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Merck
CN

559792

Sigma-Aldrich

3-(3,5-二氯苯基)-N-(1-甲基乙基)-2,4-二氧代-1-咪唑烷羧酰胺

97%

别名:

异菌脲

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About This Item

线性分子式:
Cl2C6H3N2C3H2O2CONHCH(CH3)2
CAS号:
分子量:
330.17
Beilstein:
895003
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

方案

97%

mp

130-134 °C (lit.)

官能团

amine
chloro

SMILES字符串

CC(C)NC(=O)N1CC(=O)N(C1=O)c2cc(Cl)cc(Cl)c2

InChI

1S/C13H13Cl2N3O3/c1-7(2)16-12(20)17-6-11(19)18(13(17)21)10-4-8(14)3-9(15)5-10/h3-5,7H,6H2,1-2H3,(H,16,20)

InChI key

ONUFESLQCSAYKA-UHFFFAOYSA-N

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象形图

Health hazardEnvironment

警示用语:

Warning

危险声明

危险分类

Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges

法规信息

新产品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Chad R Blystone et al.
Toxicological sciences : an official journal of the Society of Toxicology, 111(1), 179-188 (2009-07-01)
Vinclozolin and iprodione are dicarboximide fungicides that display antiandrogenic effects in the male rat, which suggests that a mixture would lead to cumulative effects on androgen-sensitive end points. Iprodione is a steroid synthesis inhibitor, but androgen receptor antagonist activity, which
Chad R Blystone et al.
Toxicology letters, 174(1-3), 74-81 (2007-10-13)
Iprodione (IPRO) is a dichlorophenyl dicarboximide fungicide similar to procymidone and vinclozolin. All three of these fungicides induce Leydig cell tumors in the rat testis in long-term studies and an endocrine mode of action has been hypothesized to mediate this
Renáta Húsková et al.
Journal of chromatography. A, 1216(35), 6326-6334 (2009-08-01)
A combination of fast GC with narrow-bore column and bench top quadrupole mass spectrometer (MS) detector in negative chemical ionization (NCI) mode (with methane as reagent gas) is set up and utilized for the ultratrace analysis of 25 selected pesticides.
Abul K M Anisuzzaman et al.
Journal of agricultural and food chemistry, 56(2), 502-506 (2007-12-21)
Both primary and secondary alcohols degrade iprodione, 3-(3,5-dichlorophenyl)-N-(1-methylethyl)-2,4-dioxo-1-imidazolidine carboxamide. Steric hindrance has been found to have an inverse effect on the rate of its decomposition, and a fully substituted alcohol, such as tert-butanol, does not degrade iprodione due to extreme
Leiyan Yan et al.
Fungal genetics and biology : FG & B, 47(9), 753-760 (2010-07-03)
We present a characterization of bos5 from Botrytis cinerea, a gene that encodes a mitogen-activated protein kinase kinase (MAPKK), which is homologous to OS-5 of Neurospora crassa. The bos5 gene deletion mutant exhibited reduced vegetative growth and strongly impaired conidiation.

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