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13080-88-1

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13080-88-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13080-88-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,8 and 0 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 13080-88:
(7*1)+(6*3)+(5*0)+(4*8)+(3*0)+(2*8)+(1*8)=81
81 % 10 = 1
So 13080-88-1 is a valid CAS Registry Number.

13080-88-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name bis-[4-(4-amino-phenoxy)-phenyl]-ether

1.2 Other means of identification

Product number -
Other names bis[4-(4-aminophenoxy)phenyl]ether

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:13080-88-1 SDS

13080-88-1Relevant articles and documents

Thermal transition behaviors, solubility, and mechanical properties of wholly aromatic para -, meta -poly(ether-amide)s: Effect on numbers of para -aryl ether linkages

Zhang, Wen-Qiang,Wang, Xiu-Li,Liu, Gui-Cheng,Chen, Li,Wang, Yu-Zhong

, p. 84284 - 84293 (2016/10/12)

In order to make clear how the numbers of para-aryl ether linkages affect the solubility, thermal transition behavior and mechanical properties of para-(p-PEAs), meta-poly(ether-amide)s (m-PEAs), a series of para-substituted aryl ether diamine monomers with 2, 3, 4 or 5 ether linkages were synthesized, and then reacted with terephthalic acid and isophthalic acid via the Yamazaki-Higashi phosphorylation method to prepare wholly aromatic PEAs. The PEAs with intrinsic viscosity values in the range of 0.81-1.16 dL g-1 were obtained and characterized by FT-IR, NMR, and elemental analysis. Although the Tgs and Tms of PEAs decrease with the increasing numbers of aryl ether linkages, their Tgs and Tms still are above 180 °C and 320 °C, respectively. p-PEAs have a high crystallinity making it difficult to dissolve them in common organic solvents even when 5 aryl ether linkages are introduced. Conversely, except for m-PEA5 with a lower polarity, the other m-PEAs show good solubility due to their low crystallinity. Besides, the decomposition temperatures at 5% weight loss of all PEAs exceed 430 °C and their residual yields at 700 °C are above 50% in N2, illustrating that they have excellent thermal stability. It is found that by casting m-PEAs DMAc solution in a dish, the transparent films with high Young's modulus (2.6-3.5 GPa) can be successfully obtained.

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