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2-咪唑烷酮

2-咪唑烷酮结构式
2-咪唑烷酮结构式
品牌特惠专场
常用名 2-咪唑烷酮 英文名 2-Imidazolidinone
CAS号 120-93-4 分子量 86.092
密度 1.1±0.1 g/cm3 沸点 358.7±11.0 °C at 760 mmHg
分子式 C3H6N2O 熔点 129-132 °C(lit.)
MSDS 美版 闪点 202.5±19.4 °C
符号 GHS07
GHS07
信号词 Warning

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.

J. Phys. Chem. A 114(34) , 9237-45, (2010)

A computational study of the structural and thermochemical properties of N-phenyl (open) and N-alkyl (cyclic) ureas, through the use of M05-2X and B3LYP density functional theory calculations has been carried out. The consistency of the literature experimenta...

Synthesis of new unsymmetrical 4,5-dihydroxy-2-imidazolidinones. Dynamic NMR spectroscopic study of the prototropic tautomerism in 1-(2-benzimidazolyl)-3-phenyl-4,5-dihydroxy-2-imidazolidinone.

Molecules 11(10) , 768-75, (2006)

The acid-catalyzed cyclocondensation in refluxing acetonitrile of aqueous glyoxal with N-heteroaryl-N'-phenylureas 4a-f (heteroaryl = 2-thiazolyl, 2-pyrimidinyl,2-pyrazinyl, 2-pyridinyl, 3-pyridinyl and 2-benzimidazolyl) led to the formation of the correspond...

[Preliminary pharmacological evaluation of new imidazolidinone-2, ethylenediamine and imidazoline derivatives].

Acta Pol. Pharm. 41(4) , 495-504, (1984)

Exploration of a series of 5-arylidene-2-thioxoimidazolidin-4-ones as inhibitors of the cytolytic protein perforin.

J. Med. Chem. 56(23) , 9542-55, (2013)

A series of novel 5-arylidene-2-thioxoimidazolidin-4-ones were investigated as inhibitors of the lymphocyte-expressed pore-forming protein perforin. Structure-activity relationships were explored through variation of an isoindolinone or 3,4-dihydroisoquinolin...

[Synthesis and structural study of 5-arylidene thiazolidine-2,4-diones and 3-substituted-4-thio-imidazolidine-2-ones].

Ann. Pharm. Fr. 53(5) , 209-14, (1995)

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. T...

[Pharmacologic studies of new derivatives of imidazoline, 2-imidazolidinone and imidazolidine-2-thione].

Acta Pol. Pharm. 43(2) , 180-8, (1986)

[Pharmacological studies of the central effects of new ethylguanidine, imidazolidine and imidazolidinone-2 derivatives].

Acta Pol. Pharm. 44(1) , 107-15, (1987)

[Polyadenylate polymerase in the diagnosis of the early stages of chemical carcinogenesis].

Gig. Tr. Prof. Zabol. (2) , 25-8, (1988)

Difference in teratogenic potency of ethylenethiourea in rats and mice: relative contribution of embryonic and maternal factors.

Teratology 40(6) , 555-66, (1989)

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. This study was undertake...

Rational design of novel, potent piperazinone and imidazolidinone BACE1 inhibitors.

Bioorg. Med. Chem. Lett. 18(11) , 3236-41, (2008)

Guided by structure-based design, we synthesized two novel series of potent inhibitors of BACE1 and generated extensive SAR around both the prime and non-prime side binding pockets. The key feature of both series is a cyclic amine motif specifically crafted t...