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Pyrrolo[3,4-c]pyrrole-1,4-dione, 2,5-dihydro-3,6-bis[4-(trifluoromethyl)phenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88949-31-9

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88949-31-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88949-31-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,9,4 and 9 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 88949-31:
(7*8)+(6*8)+(5*9)+(4*4)+(3*9)+(2*3)+(1*1)=199
199 % 10 = 9
So 88949-31-9 is a valid CAS Registry Number.

88949-31-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,6-bis[4-(trifluoromethyl)phenyl]-2,5-dihydropyrrolo[3,4-c]-pyrrole-1,4-dione

1.2 Other means of identification

Product number -
Other names 2,5-dihydro-3,6-bis(4-trifluoromethylphenyl)pyrrolo[3,4-c]pyrrole-1,4-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:88949-31-9 SDS

88949-31-9Relevant academic research and scientific papers

Effects of Fluorine Substitution on the Intermolecular Interactions, Energetics, and Packing Behavior of N-Benzyl Substituted Diketopyrrolopyrroles

Calvo-Castro, Jesus,Morris, Graeme,Kennedy, Alan R.,McHugh, Callum J.

, p. 2371 - 2384 (2016)

Rationalizing the effects of molecular substitution in π-conjugated organic materials arising from well-defined intermolecular interactions, which can influence the formation of predefined packing motifs and control the emergence of π-π stacking represent

Beauty in chemistry: A self-organized and dual-phase emissive diketopyrrolopyrrole derivative as high-yield fluorescent material

Han, Jianwei,Sun, Xinyu,Wang, Limin,Yang, Qingying

, (2021/08/03)

In the long-span human history, “beauty” has always been the ultimate pursuit of mankind's civilization. In this work, we report the synthesis of a beautiful fluorescent material based on an old-brand pigment named diketopyrrolopyrrole (DPP) with a high y

Diketopyrrolopyrrole-based cyclic compound with solid-liquid bifluorescence, preparation method of cyclic compound and application of cyclic compound

-

Paragraph 0051-0053, (2019/07/01)

The invention discloses a diketopyrrolopyrrole-based cyclic compound with solid-liquid bifluorescence. The structure of the cyclic compound is as shown in the specification, R is H, CN, nitro, halogen, alkyl, substituted alkyl, alkoxy and substituted alko

Fluorine-bearing diketopyrrolopyrrole quaternary ammonium salt compound and preparation method and application thereof

-

Paragraph 0107; 0109-0111, (2019/07/01)

The invention discloses a fluorine-bearing diketopyrrolopyrrole quaternary ammonium salt compound, having a structure shown as the formula (I) which is shown in the description, wherein R1 is one of F, CH2F, CHF2, CF3, OCH2F, OCHF2, OCF3, SCH2F, SCHF2, SC

Rational synthesis and comparative investigation on a series of fluorinated aryl substituted diketopyrrolopyrrole

Xu, Jie,Zhang, Shaoze,Wu, Shengying,Bi, Shiming,Li, Xinjin,Lu, Yunxiang,Wang, Limin

, p. 494 - 499 (2017/01/14)

We novelly designed and synthesized a set of fluorinated diphenyl-diketopyrrolopyrrole (DPP) compounds by varying the position and amount of fluorine atom, and to the best of our knowledge, it is the first time a difluoromethyl group and perfluoroalkyl ch

Synthesis and n-type field-effect transistor characteristics of dioxopyrrolopyrrole derivatives

Suna, Yuki,Nishida, Jun-Ichi,Fujisaki, Yoshihide,Yamashita, Yoshiro

supporting information; experimental part, p. 822 - 824 (2011/09/14)

Dioxopyrrolopyrrole derivatives with electron-withdrawing groups have been synthesized and applied to organic field-effect transistors as n-channel semiconductors. A derivative with an intermolecular hydrogen-bonding network showed a good electron mobility up to 2.9 1012 cm2V 11 s11.

SOLVENT-FREE PROCESS FOR THE PREPARATION OF DIKETOPYRROLOPYRROLE DERIVATIVES

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Page 17, (2010/02/08)

The present application relates to compounds of formula A(D)X(E)y, (I), compounds of formula (III), compounds of formula (X), as well as processes for the preparation thereof, processes where the compounds (I) are converted to pigments of formula (II) and the use of the compounds (I).

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