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BIS(4-MALEIMIDOPHENYL)SULFONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13102-25-5

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13102-25-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13102-25-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,0 and 2 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 13102-25:
(7*1)+(6*3)+(5*1)+(4*0)+(3*2)+(2*2)+(1*5)=45
45 % 10 = 5
So 13102-25-5 is a valid CAS Registry Number.

13102-25-5SDS

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 1-[4-[4-(2,5-dioxopyrrol-1-yl)phenyl]sulfonylphenyl]pyrrole-2,5-dione

1.2 Other means of identification

Product number -
Other names N,N'-4,4'-Diphenylsulfon-bis-maleimid

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:13102-25-5 SDS

13102-25-5Relevant academic research and scientific papers

Thermally amendable tailor-made functional polymer by RAFT polymerization and "click reaction"

Pramanik, Nabendu B.,Bag, Dibyendu S.,Alam, Sarfaraz,Nando, Golok B.,Singha, Nikhil K.

, p. 3365 - 3374 (2013)

This investigation reports the preparation and characterization of thermally amendable functional polymer bearing furfuryl functionality via reversible-addition fragmentation and chain transfer (RAFT) polymerization and Diels-Alder (DA) reaction. In this

Cardanol based benzoxazine blends and bio-silica reinforced composites: Thermal and dielectric properties

Arumugam,Krishnan,Chavali,Muthukaruppan

, p. 4067 - 4080 (2018/03/21)

In the present work, a novel cardanol based benzoxazine was synthesised by reacting three different amines (aniline (CrAb), N,N-dimethylaminopropylamine (CrDb) and caprolactam modified N,N-dimethylaminopropylamine (CrCb)) with cardanol in the presence of formaldehyde under appropriate experimental conditions. The resulting benzoxazines were characterised for their molecular structure and thermal behaviour using different analytical methods. Among the different systems studied, the tertiary amine derivatives were found to reduce the curing temperature efficiently (CrAb-275 °C > CrDb-265 °C > CrCb-251 °C) and were confirmed by DSC analysis. These cardanol based CrAb benzoxazines were blended with conventional benzoxazines (Bzs) and bismaleimides (BMIs) as binary and ternary systems and their thermal properties were studied. Three different catalysts (4-hydroxy acetophenone, 4-aminophenol, and 4-hydroxyphenyl maleimide) were used to study the effect of lowering the curing temperature. Further, the prepared benzoxazines were reinforced with varying weight percentages (1, 3, 5 and 10 wt%) of bio-silica derived from rice husk to obtain hybrid composites. The dielectric studies of bio-silica reinforced cardanol benzoxazines infer that the values of dielectric constant decreased with increasing wt% of bio-silica. It was further observed that 10 wt% bio-silica reinforced cardanol benzoxazines show the lowest value of dielectric constant of 1.9 at 1 MHz. From the data obtained from the different studies, it is concluded that the blends of cardanol based benzoxazines can be used in the form of sealants, encapsulants, adhesives and matrices in the fields of microelectronics and automobile applications for better performance.

Synthesis, cure and thermal properties of bismaleimide resin and allylnadic-imide

Singh,Sharma, Hariom

, p. 1389 - 1397 (2013/02/25)

Synthesis of Bismaleimide i.e. bis (4-maleimidophenyl) Sulphone (B) and Michael adduct of B with 4,42 - Di amino Diphenyl methane and blended with allylnadicimides i.e. bis (4-allylnadicimidophenyl) methane (S),1,6- allylnadicimidohexane(V), and N-allylna

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