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Merck
CN

31534

2-咪唑烷酮

PESTANAL®, analytical standard

别名:

环乙烯脲

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经验公式（希尔记法）:
C3H6N2O
化学文摘社编号:
120-93-4
分子量:
86.09
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329753801
EC Number:
204-436-4
Beilstein/REAXYS Number:
106252
MDL number:
MFCD00005257

主要文件

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InChI key

YAMHXTCMCPHKLN-UHFFFAOYSA-N

InChI

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

SMILES string

O=C1NCCN1

grade

analytical standard

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

mp

129-132 °C (lit.)

application(s)

agriculture
environmental

format

neat

Quality Level

100

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General description

Find more information here: Neonicotinoids

Application

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

Other Notes

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.

Legal Information

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

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

存储类别

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

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
BCCG0830
BCBT4902

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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.
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
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
[Pharmacologic studies of new derivatives of imidazoline, 2-imidazolidinone and imidazolidine-2-thione].
I Zebrowska-Lupina et al.
Acta poloniae pharmaceutica, 43(2), 180-188 (1986-01-01)
G P Daston et al.
Teratology, 40(6), 555-566 (1989-12-01)
Ethylenethiourea (ETU) is a potent teratogen in the rat but not in the mouse or any other species tested. Embryotoxic and teratogenic effects are produced in mice only after exposure to 10-40 times the teratogenic dose of ETU in rats.
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实验方案

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