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5-氨基-1,3-二甲基-4-硝基吡唑

更新时间:2025-08-20 10:38:00

5-氨基-1,3-二甲基-4-硝基吡唑结构式
5-氨基-1,3-二甲基-4-硝基吡唑结构式
品牌特惠专场
常用名 5-氨基-1,3-二甲基-4-硝基吡唑 英文名 5-AMINO-1,3-DIMETHYL-4-NITROPYRAZOLE
CAS号 76689-64-0 分子量 156.14300
密度 1.55g/cm3 沸点 327.3ºC at 760 mmHg
分子式 C5H8N4O2 熔点 136-138ºC
MSDS N/A 闪点 151.8ºC

 5-氨基-1,3-二甲基-4-硝基吡唑名称

中文名 5-氨基-1,3-二甲基-4-硝基吡唑
英文名 2,5-dimethyl-4-nitropyrazol-3-amine
英文别名 更多

 5-氨基-1,3-二甲基-4-硝基吡唑物理化学性质

密度 1.55g/cm3
沸点 327.3ºC at 760 mmHg
熔点 136-138ºC
分子式 C5H8N4O2
分子量 156.14300
闪点 151.8ºC
精确质量 156.06500
PSA 89.66000
LogP 1.32330
InChIKey BSUSGJKEVOQESO-UHFFFAOYSA-N
SMILES Cc1nn(C)c(N)c1[N+](=O)[O-]
折射率 1.664

 5-氨基-1,3-二甲基-4-硝基吡唑安全信息

危害码 (欧洲) Xi
海关编码 2933199090

 5-氨基-1,3-二甲基-4-硝基吡唑合成线路

~97%

5-氨基-1,3-二甲基-4-硝基吡唑结构式

5-氨基-1,3-二甲基-4-硝基吡唑

76689-64-0

文献:Andreeva, M. A.; Bolotov, M. I.; Isaev, Sh. G.; Mushii, R. Ya.; Perevalov, V. P.; et al. J. Gen. Chem. USSR (Engl. Transl.), 1980 , vol. 50, # 9 p. 2116 - 2119,1714 - 1716

~86%

5-氨基-1,3-二甲基-4-硝基吡唑结构式

5-氨基-1,3-二甲基-4-硝基吡唑

76689-64-0

文献:Katritzky, Alan R.; Vakulenko, Anatoliy V.; Sivapackiam, Jothilingam; Draghici, Bogdan; Damavarapu, Reddy Synthesis, 2008 , # 5 p. 699 - 706

~80%

5-氨基-1,3-二甲基-4-硝基吡唑结构式

5-氨基-1,3-二甲基-4-硝基吡唑

76689-64-0

文献:Alberola; Antolin; Gonzalez; et al. Journal of Heterocyclic Chemistry, 1986 , vol. 23, # 4 p. 1035 - 1038

~69%

5-氨基-1,3-二甲基-4-硝基吡唑结构式

5-氨基-1,3-二甲基-4-硝基吡唑

76689-64-0

文献:Alberola; Antolin; Gonzalez; et al. Journal of Heterocyclic Chemistry, 1986 , vol. 23, # 4 p. 1035 - 1038

~%

5-氨基-1,3-二甲基-4-硝基吡唑结构式

5-氨基-1,3-二甲基-4-硝基吡唑

76689-64-0

文献:J. Gen. Chem. USSR (Engl. Transl.), , vol. 50, # 9 p. 2116 - 2119,1714 - 1716

~%

5-氨基-1,3-二甲基-4-硝基吡唑结构式

5-氨基-1,3-二甲基-4-硝基吡唑

76689-64-0

文献:J. Gen. Chem. USSR (Engl. Transl.), , vol. 50, # 9 p. 2116 - 2119,1714 - 1716

~%

5-氨基-1,3-二甲基-4-硝基吡唑结构式

5-氨基-1,3-二甲基-4-硝基吡唑

76689-64-0

文献:J. Gen. Chem. USSR (Engl. Transl.), , vol. 50, # 9 p. 2116 - 2119,1714 - 1716

~%

5-氨基-1,3-二甲基-4-硝基吡唑结构式

5-氨基-1,3-二甲基-4-硝基吡唑

76689-64-0

文献:Chemistry of Heterocyclic Compounds (New York, NY, United States), , vol. 20, # 12 p. 1397 Khimiya Geterotsiklicheskikh Soedinenii, , # 12 p. 1691 - 1692

 5-氨基-1,3-二甲基-4-硝基吡唑海关

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%

 5-氨基-1,3-二甲基-4-硝基吡唑靶点实验

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: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: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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 5-氨基-1,3-二甲基-4-硝基吡唑英文别名

5-amino-1,3-dimethyl-4-nitro-1H-pyrazole
5-AMINO-1,3-DIMETHYL-4-NITROPYRAZOLE
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