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(S)-3-Methyl-2-oxo-imidazolidine-1,5-dicarboxylic acid 1-benzyl ester 5-tert-butyl ester is a unique compound within the imidazolidine chemical class, characterized by a five-membered ring structure with two nitrogen atoms and three carbon atoms. One carbon atom in the ring is replaced by an oxygen atom, resulting in a 2-oxo-imidazolidine. The molecule features two carboxylic acid residues that form ester bonds with distinct groups: a benzyl group at the 1-position and a tert-butyl group at the 5-position. The benzyl group is a phenyl group attached to a CH2, while the tert-butyl group is an alkyl group with a central carbon bonded to three methyl groups. This specific arrangement of components gives rise to the distinctive structure of (S)-3-Methyl-2-oxo-imidazolidine-1,5-dicarboxylic acid 1-benzyl ester 5-tert-butyl ester.

83056-78-4

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83056-78-4 Usage

Uses

Used in Pharmaceutical Industry:
(S)-3-Methyl-2-oxo-imidazolidine-1,5-dicarboxylic acid 1-benzyl ester 5-tert-butyl ester is used as a potential pharmaceutical compound for its unique structural properties. The presence of the imidazolidine ring and the ester bonds with benzyl and tert-butyl groups may contribute to its potential as a therapeutic agent, possibly in the development of new drugs or as a component in drug delivery systems.
Used in Chemical Research:
(S)-3-Methyl-2-oxo-iMidazolidine-1,5-dicarboxylic acid 1-benzyl ester 5-tert-butyl ester is also used as a subject of study in chemical research, where its properties and reactivity can be explored. The specific arrangement of the benzyl and tert-butyl ester groups may offer insights into the synthesis of other complex molecules or the development of new chemical reactions and methodologies.
Used in Material Science:
(S)-3-Methyl-2-oxo-imidazolidine-1,5-dicarboxylic acid 1-benzyl ester 5-tert-butyl ester may be employed in material science applications, where its unique structure could be leveraged to create new materials with specific properties. (S)-3-Methyl-2-oxo-iMidazolidine-1,5-dicarboxylic acid 1-benzyl ester 5-tert-butyl ester's potential use in this field could include the development of novel polymers, coatings, or other advanced materials with tailored characteristics.

Check Digit Verification of cas no

The CAS Registry Mumber 83056-78-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,0,5 and 6 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 83056-78:
(7*8)+(6*3)+(5*0)+(4*5)+(3*6)+(2*7)+(1*8)=134
134 % 10 = 4
So 83056-78-4 is a valid CAS Registry Number.

83056-78-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl (4S)-3-(benzyloxycarbonyl)-1-methyl-2-oxoimidazolidine-4-carboxylate

1.2 Other means of identification

Product number -
Other names (S)-3-Methyl-2-oxo-imidazolidine-1,5-dicarboxylic acid 1-benzyl ester 5-tert-butyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:83056-78-4 SDS

83056-78-4Relevant academic research and scientific papers

Studies on Angiotensin Converting Enzyme Inhibitors. 4. Synthesis and Angiotensin Converting Enzyme Inhibitory Activities of 3-Acyl-1-alkyl-2-oxoimidazolidine-4-carboxylic Acid Derivatives

Hayashi, Kimiaki,Nunami, Ken-ichi,Kato, Jyoji,Yoneda, Naoto,Kubo, Masami,et al.

, p. 289 - 297 (2007/10/02)

(4S)-1-Alkyl-3-acyl>-2-oxoimidazolidine-4-carboxylic acid derivatives (3) were prepared by two methods.Their angiotensin converting enzyme (ACE) inhibitory activities and antihypertensive effects were evaluated, and the structure-activity relationships were discussed.The dicarboxylic acids 3a-n possessing S,S,S configuration showed potent in vitro ACE inhibitory activities with IC 50 values of 1.1x10-8-1.5x10-9 M.The most potent compound in this series, monoester 3p, had an ID 50 value of 0.24 mg/kg, po for inhibition of angiotensin I induced pressor response in normotensive rats and produced a dose-dependent decrease in systolic blood pressure of spontaneously hypertensive rats (SHRs) at doses of 1-10 mg/kg, po.

ANTIHYPERTENSIVE 2-OXO-IMIDAZOLIDINE DERIVATIVES

-

, (2008/06/13)

Novel 2-oxo-imidazolidine derivative of the formula: STR1 wherein R 1 is lower alkyl or phenyl-lower alkyl, R 2 is lower alkyl, R. sup.3 is alkyl of one to 12 carbon atoms or phenyl-lower alkyl and R 4 is hydrogen or lower alkyl, and a pharmaceutically acceptable salts thereof are disclsoed. Said compounds (I) and salts thereof are useful as hypotensive agents.

2-OXOIMIDAZOLIDINE DERIVATIVES

-

, (2008/06/13)

A 2-oxoimidazolidine derivative of the formula: STR1 wherein R 1 is lower alkyl or phenyl-lower alkyl and R 2 is lower alkyl or phenyl, and a process for preparation thereof are disclosed. Said 2-oxoimidazolidine derivative (I) or a pharmaceutically acceptable salt thereof is useful as a hypotensive agent.

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