1378389-49-1

Basic information

• Product Name: (2S,4S)-tert-butyl 2-(5-bromo-1H-imidazol-2-yl)-4-(methoxymethyl)pyrrolidine-1-carboxylate
• CAS NO: 1378389-49-1
• Molecular Weight: 360.251
• Mol File: 1378389-49-1.mol
• Article Data: 0

Chemical Properties

• CAS DataBase Reference: (2S,4S)-tert-butyl 2-(5-bromo-1H-imidazol-2-yl)-4-(methoxymethyl)pyrrolidine-1-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,4S)-tert-butyl 2-(5-bromo-1H-imidazol-2-yl)-4-(methoxymethyl)pyrrolidine-1-carboxylate(1378389-49-1)
• EPA Substance Registry System: (2S,4S)-tert-butyl 2-(5-bromo-1H-imidazol-2-yl)-4-(methoxymethyl)pyrrolidine-1-carboxylate(1378389-49-1)

Safety Data

• Hazardous Substances Data: 1378389-49-1(Hazardous Substances Data)

Usage

Description

(2S,4S)-tert-butyl 2-(5-bromo-1H-imidazol-2-yl)-4-(methoxymethyl)pyrrolidine-1-carboxylate is a complex organic chemical compound characterized by a pyrrolidine ring fused with an imidazole ring. This derivative of pyrrolidine-1-carboxylic acid features a tert-butyl group attached to the nitrogen atom of the pyrrolidine ring, enhancing its steric hindrance and potentially affecting its reactivity and stability. The presence of a 5-bromo-1H-imidazol-2-yl group and a methoxymethyl group on different carbon atoms of the pyrrolidine ring introduces additional functional groups and structural diversity, which may endow the compound with unique chemical and biological properties. These attributes render it a candidate of interest for pharmaceutical development and scientific research.

Uses

Used in Pharmaceutical Development:
(2S,4S)-tert-butyl 2-(5-bromo-1H-imidazol-2-yl)-4-(methoxymethyl)pyrrolidine-1-carboxylate is utilized as a lead compound in drug discovery for its potential pharmacological activity. (2S,4S)-tert-butyl 2-(5-bromo-1H-imidazol-2-yl)-4-(methoxymethyl)pyrrolidine-1-carboxylate's unique structure, including the bromo and methoxymethyl substituents, may confer specific binding affinities and selectivity towards biological targets, such as enzymes or receptors, relevant to various therapeutic areas.
Used in Scientific Research:
In the field of organic chemistry and medicinal chemistry, (2S,4S)-tert-butyl 2-(5-bromo-1H-imidazol-2-yl)-4-(methoxymethyl)pyrrolidine-1-carboxylate serves as a valuable research tool. It can be employed to study the effects of structural modifications on the compound's reactivity, stability, and biological activity. Furthermore, it may be used to investigate novel synthetic routes and methodologies for the preparation of related pyrrolidine and imidazole derivatives with potential applications in various industries.
Used in Chemical Synthesis:
(2S,4S)-tert-butyl 2-(5-bromo-1H-imidazol-2-yl)-4-(methoxymethyl)pyrrolidine-1-carboxylate is used as an intermediate in the synthesis of more complex organic molecules. Its unique functional groups and stereochemistry make it a versatile building block for the preparation of pharmaceuticals, agrochemicals, or other specialty chemicals that require the pyrrolidine and imidazole motifs.
Used in Material Science:
(2S,4S)-tert-butyl 2-(5-bromo-1H-imidazol-2-yl)-4-(methoxymethyl)pyrrolidine-1-carboxylate may also find applications in material science, where its structural features could be exploited to develop new materials with specific properties. For instance, its potential use in the design of polymers, coatings, or sensors could be explored, taking advantage of its chemical reactivity and the possibility of forming supramolecular assemblies.

Downstream Products

• 1377049-57-4 methyl {(1R)-2-[(2S,4S)-2-(5-{2-[(2S)-1-{(2S)-2-[(methoxycarbonyl)amino]-3-methylbutanoyl}-pyrrolidin-2-yl]-1,11-dihydroisochromeno[4′,3′:6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-4-(methoxymethyl)pyrrolidin-1-yl]-2-oxo-1-phenylethyl}carbamate