4789-44-0

Basic information

• Product Name: 1H-Pyrrole-2-carboxylicacid, 5-(bromomethyl)-4-ethyl-3-methyl-, ethyl ester
• Synonyms: Pyrrole-2-carboxylicacid, 5-(bromomethyl)-4-ethyl-3-methyl-, ethyl ester (6CI,7CI,8CI)
• CAS NO: 4789-44-0
• Molecular Formula: C11H16 Br N O2
• Molecular Weight: 274.158
• Mol File: 4789-44-0.mol
• Article Data: 0

Chemical Properties

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Density: 1.66g/cm³
• CAS DataBase Reference: 1H-Pyrrole-2-carboxylicacid, 5-(bromomethyl)-4-ethyl-3-methyl-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Pyrrole-2-carboxylicacid, 5-(bromomethyl)-4-ethyl-3-methyl-, ethyl ester(4789-44-0)
• EPA Substance Registry System: 1H-Pyrrole-2-carboxylicacid, 5-(bromomethyl)-4-ethyl-3-methyl-, ethyl ester(4789-44-0)

Safety Data

• Hazardous Substances Data: 4789-44-0(Hazardous Substances Data)

Usage

Molecular structure

1H-Pyrrole-2-carboxylic acid, 5-(bromomethyl)-4-ethyl-3-methyl-, ethyl ester is a heterocyclic compound with a five-membered ring consisting of four carbon atoms and one nitrogen atom. The ethyl ester group is attached to the carboxylic acid, and the bromomethyl and methyl groups are attached to the 5th and 3rd carbon atoms respectively, while the 4th carbon has an ethyl group.

Functional groups

The compound contains several functional groups, including a pyrrole ring, a carboxylic acid group, an ethyl ester group, a bromomethyl group, and an ethyl group.

Physical state

The compound is likely a solid at room temperature, as most organic compounds with similar structures are.

Polarity

The presence of polar functional groups such as the carboxylic acid and ester groups make the compound polar.

Reactivity

The compound is likely to undergo various chemical reactions due to the presence of reactive functional groups such as the carboxylic acid and bromomethyl groups. It can participate in reactions such as esterification, bromination, and substitution reactions.

Synthesis

The compound is commonly used in organic synthesis and pharmaceutical research, and may be used as a building block in the synthesis of various organic molecules.

Potential applications

The compound may have potential applications in the development of new drugs or materials due to its unique structure and reactivity.

Solubility

The compound may be soluble in common organic solvents such as ethanol, methanol, or dichloromethane, but its exact solubility will depend on its physical state and the solvent's properties.

Downstream Products

• 109451-58-3 (5-ethoxycarbonyl-3-ethyl-4-methyl-pyrrol-2-ylmethyl)-pyridinium; bromide 
• 15769-97-8 5-Ethoxycarbonyl-3,4'-diethyl-3',4,5'-trimethyl-2,2'-dipyrrylmethan 
• 124422-22-6 4,4'-diethyl-3,3'-dimethyl-5,5'-(4-ethyl-5-bromo-3,5-dimethyl-1,5-dihydro-pyrrole-2,2-diyldimethyl)-bis-pyrrole-2-carboxylic acid ethyl ester-benzyl ester 
• 102319-89-1 4-ethyl-5-(4-dimethylamino-benzyl)-3-methyl-pyrrole-2-carboxylic acid ethyl ester 
• 101737-85-3 4-ethyl-3-methyl-5-[(N-methyl-anilino)-methyl]-pyrrole-2-carboxylic acid ethyl ester 
• 102443-44-7 4-ethyl-5-(4-diethylamino-benzyl)-3-methyl-pyrrole-2-carboxylic acid ethyl ester 
• 6305-93-7 [5,5'-bis(ethoxycarbonyl)-3,3'-diethyl-4,4'-dimethyl-2,2'-dipyrrolyl]methane 
• 4391-87-1 ethyl 4-ethyl-5-formyl-3-methylpyrrole-2-carboxylate 
• 448-71-5 ethioporphyrin I 
• 101782-28-9 4-ethyl-5-benzyloximethyl-3-methyl-pyrrole-2-carboxylic acid ethyl ester