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I601

2-Imidazolidone

96%

Synonym(s):

2-Oxoimidazolidine, N,N′-Ethyleneurea

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25 g
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$63.60
500 g

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1 kg

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About This Item

Empirical Formula (Hill Notation):
C3H6N2O
CAS Number:
120-93-4
Molecular Weight:
86.09
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24896082
EC Number:
204-436-4
Beilstein/REAXYS Number:
106252
MDL number:
MFCD00005257
Assay:
96%

$63.60

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Quality Level

200

assay

96%

mp

129-132 °C (lit.)

SMILES string

O=C1NCCN1

InChI

1S/C3H6N2O/c6-3-4-1-2-5-3/h1-2H2,(H2,4,5,6)

InChI key

YAMHXTCMCPHKLN-UHFFFAOYSA-N

Gene Information

human ... EPHX2(2053)
mouse ... Ephx2(13850)

Application

Reactant for synthesis of:
  • Chiral microporous materials from achiral precursors[1]
  • Aryl and heteroaryl N-acylureas via microwave-assisted palladium-catalyzed carbonylation
  • A highly water-soluble peptide based human neutrophil elastase inhibitor[2]
  • Heterocycles by cyanoacetylation for antimicrobial use

Reactant for:
  • Pd-catalyzed C-N bond formation with heteroaromatic tosylates[3]
  • Oxidative amidation of activated alkenes

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8.04789M043100319856
2-Imidazolidone 96%

Sigma-Aldrich

I601

2-Imidazolidone

2-Imidazolidinone hemihydrate for synthesis

Sigma-Aldrich

8.04789

2-Imidazolidinone hemihydrate

6-Hexachloro-Fluorescein Phosphoramidite

Sigma-Aldrich

M043100

6-Hexachloro-Fluorescein Phosphoramidite

Acetophenone-(phenyl-d5) 99 atom % D

Sigma-Aldrich

319856

Acetophenone-(phenyl-d5)

assay

96%

assay

-

assay

≥97% (31P-NMR), ≥97.0% (reversed phase HPLC)

assay

99% (CP)

Quality Level

200

Quality Level

200

Quality Level

200

Quality Level

200

mp

129-132 °C (lit.)

mp

58 °C

mp

-

mp

19-20 °C (lit.)

Gene Information

human ... EPHX2(2053)
mouse ... Ephx2(13850)

Gene Information

-

Gene Information

-

Gene Information

-

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pictograms

Health hazardExclamation mark
GHS08,GHS07

target_organs

Thyroid

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

signalword

Danger

Hazard Classifications

ED HH 1 - Eye Irrit. 2 - Repr. 1B - STOT RE 2

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

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Certificates of Analysis (COA)

Lot/Batch Number
BCCM4746
BCCH3283
STBJ9951
STBJ7182
STBJ5452

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Mette L H Mantel et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 16(18), 5437-5442 (2010-04-09)
A protocol for the palladium(0)-catalyzed amidation of heteroaromatic tosylates was successfully developed. The methodology proved to be effective for a variety of heteroaryl tosylates including the pyridine, pyrimidine, quinoline and quinoxaline ring systems. Successful carbon-nitrogen bond formation with these heteroaryl
Synthesis and antimicrobial activity of new heterocycles obtained using cyanoacetylation
Sh. M. Abu-Bakr, et al.,
Pharmaceutical Chemistry Journal, 44, 433-437 (2010)
Yasunao Inoue et al.
Bioorganic & medicinal chemistry, 17(21), 7477-7486 (2009-10-09)
A series of peptide-based transition-state human neutrophil elastase (HNE) inhibitors with N-terminal acidic moieties were synthesized and their inhibitory activity against HNE was evaluated both in vitro and in vivo. Our results show that compounds containing cyclic amide bridged acidic
View All Related Papers

Global Trade Item Number

SKUGTIN
I601-500G04061833857656
I601-25G04061833327487
I601-1KG04061826718414

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