(4-tert-butylphenyl) benzoate结构式
|
常用名 | (4-tert-butylphenyl) benzoate | 英文名 | (4-tert-butylphenyl) benzoate |
|---|---|---|---|---|
| CAS号 | 14041-81-7 | 分子量 | 254.32400 | |
| 密度 | 1.061g/cm3 | 沸点 | 357.4ºC at 760 mmHg | |
| 分子式 | C17H18O2 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 149.2ºC |
| 英文名 | 7,13,19,25-tetra-tert-butyl-27,28,29,30-tetrahydroxy-2,3-dihomo-3-oxacalix[4]arene |
|---|---|
| 英文别名 | 更多 |
| 密度 | 1.061g/cm3 |
|---|---|
| 沸点 | 357.4ºC at 760 mmHg |
| 分子式 | C17H18O2 |
| 分子量 | 254.32400 |
| 闪点 | 149.2ºC |
| 精确质量 | 254.13100 |
| PSA | 26.30000 |
| LogP | 4.20330 |
| InChIKey | OWZCLYMEMJOKAC-UHFFFAOYSA-N |
| SMILES | CC(C)(C)c1ccc(OC(=O)c2ccccc2)cc1 |
| 蒸汽压 | 2.73E-05mmHg at 25°C |
| 折射率 | 1.549 |
|
~96%
(4-tert-butylph... 14041-81-7 |
| 文献:Liu, Jianhua; Chen, Jing; Xia, Chungu Journal of Catalysis, 2008 , vol. 253, # 1 p. 50 - 56 |
|
~74%
(4-tert-butylph... 14041-81-7 |
| 文献:Wakita, Natsumi; Hara, Shoji Tetrahedron, 2010 , vol. 66, # 40 p. 7939 - 7945 |
|
~85%
(4-tert-butylph... 14041-81-7 |
| 文献:Chen, Guangwei; Leng, Yuting; Yang, Fan; Wang, Shiwei; Wu, Yangjie Chinese Journal of Chemistry, 2013 , vol. 31, # 12 p. 1488 - 1494 |
|
~%
(4-tert-butylph... 14041-81-7 |
| 文献:Studer Justus Liebigs Annalen der Chemie, 1882 , vol. 211, p. 246 |
|
~%
(4-tert-butylph... 14041-81-7 |
| 文献:Chen, Guangwei; Leng, Yuting; Yang, Fan; Wang, Shiwei; Wu, Yangjie Chinese Journal of Chemistry, 2013 , vol. 31, # 12 p. 1488 - 1494 |
|
~%
(4-tert-butylph... 14041-81-7 |
| 文献:Sears Journal of Organic Chemistry, 1948 , vol. 13, p. 120 |
|
~%
(4-tert-butylph... 14041-81-7 |
| 文献:Kamennov,N.A. et al. J. Appl. Chem. USSR (Engl. Transl.), 1967 , vol. 40, # 3 p. 643 - 647,624 - 627 |
|
~%
(4-tert-butylph... 14041-81-7 |
| 文献:Kreysler Chemische Berichte, 1885 , vol. 18, p. 1716 |
| (4-tert-butylphenyl) benzoate上游产品 9 | |
|---|---|
| (4-tert-butylphenyl) benzoate下游产品 4 | |
|
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
|
| p-tert-butylphenyl benzoate |
| 4-TERT-BUTYLCALIX(4)-CROWN-6 |
| 2,23,28,38-tetrakis(1,1-dimethylethyl)-6,7,9,10,12,13,15,16,18,19-decahydro-31H-4,21-(methano[1,3]benzenomethano)-26,30-metheno-25H-dibenzo[q,z][1,4,7,10,13,16]hexaoxacycloheptacosin-32,35-diol |
| p-tert-butylcalix[4]crown-6 |
| 7,13,19,25-tetra-tert-butyl-2,3-dihomo-3-oxacalix[4]arene |
| 4-Benzoyloxy-1-tert.-butyl-benzol |
| 4-tert-butylphenyl benzoate |
| p-tert-butyldihomooxacalix[4]arene |
| p-tert-butyldihomooxocalix[4]arene |
| (4-tert.-Butyl-phenyl)-benzoat |
| 5,11,17,23-tetrakis(1,1-dimethylethyl)-25,27-dihydroxycalix[4]arene-crown-6 |
| benzoic acid-(4-tert-butyl-phenyl ester) |
| Benzoesaeure-(4-tert-butyl-phenylester) |
| p-(t-butyl)phenyl benzoate |