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BARBITURIC ACID, 5-CYCLOHEXYL-1,3-DIMETHYL

更新时间:2025-09-21 18:52:27

BARBITURIC ACID, 5-CYCLOHEXYL-1,3-DIMETHYL结构式
BARBITURIC ACID, 5-CYCLOHEXYL-1,3-DIMETHYL结构式
委托求购
常用名 BARBITURIC ACID, 5-CYCLOHEXYL-1,3-DIMETHYL 英文名 BARBITURIC ACID, 5-CYCLOHEXYL-1,3-DIMETHYL
CAS号 7391-65-3 分子量 238.28300
密度 1.202g/cm3 沸点 335.5ºC at 760 mmHg
分子式 C12H18N2O3 熔点 N/A
MSDS N/A 闪点 138.2ºC

 名称

英文名 5-cyclohexyl-1,3-dimethyl-1,3-diazinane-2,4,6-trione
英文别名 更多

 物理化学性质

密度 1.202g/cm3
沸点 335.5ºC at 760 mmHg
分子式 C12H18N2O3
分子量 238.28300
闪点 138.2ºC
精确质量 238.13200
PSA 57.69000
LogP 1.10910
折射率 1.528

 毒性和生态

 安全信息

海关编码 2933540000

 合成线路

~10%

BARBITURIC ACID, 5-CYCLOHEXYL-1,3-DIMETHYL结构式

BARBITURIC ACID...

7391-65-3

文献:Ramachary, Dhevalapally B.; Kishor, Mamillapalli; Reddy, Y. Vijayendar European Journal of Organic Chemistry, 2008 , # 6 p. 975 - 993

~%

BARBITURIC ACID, 5-CYCLOHEXYL-1,3-DIMETHYL结构式

BARBITURIC ACID...

7391-65-3

文献:Cope et al. Journal of the American Chemical Society, 1941 , vol. 63, p. 356

 海关

海关编码 2933540000
中文概述 2933540000 其他丙二酰脲(巴比土酸)的衍生物以及它们的盐。监管条件:无。增值税率:17.0%。退税率:9.0%。最惠国关税:6.5%。普通关税:20.0%
申报要素 品名, 成分含量, 用途, 乌洛托品请注明外观, 6-己内酰胺请注明外观, 签约日期
Summary 2933540000 other derivatives of malonylurea (barbituric acid); salts thereof。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:6.5%。General tariff:20.0%

 靶点实验

查看更多实验

实验名称:Luminescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:mu-type opioid receptor isoform MOR-1 [Homo sapiens]
External Id:OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN
实验名称:QFRET-based biochemical primary high throughput screening assay to identify exosite i...
来源:The Scripps Research Institute Molecular Screening Center
靶标:disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens]
External Id:ADAM17_INH_QFRET_1536_1X%INH PRUN
实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_AG_FLUO8_1536_1X%ACT PRUN
实验名称:qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
来源:NCGC
靶标:TDP1 protein [Homo sapiens]
External Id:TDP1100
实验名称:qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
来源:NCGC
靶标:TDP1 protein [Homo sapiens]
External Id:TDP1101
实验名称:Schnurri-3 Inhibitors: specific inducers of adult bone formation Measured in Cell-Bas...
来源:Broad Institute
靶标:N/A
External Id:2134-01_Inhibitor_SinglePoint_HTS_Activity_Set2
实验名称:Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
来源:Broad Institute
靶标:FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id:2147-01_Inhibitor_SinglePoint_HTS_Activity
实验名称:Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfect...
来源:Broad Institute
靶标:N/A
External Id:Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfected HEK293 cells Inhibition - 7011-01_Antagonist_SinglePoint_HTS_Activity
实验名称:Primary Screen Inhibitors of CD40 Signaling in BL2 Cells Measured in Cell-Based Syste...
来源:Broad Institute
靶标:N/A
External Id:7124-01_Inhibitor_SinglePoint_HTS_Activity
实验名称:qHTS for Inhibitors of AMA1-RON; Towards Development of Antimalarial Drug Lead: Prima...
来源:NCGC
靶标:apical membrane antigen 1, AMA1 [Plasmodium falciparum 3D7]
External Id:AMA1100
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 英文别名

BARBITURIC ACID,5-CYCLOHEXYL-1,3-DIMETHYL
5-Cyclohexyl-1,3-dimethyl-barbitursaeure
5-cyclohexyl-1,3-dimethylpyrimidine-2,4,6-trione
5-cyclohexyl-1,3-dimethyl-barbituric acid
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