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O-(4-联苯甲酰基)苯甲酸

更新时间:2025-10-10 14:37:20

O-(4-联苯甲酰基)苯甲酸结构式
O-(4-联苯甲酰基)苯甲酸结构式
品牌特惠专场
常用名 O-(4-联苯甲酰基)苯甲酸 英文名 2-(4-Biphenylylcarbonyl)benzoic acid
CAS号 42797-18-2 分子量 302.323
密度 1.2±0.1 g/cm3 沸点 539.3±43.0 °C at 760 mmHg
分子式 C20H14O3 熔点 225-227ºC
MSDS N/A 闪点 294.1±24.7 °C

 O-(4-联苯甲酰基)苯甲酸名称

中文名 O-(1,1’-二苯基-4-羰基)苯甲酸
英文名 O-(4-Biphenylylcarbonyl)Benzoic Acid
中文别名 O-(4-联苯甲酰基)苯甲酸 | o-(4-联苯羰基)苯甲酸 | 2-(4-联苯甲酰基)苯甲酸 | O-(1,1'-二苯基-4-羰基)苯甲酸 | 2-(4-联苯基羰基)苯甲酸
英文别名 更多

 O-(4-联苯甲酰基)苯甲酸物理化学性质

密度 1.2±0.1 g/cm3
沸点 539.3±43.0 °C at 760 mmHg
熔点 225-227ºC
分子式 C20H14O3
分子量 302.323
闪点 294.1±24.7 °C
精确质量 302.094299
PSA 54.37000
LogP 3.95
InChIKey NBYNVBRXIUUSIG-UHFFFAOYSA-N
SMILES O=C(O)c1ccccc1C(=O)c1ccc(-c2ccccc2)cc1
蒸汽压 0.0±1.5 mmHg at 25°C
折射率 1.632
储存条件 室温,干燥

 O-(4-联苯甲酰基)苯甲酸毒性和生态

 O-(4-联苯甲酰基)苯甲酸安全信息

海关编码 2918300090

 O-(4-联苯甲酰基)苯甲酸合成线路

~79%

O-(4-联苯甲酰基)苯甲酸结构式

O-(4-联苯甲酰基)苯甲酸

42797-18-2

文献:Guilhemat, Robert; Pereyre, Michel; Petraud, Michel Bulletin de la Societe Chimique de France, 1980 , vol. 2, # 7-8 p. 334 - 344

~55%

O-(4-联苯甲酰基)苯甲酸结构式

O-(4-联苯甲酰基)苯甲酸

42797-18-2

文献:Seo, Sangwon; Slater, Mark; Greaney, Michael F. Organic Letters, 2012 , vol. 14, # 10 p. 2650 - 2653

~%

O-(4-联苯甲酰基)苯甲酸结构式

O-(4-联苯甲酰基)苯甲酸

42797-18-2

文献:Koebrich,G.; Trapp,H. Chemische Berichte, 1968 , vol. 101, p. 2660 - 2664

~%

O-(4-联苯甲酰基)苯甲酸结构式

O-(4-联苯甲酰基)苯甲酸

42797-18-2

文献:Koebrich,G.; Trapp,H. Chemische Berichte, 1968 , vol. 101, p. 2660 - 2664

~%

O-(4-联苯甲酰基)苯甲酸结构式

O-(4-联苯甲酰基)苯甲酸

42797-18-2

文献:Elbs Journal fuer Praktische Chemie (Leipzig), 1890 , vol. <2> 41, p. 147

 O-(4-联苯甲酰基)苯甲酸海关

海关编码 2918300090
中文概述 2918300090 其他含醛基或酮基不含其他含氧基羧酸(包括酸酐、酰卤化物、过氧化物和过氧酸及该税号的衍生物). 增值税率:17.0% 退税率:9.0% 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 2918300090 other carboxylic acids with aldehyde or ketone function but without other oxygen function, their anhydrides, halides, peroxides, peroxyacids and their derivatives。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:6.5%。General tariff:30.0%

 O-(4-联苯甲酰基)苯甲酸靶点实验

查看更多实验

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:Inhibition of recombinant phosphatase activity of Cdc25B catalytic domain expressed i...
来源:ChEMBL
靶标:M-phase inducer phosphatase 2
External Id:CHEMBL2061093
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: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: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
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 O-(4-联苯甲酰基)苯甲酸英文别名

QVR BVR DR
o-(4-Biphenylylcarbonyl)benzoic acid
2-(4-Biphenylylcarbonyl)benzoic acid
2-(Biphenyl-4-ylcarbonyl)benzoic acid
2-{[1,1'-Biphenyl]-4-ylcarbonyl}benzoic acid
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