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392308

(S)-(−)-1-Z-2-Oxo-5-imidazolidinecarboxylic acid

Name: (<I>S</I>)-(−)-1-Z-2-Oxo-5-imidazolidinecarboxylic acid
Brand: ALDRICH

98%

Synonym(s):

(S)-(−)-2-Oxo-1,5-imidazolidinedicarboxylic acid 1-benzyl ester

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About This Item

Empirical Formula (Hill Notation):

C₁₂H₁₂N₂O₅

CAS Number:

59760-01-9

Molecular Weight:

264.23

NACRES:

NA.22

PubChem Substance ID:

24864442

UNSPSC Code:

12352005

MDL number:

MFCD00192373

Assay:

98%

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Properties

Quality Level

100

assay

98%

optical activity

[α]24/D −63.0°, c = 2.5 in methanol

mp

189 °C (dec.) (lit.)

functional group

carboxylic acid, phenyl

SMILES string

OC(=O)[C@@H]1CNC(=O)N1C(=O)OCc2ccccc2

InChI

1S/C12H12N2O5/c15-10(16)9-6-13-11(17)14(9)12(18)19-7-8-4-2-1-3-5-8/h1-5,9H,6-7H2,(H,13,17)(H,15,16)/t9-/m0/s1

InChI key

AYSUEIZKNBGWGN-VIFPVBQESA-N

Description

Application

Z-protected imidazolidinone for sequential N-alkylation.

flash_point_c

Not applicable

pictograms

GHS07

signalword

Warning

hcodes

H315,H319,H335

pcodes

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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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.

K Hayashi et al.

Journal of medicinal chemistry, 32(2), 289-297 (1989-02-01)

(4S)-1-Alkyl-3-[[N-(carboxyalkyl)amino]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

Global Trade Item Number

SKU	GTIN
392308-5G	04061832985787