120-93-4 | 2-Imidazolidone

Packsize	Purity	Availability	Price	Discounted Price
25g	98%	in stock	$6.00	$4.00
100g	98%	in stock	$9.00	$6.00

Description

• Catalog Number: AA33546
• Chemical Name: 2-Imidazolidone
• CAS Number: 120-93-4
• Molecular Formula: C3H6N2O
• Molecular Weight: 86.0925
• MDL Number: MFCD00149330
• SMILES: O=C1NCCN1

Computed Properties

• Complexity: 63.2
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 6
• Hydrogen Bond Acceptor Count: 1
• Hydrogen Bond Donor Count: 2
• XLogP3: -1.3

Literature

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  Chemical communications (Cambridge, England) 20121011

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  The Journal of organic chemistry 20111007

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• Computational thermochemistry of six ureas, imidazolidin-2-one, N,N'-trimethyleneurea, benzimidazolinone, parabanic acid, barbital (5,5'-diethylbarbituric acid), and 3,4,4'-trichlorocarbanilide, with an extension to related compounds.

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  Organic letters 20090618

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  The journal of physical chemistry. B 20090108

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  Journal of enzyme inhibition and medicinal chemistry 20081001

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  Bioorganic & medicinal chemistry letters 20080601

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  The Journal of organic chemistry 20070330

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  Molecules (Basel, Switzerland) 20061019

• A new synthesis of imidazolidin-2-ones via Pd-catalyzed carboamination of N-allylureas.

  Organic letters 20060608

• Potent inhibitors of the HIV-1 protease incorporating cyclic urea P1-P2 scaffold.

  Bioorganic & medicinal chemistry letters 20041115

• A two-unnatural-base-pair system toward the expansion of the genetic code.

  Journal of the American Chemical Society 20041020

• Dichlorobis(imidazolidin-2-one-kappaO)zinc(II) at 150 K.

  Acta crystallographica. Section C, Crystal structure communications 20031101

• Methyl 2-(2-chloroethylaminocarbonyl)diazenecarboxylate SB-166 inhibits the growth of different tumour cell lines, including drug-resistant sublines.

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  Parasite (Paris, France) 20021201

• Kinetics and mechanism for CO(2) scrambling in a N-carboxyimidazolidone analogue for N(1)-carboxybiotin.

  Journal of the American Chemical Society 20020925

• Further insight in the photochemistry of DNA: structure of a 2-imidazolone (5-4) pyrimidone adduct derived from the mutagenic pyrimidine (6-4) pyrimidone photolesion by UV irradiation.

  Journal of the American Chemical Society 20020320

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