Welcome to LookChem.com Sign In|Join Free

CAS

  • or

863027-98-9

Post Buying Request

863027-98-9 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

863027-98-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 863027-98-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,3,0,2 and 7 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 863027-98:
(8*8)+(7*6)+(6*3)+(5*0)+(4*2)+(3*7)+(2*9)+(1*8)=179
179 % 10 = 9
So 863027-98-9 is a valid CAS Registry Number.

863027-98-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-ethylhexyl)-3,6-dibromophthalimide

1.2 Other means of identification

Product number -
Other names 4,7-DibroMo-2-(2-ethylhexyl)isoindoline-1,3-dione

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:863027-98-9 SDS

863027-98-9Downstream Products

863027-98-9Relevant articles and documents

Conjugated polymers based on benzodithiophene and arylene imides: Extended absorptions and tunable electrochemical properties

Chen, Jian,Shi, Min-Min,Hu, Xiao-Lian,Wang, Mang,Chen, Hong-Zheng

experimental part, p. 2897 - 2902 (2011/11/06)

Three novel conjugated polymers have been designed and synthesized via the alternative copolymerization of the electron-donating monomer benzodithiophene (BDT) and three different electron-accepting monomers: perylene diimide (PDI), naphthalene diimide (NDI), and phthalimide (PhI). All obtained copolymers show good solubility in common organic solvents as well as broader absorptions in visible region and narrower optical band gaps compared to homopolymers from BDT units. It is found that the absorptions of the copolymers are red-shifted with increasing the electron-withdrawing ability of the co-monomer. In particular, the absorption edge of P(BDT-NDI) film extends to 760. nm, whereas that of P(BDT-PhI) film is only at 577. nm. Cyclic voltammograms of the three polymers disclose that P(BDT-PDI) and P(BDT-NDI) are typical n-type materials because PDI and NDI are strong electron-accepting groups, while P(BDT-PhI) is a stable p-type material where the weak electron-withdrawing monomer (PhI) is introduced. The results suggest that the absorption range and the electrochemical properties of the conjugated polymers can be tuned by appropriate molecule-tailoring, which will help exploring ideal conducting polymers for potential applications in polymer optoelectronics, especially in polymer solar cells.

Phthalimide-based polymers for high performance organic thin-film transistors

Guo, Xugang,Kim, Felix Sunjoo,Jenekhe, Samson A.,Watson, Mark D.

supporting information; experimental part, p. 7206 - 7207 (2009/10/16)

-

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 863027-98-9