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4-溴-1-甲基-1H-吡唑-3-羧酸

更新时间:2025-08-25 12:27:02

4-溴-1-甲基-1H-吡唑-3-羧酸结构式
4-溴-1-甲基-1H-吡唑-3-羧酸结构式
品牌特惠专场
常用名 4-溴-1-甲基-1H-吡唑-3-羧酸 英文名 4-bromo-1-methyl-1H-pyrazole-3-carboxylic acid
CAS号 84547-86-4 分子量 205.00900
密度 1.93 沸点 347.4ºC at 760 mmHg
分子式 C5H5BrN2O2 熔点 211-213ºC
MSDS 美版 闪点 163.9ºC

 4-溴-1-甲基-1H-吡唑-3-羧酸名称

中文名 4-溴-1-甲基-1H-吡唑-3-羧酸
英文名 4-Bromo-1-methyl-1H-pyrazole-3-carboxylic acid
中文别名 1-甲基-4-溴吡唑-3-甲酸
英文别名 更多

 4-溴-1-甲基-1H-吡唑-3-羧酸物理化学性质

密度 1.93
沸点 347.4ºC at 760 mmHg
熔点 211-213ºC
分子式 C5H5BrN2O2
分子量 205.00900
闪点 163.9ºC
精确质量 203.95300
PSA 55.12000
LogP 0.88080
InChIKey LEEPGDCCHVRYHK-UHFFFAOYSA-N
SMILES Cn1cc(Br)c(C(=O)O)n1
储存条件 2-8°C,干燥密封

 4-溴-1-甲基-1H-吡唑-3-羧酸安全信息

危害码 (欧洲) Xi: Irritant;
风险声明 (欧洲) R22;R36/37/38
安全声明 (欧洲) 22-26-36/37/39
海关编码 2933199090

 4-溴-1-甲基-1H-吡唑-3-羧酸合成线路

~22%

4-溴-1-甲基-1H-吡唑-3-羧酸结构式

4-溴-1-甲基-1H-吡唑-3-羧酸

84547-86-4

文献:Manaev, Yu. A.; Andreeva, M. A.; Perevalov, V. P.; Stepanov, B. I.; Dubrovskaya, V. A.; Seraya, V. I. J. Gen. Chem. USSR (Engl. Transl.), 1982 , vol. 52, # 11 p. 2592 - 2598,2291 - 2296

~28%

4-溴-1-甲基-1H-吡唑-3-羧酸结构式

4-溴-1-甲基-1H-吡唑-3-羧酸

84547-86-4

文献:Manaev, Yu. A.; Andreeva, M. A.; Perevalov, V. P.; Stepanov, B. I.; Dubrovskaya, V. A.; Seraya, V. I. J. Gen. Chem. USSR (Engl. Transl.), 1982 , vol. 52, # 11 p. 2592 - 2598,2291 - 2296

~%

4-溴-1-甲基-1H-吡唑-3-羧酸结构式

4-溴-1-甲基-1H-吡唑-3-羧酸

84547-86-4

文献:J. Gen. Chem. USSR (Engl. Transl.), , vol. 52, # 11 p. 2592 - 2598,2291 - 2296

 4-溴-1-甲基-1H-吡唑-3-羧酸海关

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%

 4-溴-1-甲基-1H-吡唑-3-羧酸靶点实验

查看更多实验

实验名称:Discovery of Small Molecules to Inhibit Human Cytomegalovirus Nuclear Egress
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:HCMV UL50
External Id:HMS1262
实验名称:High-throughput screen for inhibitors of the GIV GBA-motif interaction with Galpha-i ...
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id:HMS1303
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:Alphascreen assay for small molecules abrogating mHTT-CaM Interaction
来源:24983
靶标:Huntingtin
External Id:KUHTS-Muma KU-CaM-Htt INH-01
实验名称:Cell-based high throughput primary assay to identify activators of GPR151
来源:The Scripps Research Institute Molecular Screening Center
靶标:RecName: Full=G-protein coupled receptor 151; AltName: Full=G-protein coupled receptor PGR7; AltName: Full=GPCR-2037; AltName: Full=Galanin receptor 4; AltName: Full=Galanin-receptor-like protein; Short=GalRL
External Id:GPR151_PHUNTER_AG_LUMI_1536_1X%ACT
实验名称:AlphaScreen-based biochemical high throughput primary assay to identify activators of...
来源:The Scripps Research Institute Molecular Screening Center
靶标:N/A
External Id:FBW7_ACT_ALPHA_1536_1X%ACT PRUN
实验名称:AlphaScreen-based biochemical high throughput primary assay to identify inhibitors of...
来源:The Scripps Research Institute Molecular Screening Center
External Id:MITF_INH_Alpha_1536_1X%INH PRUN
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 4-溴-1-甲基-1H-吡唑-3-羧酸英文别名

MFCD00463988
4-bromo-1-methylpyrazole-3-carboxylic acid
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