monomer containing aryl ether and bulky fluorene groups (BEF-p) was prepared from the reaction of 9,9-bis-[4-(p- aminophenoxy)-phenyl]fluorene with paraformaldehyde and phenol. The chemical structure of monomer was confirmed by Fourier-transform infrared (FTIR) and 1H and 13C nuclear magnetic resonance spectroscopy ( 1H and 13C NMR). The polymerization behavior of monomer was analyzed by differential scanning calorimetry (DSC) and FTIR. The curing kinetics was studied by non-isothermal DSC, and the kinetic parameters were determined. The autocatalytic model based on two kinetic methods (Starink-LSR method and direct LSR method) showed good agreement with experimental results. The thermal and mechanical properties of poly(BEF-p) were evaluated with DSC, dynamic mechanical thermal analysis (DMTA), and thermogravimetric analysis (TGA). The results showed that the cured polymer exhibited higher glass transition temperature (Tg) and better thermal stability compared with diaminodiphenylmethane-based benzoxazine(P-ddm), and was slightly lower than those of fluorene diamine-phenol-based polybenzoxazine (poly(BF-p)). Copyright

Bis(azobenzene) diamines and photomechanical polymers made therefrom

-

Page/Page column 21, (2017/05/31)

Bis(azo-benzene) diamine monomers and a method of synthesizing the monomers are provided. The bis(azo-benzene) diamine monomers, in combination with amine reactive monomers, form polymers, such as polyimides and copolyimides, having photomechanical and thermomechanical properties.

AROMATIC DIAMINE AND PROCESS FOR PRODUCING THE SAME

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Page/Page column 8-10, (2008/06/13)

An aromatic diamine represented by the following formula (I): (wherein R1 to R6 each independently represent hydrogen, an alkyl group or an aryl group and may be the same or different). The aromatic diamine is useful as a curing agent for a monomer such as a polyimide, polyamide or a polyamideimide, a polyurethane, an epoxy resin or the like.

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