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31534

Supelco

2-Imidazolidone

PESTANAL®, analytical standard

Sinonimo/i:

N,N′-Ethyleneurea

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About This Item

Formula empirica (notazione di Hill):
C3H6N2O
Numero CAS:
120-93-4
Peso molecolare:
86.09
Beilstein:
106252
Numero CE:
204-436-4
Numero MDL:
MFCD00005257
Codice UNSPSC:
41116107
ID PubChem:
329753801
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

100

Nome Commerciale

PESTANAL®

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

Punto di fusione

129-132 °C (lit.)

applicazioni

agriculture
environmental

Formato

neat

Stringa SMILE

O=C1NCCN1

InChI

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

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Descrizione generale

Find more information here: Neonicotinoids

Applicazioni

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Prodotti consigliati

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Note legali

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

Pittogrammi

Health hazardExclamation mark
GHS08,GHS07

Avvertenze

Warning

Indicazioni di pericolo

H319,H373

Classi di pericolo

Eye Irrit. 2 - STOT RE 2

Organi bersaglio

Thyroid

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

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Certificati d'analisi (COA)

Lot/Batch Number
BCCG0830
BCBT4902

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Alaa A-M Abdel-Aziz et al.
Bioorganic & medicinal chemistry letters, 22(5), 2008-2014 (2012-02-10)
Novel series of 1-(arenesulfonyl)imidazolidin-2-one (3a-i) and 1,3-bis(arenesulfonyl)imidazolidin-2-one (5a-i) have been synthesized and tested for their antitumor activity against 60 tumor cell lines taken from nine different organs. A significant inhibition for cancer cells was observed with series 5a-i compounds compared
Rafael Bautista et al.
The Journal of organic chemistry, 76(19), 7901-7911 (2011-08-17)
An efficient and versatile synthesis of novel exo-imidazolidin-2-one dienes is described. This involves the base-assisted condensation/cyclization cascade reaction of the monoimino derivatives of diacetyl with a series of isocyanates. This methodology enables preparation of symmetrical dienes, as long as the
[Preliminary pharmacological evaluation of new imidazolidinone-2, ethylenediamine and imidazoline derivatives].
E Jagiełło-Wójtowicz et al.
Acta poloniae pharmaceutica, 41(4), 495-504 (1984-01-01)
J F Albuquerque et al.
Annales pharmaceutiques francaises, 53(5), 209-214 (1995-01-01)
The synthesis and the physico-chemical properties of four 3-(4-bromophenacyl)-5-arylidene-thiazolidine-2,4-diones, two 3-(4-bromobenzyl)-5-arylidene-thiazolidine-2,4-diones and seven 3-(4-chlorobenzyl)-5-arylidene-4-thio-imidazolidine-2-ones were described. These products were synthetized by the aldolisation-crotonisation reaction between aromatic aldehydes and substituted thiazolidinediones or thio-imidazolidinones.
[Pharmacological studies of the central effects of new ethylguanidine, imidazolidine and imidazolidinone-2 derivatives].
I Zebrowska-Lupina et al.
Acta poloniae pharmaceutica, 44(1), 107-115 (1987-01-01)
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Recensioni

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