Welcome to LookChem.com Sign In|Join Free

CAS

  • or
2H-Indol-2-one, 6-bromo-3-[6-bromo-1,2-dihydro-1-(2-octyldodecyl)-2-oxo-3H-indol-3-ylidene]-1,3-dihydro-1-(2-octyldodecyl)is a complex organic compound characterized by its indolone rings and bromine substitutions. This molecule features two indolone rings, one of which is substituted with a bromine atom, and a long 2-octyldodecyl alkyl chain. The presence of bromine atoms endows the compound with enhanced reactivity, making it a candidate for various chemical reactions. Its unique structure also suggests potential applications in organic synthesis and as a component in the construction of more intricate molecular architectures.

1263379-85-6

Post Buying Request

1263379-85-6 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 2H-indol-2-one, 6-bromo-3-[6-bromo-1,2-dihydro-1-(2-octyldodecyl)-2-oxo-3h-indol-3-ylidene]-1,3-dihydro-1-(2-octyldodecyl)-;1263379-85-6

    Cas No: 1263379-85-6

  • No Data

  • 10 Metric Ton

  • Metric Ton/Day

  • Amadis Chemical Co., Ltd.
  • Contact Supplier
  • 2H-Indol-2-one, 6-bromo-3-[6-bromo-1,2-dihydro-1-(2-octyldodecyl)-2-oxo-3H-indol-3-ylidene]-1,3-dihydro-1-(2-octyldodecyl)-

    Cas No: 1263379-85-6

  • USD $ 1.9-2.9 / Gram

  • 100 Gram

  • 1000 Metric Ton/Month

  • Chemlyte Solutions
  • Contact Supplier

1263379-85-6 Usage

Uses

Used in Organic Synthesis:
2H-Indol-2-one, 6-bromo-3-[6-bromo-1,2-dihydro-1-(2-octyldodecyl)-2-oxo-3H-indol-3-ylidene]-1,3-dihydro-1-(2-octyldodecyl)is utilized as a building block in organic synthesis for the creation of more complex molecules. Its bromine atoms facilitate various chemical reactions, such as cross-coupling and substitution, enabling the synthesis of novel compounds with diverse properties and applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2H-Indol-2-one, 6-bromo-3-[6-bromo-1,2-dihydro-1-(2-octyldodecyl)-2-oxo-3H-indol-3-ylidene]-1,3-dihydro-1-(2-octyldodecyl)is employed as a precursor for the development of new drugs. Its unique structure and reactivity allow for the design of molecules with potential therapeutic effects, targeting various diseases and medical conditions.
Used in Chemical Research:
2H-Indol-2-one, 6-bromo-3-[6-bromo-1,2-dihydro-1-(2-octyldodecyl)-2-oxo-3H-indol-3-ylidene]-1,3-dihydro-1-(2-octyldodecyl)serves as a valuable compound in chemical research, particularly in the study of indolone chemistry and the exploration of novel reaction mechanisms. Its structure provides insights into the properties and behavior of similar compounds, contributing to the advancement of chemical knowledge and the discovery of new synthetic routes.

Check Digit Verification of cas no

The CAS Registry Mumber 1263379-85-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,3,3,7 and 9 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1263379-85:
(9*1)+(8*2)+(7*6)+(6*3)+(5*3)+(4*7)+(3*9)+(2*8)+(1*5)=176
176 % 10 = 6
So 1263379-85-6 is a valid CAS Registry Number.

1263379-85-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2H-Indol-2-one, 6-bromo-3-[6-bromo-1,2-dihydro-1-(2-octyldodecyl)-2-oxo-3H-indol-3-ylidene]-1,3-dihydro-1-(2-octyldodecyl)-

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:1263379-85-6 SDS

1263379-85-6Relevant articles and documents

Acceptor-acceptor type isoindigo-based copolymers for high-performance n-channel field-effect transistors

Kim, Gyoungsik,Han, A-Reum,Lee, Hae Rang,Lee, Junghoon,Oh, Joon Hak,Yang, Changduk

, p. 2180 - 2183 (2014/02/14)

Two acceptor-acceptor (A-A) type copolymers (PIIG-BT and PIIG-TPD) with backbones composed exclusively of electron-deficient units are designed and synthesized. Both copolymers show unipolar n-type operations. In particular, PIIG-BT shows electron mobility of up to 0.22 cm2 V-1 s-1. This is a record value for n-type copolymers based on lactam cores. The Royal Society of Chemistry.

A thienoisoindigo-naphthalene polymer with ultrahigh mobility of 14.4 cm2/V·s that substantially exceeds benchmark values for amorphous silicon semiconductors

Kim, Gyoungsik,Kang, Seok-Ju,Dutta, Gitish K.,Han, Young-Kyu,Shin, Tae Joo,Noh, Yong-Young,Yang, Changduk

supporting information, p. 9477 - 9483 (2014/07/21)

By considering the qualitative benefits associated with solution rheology and mechanical properties of polymer semiconductors, it is expected that polymer-based electronic devices will soon enter our daily lives as indispensable elements in a myriad of flexible and ultra low-cost flat panel displays. Despite more than a decade of research focused on designing and synthesizing state-of-the-art polymer semiconductors for improving charge transport characteristics, the current mobility values are still not sufficient for many practical applications. The confident mobility in excess of ~10 cm2/V·s is the most important requirement for enabling the realization of the aforementioned near-future products. We report on an easily attainable donor-acceptor (D-A) polymer semiconductor: poly(thienoisoindigo-alt- naphthalene) (PTIIG-Np). An unprecedented mobility of 14.4 cm 2/V·s, by using PTIIG-Np with a high-k gate dielectric poly(vinylidenefluoride-trifluoroethylene) (P(VDF-TrFE)), is achieved from a simple coating processing, which is of a magnitude that is very difficult to obtain with conventional TFTs by means of molecular engineering. This work, therefore, represents a major step toward truly viable plastic electronics.

Systematic investigation of isoindigo-based polymeric field-effect transistors: Design strategy and impact of polymer symmetry and backbone curvature

Lei, Ting,Cao, Yue,Zhou, Xu,Peng, Yang,Bian, Jiang,Pei, Jian

scheme or table, p. 1762 - 1770 (2012/08/07)

Ten isoindigo-based polymers were synthesized, and their photophysical and electrochemical properties and device performances were systematically investigated. The HOMO levels of the polymers were tuned by introducing different donor units, yet all polymers exhibited p-type semiconducting properties. The hole mobilities of these polymers with centrosymmetric donor units exceeded 0.3 cm2 V-1 s-1, and the maximum reached 1.06 cm2 V-1 s-1. Because of their low-lying HOMO levels, these copolymers also showed good stability upon moisture. AFM and GIXD analyses revealed that polymers with different symmetry and backbone curvature were distinct in lamellar packing and crystallinity. DFT calculations were employed to help us propose the possible packing model. Based on these results, we propose a design strategy, called molecular docking , to understand the interpolymer π-π stacking. We also found that polymer symmetry and backbone curvature affect interchain molecular docking of isoindigo-based polymers in film, ultimately leading to different device performance. Finally, our design strategy maybe applicable to other reported systems, thus representing a new concept to design conjugated polymers for field-effect transistors.

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 1263379-85-6