Skip to Content
Merck
CN

392308

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

98%

Synonym(s):

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

Sign In to View Organizational & Contract Pricing.

Select a Size

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%

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

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

SMILES string

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

InChI key

AYSUEIZKNBGWGN-VIFPVBQESA-N

assay

98%

optical activity

[α]24/D −63.0°, c = 2.5 in methanol

mp

189 °C (dec.) (lit.)

functional group

carboxylic acid, phenyl

Quality Level

100

Related Categories

Application

Z-protected imidazolidinone for sequential N-alkylation.

flash_point_c

Not applicable

pictograms

Exclamation mark
GHS07

signalword

Warning

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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
MKCV9158
MKBZ4828V
MKBX6890V
MKBJ3080V
74596KJ

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service