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4-BROMO-3,5-DIMETHYL-1H-PYRROLE-2-CARBALDEHYDE is a chemical compound characterized by its molecular formula C8H8BrNO. It is an aldehyde derivative of pyrrole, a five-membered aromatic heterocycle. 4-BROMO-3,5-DIMETHYL-1H-PYRROLE-2-CARBALDEHYDE is notable for its potential applications in various fields due to its unique structure and properties.

89909-51-3

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89909-51-3 Usage

Uses

Used in Organic Synthesis:
4-BROMO-3,5-DIMETHYL-1H-PYRROLE-2-CARBALDEHYDE is used as a building block in organic synthesis, particularly for the creation of pharmaceuticals and agrochemicals. Its structural features make it a valuable intermediate in the development of new compounds with specific biological activities.
Used in Polymer and Material Science:
In the field of polymer and material science, 4-BROMO-3,5-DIMETHYL-1H-PYRROLE-2-CARBALDEHYDE is utilized in the preparation of pyrrole-based polymers and materials. These polymers can exhibit a range of properties, such as conductivity or specific binding affinities, which are useful in various applications.
Used in Organic Electronics and Optoelectronics:
4-Bromo-3,5-dimethyl-1H-pyrrole-2-carbaldehyde has potential applications in the field of organic electronics and optoelectronics. Its electronic and photophysical properties make it a candidate for use in devices such as organic light-emitting diodes (OLEDs), photovoltaic cells, and other electronic components that require materials with specific electronic characteristics.

Check Digit Verification of cas no

The CAS Registry Mumber 89909-51-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,9,0 and 9 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 89909-51:
(7*8)+(6*9)+(5*9)+(4*0)+(3*9)+(2*5)+(1*1)=193
193 % 10 = 3
So 89909-51-3 is a valid CAS Registry Number.

89909-51-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-BROMO-3,5-DIMETHYL-1H-PYRROLE-2-CARBALDEHYDE

1.2 Other means of identification

Product number -
Other names 1H-Pyrrole-2-carboxaldehyde,4-bromo-3,5-dimethyl

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:89909-51-3 SDS

89909-51-3Downstream Products

89909-51-3Relevant academic research and scientific papers

Indolin-2-ones with high in vivo efficacy in a model for multiple sclerosis

Bouérat, La?titia,Fensholdt, Jef,Liang, Xifu,Havez, Sophie,Nielsen, Simon F.,Hansen, Jens R.,Bolvig, Simon,Andersson, Christina

, p. 5412 - 5414 (2005)

The known KDR inhibitor SU5416 and several analogues of the indolin-2-one family were surprisingly found to be highly efficacious in the EAE model, an established model for multiple sclerosis. The high in vivo effect could be correlated to in vitro inhibi

TAMBJAMINES AND B-RING FUNCTIONALIZED PRODIGININES

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Page/Page column 19; 20; 30; 31, (2016/11/17)

Embodiments of tambjamines and B-ring functionalized prodiginines are disclosed. Methods of synthesizing and using the disclosed compounds are also disclosed. Some embodiments of the disclosed compounds have antimalarial activity. Certain embodiments of t

Synthesis and Structure-Activity Relationships of Tambjamines and B-Ring Functionalized Prodiginines as Potent Antimalarials

Kancharla, Papireddy,Kelly, Jane Xu,Reynolds, Kevin A.

, p. 7286 - 7309 (2015/10/05)

Synthesis and antimalarial activity of 94 novel bipyrrole tambjamines (TAs) and a library of B-ring functionalized tripyrrole prodiginines (PGs) against a panel of Plasmodium falciparum strains are described. The activity and structure-activity relationsh

NOVEL THERAPEUTIC USE OF INDOLINONE DERIVATIVES

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Page/Page column 62, (2010/02/12)

Certain oxindole compounds have been found to be effective in experimentally induced autoimmune encephalitis and are therefore suggested for the preparation of a medicament for the prevention, treatment or amelioration of multiple sclerosis, or to delay the onset of or reduce the relapse rate in multiple sclerosis.

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