174575-06-5

Usage

Core structure

Imidazolidinecarboxylic acid
A five-membered ring containing two nitrogen atoms and one carbon atom, with a carboxyl group (-COOH) attached to it.

Bromine substitution

3-Bromo-5-[(diethoxyphosphinyl)methyl]phenyl
A bromine atom (Br) is attached to a phenyl ring (a six-membered carbon ring with alternating single and double bonds), which is connected to a diethoxyphosphinyl methyl group.

Diethoxyphosphinyl methyl linkage

A phosphorus atom bonded to two ethoxy groups (-OCH3) and a methyl group (-CH3) that connects the phenyl ring to the imidazolidinecarboxylic acid core.

Acylation

1,1-Dimethylethyl ester
A 1,1-dimethylethyl group (two methyl groups attached to a single carbon atom) is esterified to the carboxyl group of the imidazolidinecarboxylic acid, forming an ester bond (-COO-).

Stereochemistry

(2S-trans)
The compound exists in a specific three-dimensional arrangement, with the S (s) configuration at the second carbon atom and the trans (E) configuration, indicating that the bromine-substituted phenyl group and the 1,1-dimethylethyl ester group are on opposite sides of the imidazolidine ring.

Potential applications

The compound may have applications in various fields, including pharmaceuticals, agrochemicals, and materials science. However, further research and experimentation are needed to determine its exact uses and properties.

Upstream product

• 51760-22-6 5-bromo-1,3-dihydroxymethylbenzene 
• 51760-23-7 1-bromo-3,5-bis(bromomethyl)benzene 
• 119838-38-9 (2S)-1-(tert-butyloxycarbonyl)-2-tert-butyl-3-methylimidazolidin-4-one 
• 174575-03-2 diethyl <<3-bromo-5-(bromomethyl)phenyl>methyl>phosphonate 

Downstream Products

• 174575-22-5 (2S,5S)-2-tert-Butyl-5-[2',4'-dichloro-5-(diethoxy-phosphorylmethyl)-biphenyl-3-ylmethyl]-3-methyl-4-oxo-imidazolidine-1-carboxylic acid tert-butyl ester 
• 142184-04-1 1,1-dimethylethyl (2S,5S)-5-<<5-<(diethoxyphosphoryl)methyl><1,1'-biphenyl>-3-yl>methyl>-2-(1,1-dimethylethyl)-3-methyl-4-oxoimidazolidine-1-carboxylate 
• 174575-09-8 1,1-dimethylethyl (2S,5S)-5-<<5-<(diethoxyphopsphoryl)methyl>-4'-hydroxy(1,1'-biphenyl)-3-yl>methyl>-2-(1,1-dimethylethyl)-3-methyl-4-oxoimidazolidine-1-carboxylate 
• 174575-17-8 SDZ 220-581 
• 118077-09-1 (S)-α-amino-5-(phosphonomethyl)<1,1'-biphenyl>-3-propanoic acid 
• 174575-10-1 (2S,5S)-5-[4'-Benzyloxy-5-(diethoxy-phosphorylmethyl)-biphenyl-3-ylmethyl]-2-tert-butyl-3-methyl-4-oxo-imidazolidine-1-carboxylic acid tert-butyl ester 
• 174575-08-7 1,1-dimethylethyl (2S,5S)-5-<<2'-chloro-5-<(diethoxyphopsphoryl)methyl>(1,1'-biphenyl)-3-yl>methyl>-2-(1,1-dimethylethyl)-3-methyl-4-oxoimidazolidine-1-carboxylate 
• 174575-21-4 (2S,5S)-2-tert-Butyl-5-[5-(diethoxy-phosphorylmethyl)-2'-fluoro-biphenyl-3-ylmethyl]-3-methyl-4-oxo-imidazolidine-1-carboxylic acid tert-butyl ester 
• 174575-16-7 (2S,5S)-2-tert-Butyl-5-[5-(diethoxy-phosphorylmethyl)-2'-methyl-biphenyl-3-ylmethyl]-3-methyl-4-oxo-imidazolidine-1-carboxylic acid tert-butyl ester 

Relevant academic research and scientific papers

Syntheses of biphenyl analogues of AP7, a new class of competitive N-methyl-D-aspartate (NMDA) receptor antagonists

Affinities for the NMDA receptor were measured ([3H]CGP-39653 binding assay) and competitive NMDA antagonistic potencies determined in a functional test (rat neocortical slice preparation). Structure-activity relationships show that attachment