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N,4-diphenylpiperazine-1-carboxamide

更新时间:2025-09-21 17:52:08

N,4-diphenylpiperazine-1-carboxamide结构式
N,4-diphenylpiperazine-1-carboxamide结构式
委托求购
常用名 N,4-diphenylpiperazine-1-carboxamide 英文名 N,4-diphenylpiperazine-1-carboxamide
CAS号 4791-20-2 分子量 281.35200
密度 1.216g/cm3 沸点 511.7ºC at 760 mmHg
分子式 C17H19N3O 熔点 N/A
MSDS N/A 闪点 263.3ºC

 N,4-diphenylpiperazine-1-carboxamide名称

英文名 N,4-diphenylpiperazine-1-carboxamide
英文别名 更多

 N,4-diphenylpiperazine-1-carboxamide物理化学性质

密度 1.216g/cm3
沸点 511.7ºC at 760 mmHg
分子式 C17H19N3O
分子量 281.35200
闪点 263.3ºC
精确质量 281.15300
PSA 35.58000
LogP 3.11660
InChIKey SAKOVSGMQXGABX-UHFFFAOYSA-N
SMILES O=C(Nc1ccccc1)N1CCN(c2ccccc2)CC1
折射率 1.644

 N,4-diphenylpiperazine-1-carboxamide安全信息

海关编码 2933599090

 N,4-diphenylpiperazine-1-carboxamide上下游产品

N,4-diphenylpiperazine-1-carboxamide上游产品  2

N,4-diphenylpiperazine-1-carboxamide下游产品  0

 N,4-diphenylpiperazine-1-carboxamide海关

海关编码 2933599090
中文概述 2933599090. 其他结构上有嘧啶环的化合物(包括其他结构上有哌嗪环的化合物. 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 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 2933599090. other compounds containing a pyrimidine ring (whether or not hydrogenated) or piperazine ring in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 N,4-diphenylpiperazine-1-carboxamide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:A screen for compounds that inhibit the activity of LtaS in Staphylococcus aureus
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id:HMS979
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:Fluorescence-based cell-based primary high throughput screening assay to identify pos...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_PAM_FLUO8_1536_1X%ACT PRUN
实验名称:Mycobacterium tuberculosis BioA enzyme inhibitor Measured in Biochemical System Using...
来源:Broad Institute
靶标:aspartate aminotransferase [Homo sapiens]
External Id:2163-07_Inhibitor_SinglePoint_DryPowder_Activity
实验名称:Fluorescence polarization-based biochemical high throughput primary assay to identify...
来源:The Scripps Research Institute Molecular Screening Center
靶标:RecName: Full=Sialate O-acetylesterase; AltName: Full=H-Lse; AltName: Full=Sialic acid-specific 9-O-acetylesterase; Flags: Precursor [Homo sapiens]
External Id:SIAE_INH_FP_1536_1X%INH PRUN
实验名称:uHTS identification of small molecule modulators of NR3A
来源:Burnham Center for Chemical Genomics
靶标:N/A
External Id:SBCCG-A1015-NR3A-Primary-Assay
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 N,4-diphenylpiperazine-1-carboxamide英文别名

1-piperazinecarboxamide,n,4-diphenyl
4-phenyl-piperazine-1-carboxylic acid anilide
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