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3(4-溴苯)-1H-5-氨基吡唑

更新时间:2025-08-25 14:42:06

3(4-溴苯)-1H-5-氨基吡唑结构式
3(4-溴苯)-1H-5-氨基吡唑结构式
品牌特惠专场
常用名 3(4-溴苯)-1H-5-氨基吡唑 英文名 5-(4-bromophenyl)-2H-pyrazol-3-ylamine
CAS号 78583-82-1 分子量 238.08400
密度 1.645g/cm3 沸点 485.1ºC at 760 mmHg
分子式 C9H8BrN3 熔点 172-176ºC(lit.)
MSDS 中文版 美版 闪点 247.2ºC
符号 GHS05 GHS07
GHS05, GHS07
信号词 Danger

 3(4-溴苯)-1H-5-氨基吡唑名称

中文名 5-氨基-3-(4-溴苯基)-1H-吡唑
英文名 5-(4-bromophenyl)-1H-pyrazol-3-amine
中文别名 5-(4-溴苯)-2H-3-氨基吡唑
英文别名 更多

 3(4-溴苯)-1H-5-氨基吡唑物理化学性质

密度 1.645g/cm3
沸点 485.1ºC at 760 mmHg
熔点 172-176ºC(lit.)
分子式 C9H8BrN3
分子量 238.08400
闪点 247.2ºC
精确质量 236.99000
PSA 54.70000
LogP 3.00260
InChIKey FTCWIBNIYIEHDT-UHFFFAOYSA-N
SMILES Nc1cc(-c2ccc(Br)cc2)[nH]n1
折射率 1.689
储存条件 2-8°C

 3(4-溴苯)-1H-5-氨基吡唑MSDS

 3(4-溴苯)-1H-5-氨基吡唑安全信息

符号 GHS05 GHS07
GHS05, GHS07
信号词 Danger
危害声明 H302-H315-H318-H335
警示性声明 P261-P280-P305 + P351 + P338
个人防护装备 dust mask type N95 (US);Eyeshields;Faceshields;Gloves
危害码 (欧洲) Xn: Harmful;Xi: Irritant;
风险声明 (欧洲) R22
安全声明 (欧洲) 26-36
危险品运输编码 NONH for all modes of transport
WGK德国 3
海关编码 2933199090

 3(4-溴苯)-1H-5-氨基吡唑合成线路

~65%

3(4-溴苯)-1H-5-氨基吡唑结构式

3(4-溴苯)-1H-5-氨基吡唑

78583-82-1

文献:Hartmann, Horst; Liebscher, Juergen Synthesis, 1984 , # 3 p. 276 - 277

~%

3(4-溴苯)-1H-5-氨基吡唑结构式

3(4-溴苯)-1H-5-氨基吡唑

78583-82-1

文献:Bioorganic and Medicinal Chemistry Letters, , vol. 20, # 3 p. 922 - 926

 3(4-溴苯)-1H-5-氨基吡唑上下游产品

3(4-溴苯)-1H-5-氨基吡唑上游产品  2

3(4-溴苯)-1H-5-氨基吡唑下游产品  1

 3(4-溴苯)-1H-5-氨基吡唑海关

海关编码 2933199090
中文概述 2933199090. 其他结构上有非稠合吡唑环化合物. 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, 乌洛托品请注明外观, 6-己内酰胺请注明外观, 签约日期
Summary 2933199090. other compounds containing an unfused pyrazole ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 3(4-溴苯)-1H-5-氨基吡唑靶点实验

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: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: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:qHTS of TDP-43 Inhibitors: NCGC Sytravon Library Screen
来源:NCGC
External Id:tdp43-p2-repeat
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
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 3(4-溴苯)-1H-5-氨基吡唑英文别名

MFCD00558911
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