1-苯基-3-丙基-2-硫脲结构式
|
常用名 | 1-苯基-3-丙基-2-硫脲 | 英文名 | Thiourea,N-phenyl-N'-propyl |
|---|---|---|---|---|
| CAS号 | 13140-47-1 | 分子量 | 194.29700 | |
| 密度 | 1.128g/cm3 | 沸点 | 282.1ºC at 760 mmHg | |
| 分子式 | C10H14N2S | 熔点 | 64-66ºC | |
| MSDS | N/A | 闪点 | 124.4ºC |
| 中文名 | 1-苯基-3-丙基-2-硫脲 |
|---|---|
| 英文名 | 1-Phenyl-3-propyl-2-thiourea |
| 英文别名 | 更多 |
| 密度 | 1.128g/cm3 |
|---|---|
| 沸点 | 282.1ºC at 760 mmHg |
| 熔点 | 64-66ºC |
| 分子式 | C10H14N2S |
| 分子量 | 194.29700 |
| 闪点 | 124.4ºC |
| 精确质量 | 194.08800 |
| PSA | 56.15000 |
| LogP | 2.84690 |
| InChIKey | HZPCVTKJHKWEDX-UHFFFAOYSA-N |
| SMILES | CCCNC(=S)Nc1ccccc1 |
| 外观性状 | 固体 |
| 蒸汽压 | 0.00343mmHg at 25°C |
| 折射率 | 1.621 |
| 储存条件 | 室温 |
| 计算化学 | 1.疏水参数计算参考值(XlogP):无 2.氢键供体数量:2 3.氢键受体数量:1 4.可旋转化学键数量:3 5.互变异构体数量:3 6.拓扑分子极性表面积:56.2 7.重原子数量:13 8.表面电荷:0 9.复杂度:153 10.同位素原子数量:0 11.确定原子立构中心数量:0 12.不确定原子立构中心数量:0 13.确定化学键立构中心数量:0 14.不确定化学键立构中心数量:0 15.共价键单元数量:1 |
| 危害码 (欧洲) | Xi |
|---|---|
| 海关编码 | 2930909090 |
| 1-苯基-3-丙基-2-硫脲上游产品 3 | |
|---|---|
| 1-苯基-3-丙基-2-硫脲下游产品 4 | |
| 海关编码 | 2930909090 |
|---|---|
| 中文概述 | 2930909090. 其他有机硫化合物. 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:30.0% |
| 申报要素 | 品名, 成分含量, 用途 |
| Summary | 2930909090. other organo-sulphur compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0% |
|
实验名称:Primary cell-based high-throughput screening assay for identification of compounds th...
来源:Johns Hopkins Ion Channel Center
靶标:regulator of G-protein signaling 4 isoform 2 [Homo sapiens]
External Id:JHICC_RGS_Act_HTS
|
|
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:uHTS identification of small molecule activators of the adaptive arm of the Unfolded ...
来源:Burnham Center for Chemical Genomics
靶标:N/A
External Id:BCCG-A405-UPR-XBP1-PrimaryAgonist-Assay
|
|
实验名称:Antibacterial activity against Klebsiella pneumoniae MDR ATCC 70063 (CO-ADD:GN_003); ...
来源:ChEMBL
靶标:Klebsiella pneumoniae
External Id:CHEMBL4296186
|
|
实验名称:High throughput fluorescence intensity-based biochemical assay to screen for small mo...
来源:University of Pittsburgh Molecular Library Screening Center
靶标:furin (paired basic amino acid cleaving enzyme), isoform CRA_a [Homo sapiens]
External Id:MH080376 Biochemical HTS for Inhibitors of the Proprotein Convertase Furin.
|
|
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:Identifying Sarm1 TIR NADase inhibitors through high throughput HPLC assay
来源:24386
靶标:N/A
External Id:Sarm1 TIR NADase inhibitors
|
| 1-PHENYL-3-PROPYL-2-THIOUREA |
| 1-phenyl-3-propylthiourea |