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4-(5-苯基-1,3,4-噁二唑)苯甲酸

更新时间:2025-08-25 09:45:32

4-(5-苯基-1,3,4-噁二唑)苯甲酸结构式
4-(5-苯基-1,3,4-噁二唑)苯甲酸结构式
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常用名 4-(5-苯基-1,3,4-噁二唑)苯甲酸 英文名 4-(5-Phenyl-1,3,4-oxadiazol-2-yl)benzoic acid
CAS号 85292-45-1 分子量 266.25200
密度 1.319g/cm3 沸点 484.3ºC at 760 mmHg
分子式 C15H10N2O3 熔点 N/A
MSDS N/A 闪点 246.7ºC

 4-(5-苯基-1,3,4-噁二唑)苯甲酸名称

中文名 4-(5-苯基-1,3,4-噁二唑)苯甲酸
英文名 4-(5-Phenyl-1,3,4-oxadiazol-2-yl)benzoic acid
英文别名 更多

 4-(5-苯基-1,3,4-噁二唑)苯甲酸物理化学性质

密度 1.319g/cm3
沸点 484.3ºC at 760 mmHg
分子式 C15H10N2O3
分子量 266.25200
闪点 246.7ºC
精确质量 266.06900
PSA 76.22000
LogP 3.10180
InChIKey KJSLGQIRTJNTKD-UHFFFAOYSA-N
SMILES O=C(O)c1ccc(-c2nnc(-c3ccccc3)o2)cc1
折射率 1.619

 4-(5-苯基-1,3,4-噁二唑)苯甲酸安全信息

海关编码 2934999090

 4-(5-苯基-1,3,4-噁二唑)苯甲酸合成线路

~86%

4-(5-苯基-1,3,4-噁二唑)苯甲酸结构式

4-(5-苯基-1,3,4-噁...

85292-45-1

文献:Takeda Chemical Industries, Ltd. Patent: EP1405636 A1, 2004 ;

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4-(5-苯基-1,3,4-噁二唑)苯甲酸结构式

4-(5-苯基-1,3,4-噁...

85292-45-1

文献:Grekow,A.P.; Schvaika,O.P. J. Gen. Chem. USSR (Engl. Transl.), 1960 , vol. 30, p. 3802 - 3806,3763 - 3766

~%

4-(5-苯基-1,3,4-噁二唑)苯甲酸结构式

4-(5-苯基-1,3,4-噁...

85292-45-1

文献:Huisgen,R. et al. Chemische Berichte, 1960 , vol. 93, p. 2106 - 2124

~%

4-(5-苯基-1,3,4-噁二唑)苯甲酸结构式

4-(5-苯基-1,3,4-噁...

85292-45-1

文献:Huisgen,R. et al. Chemische Berichte, 1960 , vol. 93, p. 2106 - 2124

 4-(5-苯基-1,3,4-噁二唑)苯甲酸上下游产品

4-(5-苯基-1,3,4-噁二唑)苯甲酸上游产品  3

4-(5-苯基-1,3,4-噁二唑)苯甲酸下游产品  2

 4-(5-苯基-1,3,4-噁二唑)苯甲酸海关

海关编码 2934999090
中文概述 2934999090. 其他杂环化合物. 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
Summary 2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 4-(5-苯基-1,3,4-噁二唑)苯甲酸靶点实验

查看更多实验

实验名称:C. difficile toxins: Counterscreen in absence of substrate UDPG Measured in Biochemic...
来源:Broad Institute
靶标:N/A
External Id:7074-02_Inhibitor_Dose_CherryPick_Activity
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: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:Dicer-mediated maturation of pre-microRNA
来源:Center for Chemical Genomics, University of Michigan
靶标:N/A
External Id:TargetID_659_CEMA
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 4-(5-苯基-1,3,4-噁二唑)苯甲酸英文别名

HMS2873O19
2-Phenyl-5-(4-carboxy-phenyl)-1,3,4-oxadiazol
4-(5-phenyl-[1,3,4]oxadiazol-2-yl)-benzoic acid
2-Phenyl-5-(4-carboxy-phenyl)-1,3,4-oxdiazol
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