612820-01-6

Basic information

• Product Name: (2S,4S)-1-TERT-BUTYL 2-METHYL 4-BENZYL-5-OXOPYRROLIDINE-1,2-DICARBOXYLATE
• Synonyms: (2S,4S)-1-TERT-BUTYL 2-METHYL 4-BENZYL-5-OXOPYRROLIDINE-1,2-DICARBOXYLATE;(2S,4S)-1-tert-butyl 2-Methyl 4-phenoxypyrrolidine-1,2-dicarboxylate;(2S,4R)-5-Oxo-4-(phenylmethyl)-1,2-pyrrolidinedicarboxylic acid 1-(1,1-dimethylethyl) 2-methyl ester;(2S,4R)-1-tert-butyl 2-methyl 4-phenoxypyrrolidine-1,2-dicarboxylate
• CAS NO: 612820-01-6
• Molecular Formula: C₁₈H₂₃NO₅
• Molecular Weight: 333.382
• Mol File: 612820-01-6.mol

Chemical Properties

• Melting Point: 98-99℃
• Appearance: /
• CAS DataBase Reference: (2S,4S)-1-TERT-BUTYL 2-METHYL 4-BENZYL-5-OXOPYRROLIDINE-1,2-DICARBOXYLATE(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,4S)-1-TERT-BUTYL 2-METHYL 4-BENZYL-5-OXOPYRROLIDINE-1,2-DICARBOXYLATE(612820-01-6)
• EPA Substance Registry System: (2S,4S)-1-TERT-BUTYL 2-METHYL 4-BENZYL-5-OXOPYRROLIDINE-1,2-DICARBOXYLATE(612820-01-6)

Safety Data

• Hazardous Substances Data: 612820-01-6(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
(2S,4S)-1-TERT-BUTYL 2-METHYL 4-BENZYL-5-OXOPYRROLIDINE-1,2-DICARBOXYLATE is used as a potential pharmaceutical compound for its unique molecular structure and functional groups. Its application in this industry is due to the possibility of its interaction with biological systems and potential therapeutic effects, which require further research and development to fully understand and exploit.
(Note: Since the provided materials do not specify any particular applications or industries for (2S,4S)-1-TERT-BUTYL 2-METHYL 4-BENZYL-5-OXOPYRROLIDINE-1,2-DICARBOXYLATE, the use case listed above is a general assumption based on the mention of potential applications in pharmaceuticals or other industries. More specific applications would require additional information or research.)

Upstream product

• 100-39-0 benzyl bromide 
• 108963-96-8 (S)-1-tert-butoxycarbonyl-5-methoxycarbonyl-pyrrolidin-2-one 
• 24424-99-5 di-tert-butyl dicarbonate 
• 4931-66-2 methyl (S)-pyroglutamate 

Downstream Products

• 612820-04-9 (2S,4R,5S)-4-benzyl-5-cis-propenylpyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester 
• 612820-11-8 (2S,4R,5S)-5-allyl-4-benzylpyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester 
• 612820-16-3 (2S,4R,5S)-5-allyl-4-benzyl-1-but-3-enoylpyrrolidine-2-carboxylic acid methyl ester 
• 612820-06-1 (2S,4R,5S)-4-benzyl-1-but-3-enoyl-5-cis-propenylpyrrolidine-2-carboxylic acid methyl ester 
• 612820-14-1 (2S,4R,5S)-1-acryloyl-5-allyl-4-benzylpyrrolidine-2-carboxylic acid methyl ester 
• 612820-08-3 (1R,3S,9S)-1-benzyl-5-oxo-1,2,3,5,6,8a-hexahydroindolizine-3-carboxylic acid methyl ester 
• 129446-70-4 (2S,4R)-2-amino-4-benzyl pentanedioic acid 

Relevant articles and documents

Monatin, its stereoisomers and derivatives: Modeling the sweet taste chemoreception mechanism

The sweet natural compound monatin 1 has two stereogenic centers, and the 2S,4S absolute configuration has been attributed previously to the natural isomer. Among the four stereoisomers of monatin, three of them, particularly the 2R,4R isomer, tastes intensely sweet. The conformations of the four compounds have been studied by means of molecular modelling techniques. Both the diastereoisomeric forms show strong intramolecular hydrogen bonds which involve different functional groups and give rise to two different minimum energy conformations. The tertiary alcohol group in monatin seems to be indirectly involved in the generation of the taste, acting as an important contraint in generating the active conformation. The most important glucophores have been identified in the terminal -NH3+ and -COO - groups and in the indole ring by comparison with known topological models of sweet compounds and through the synthesis of appropriate derivatives in which some of these groups are lacking or modified. The relative affinity of each stereoisomer for its putative sweet taste receptor has been estimated semi-quantitatively with the pseudoreceptor modelling technique. The predicted activity calculated with this technique is in good agreement with the experimental data and explains why the 2R,4R isomer (and not the natural 2S,4S isomer) is the sweetest of the series. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2005.

Synthesis of diversely functionalized indolizidinones and related bicyclic lactams using intramolecular Grubbs olefin metathesis and Dieckmann condensation

Bicyclic 1-aza-2-oxo ring systems with versatile functionality were synthesized from the Grubbs olefin metathesis of appropriate olefinic precursors, starting with L-pyroglutamic acid. The carbocyclization products were further functionalized utilizing th