94781-48-3

Basic information

• Product Name: 1H-Pyrrole-2-carboxaldehyde, 4-bromo-3-methyl-
• Synonyms: 4-Bromo-3-methyl-1H-pyrrole-2-carbaldehyde;4-bromo-2-formyl-3-methylpyrrole;4-bromo-3-methyl-1H-Pyrrole-2-carboxaldehyde
• CAS NO: 94781-48-3
• Molecular Formula: C6H6BrNO
• Molecular Weight: 188.024
• Mol File: 94781-48-3.mol

Chemical Properties

• CAS DataBase Reference: 1H-Pyrrole-2-carboxaldehyde, 4-bromo-3-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Pyrrole-2-carboxaldehyde, 4-bromo-3-methyl-(94781-48-3)
• EPA Substance Registry System: 1H-Pyrrole-2-carboxaldehyde, 4-bromo-3-methyl-(94781-48-3)

Safety Data

• Hazardous Substances Data: 94781-48-3(Hazardous Substances Data)

Usage

Structure

A five-membered heterocyclic ring containing nitrogen, with a carboxaldehyde group at position 2, a bromine atom at position 4, and a methyl group at position 3.

Type

A derivative of pyrrole.

Usage

Used in organic synthesis and pharmaceutical applications, commonly as an intermediate in the synthesis of various biologically active compounds and pharmaceutical drugs.

Potential

Studied for its potential use in the development of new materials and chemical processes.

Upstream product

• 89909-42-2 4-bromo-3-methyl-1H-pyrrole-2-carboxylic acid ethyl ester 
• 24014-18-4 3-methyl-pyrrole-2-carboxaldehyde 

Downstream Products

• 1284257-65-3 4-bromo-3-methyl-2-(2-nitroethyl)-N-tosylpyrrole 
• 1284257-67-5 6-(4-bromo-3-methyl-N-tosylpyrrol-2-yl)-1,1-dimethoxy-4,4-dimethyl-5-nitrohexan-2-one 
• 1284257-69-7 4-bromo-3-methyl-2-formyl-N-tosylpyrrole 

Relevant articles and documents

TAMBJAMINES AND B-RING FUNCTIONALIZED PRODIGININES

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

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

BACTERIOCHLORIN IMIDES

Compound of Formula I: are described, along with compositions containing the same and methods of use thereof.

De novo synthesis and photophysical characterization of annulated bacteriochlorins. Mimicking and extending the properties of bacteriochlorophylls

Bacteriochlorophylls contain the bacteriochlorin chromophore and a fifth, five-membered oxopentano ring that encompasses positions 13-15 known as the "isocyclic" ring E. Such bacterio-131-oxophorbines have heretofore only been available in the

Novel Substituent Orientation in Reimer-Tiemann Reactions of Pyrrole-2-carboxylates

Reimer-Tiemann formylation reactions (base/CHCl3) on 5-substituted pyrrole-2-carboxylates (1, 6, 8, 9, 11, and 13) afford 2-formylpyrroles (5, 7, 10, 12, and 14) in which the formyl group is situated in the position originally occupied by the carboxylate