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5-对甲基苯基-2-氨基-1,3,4-噻二唑

更新时间:2025-08-27 12:47:36

5-对甲基苯基-2-氨基-1,3,4-噻二唑结构式
5-对甲基苯基-2-氨基-1,3,4-噻二唑结构式
品牌特惠专场
常用名 5-对甲基苯基-2-氨基-1,3,4-噻二唑 英文名 5-(p-Tolyl)-1,3,4-thiadiazol-2-amine
CAS号 26907-54-0 分子量 191.253
密度 1.3±0.1 g/cm3 沸点 364.9±35.0 °C at 760 mmHg
分子式 C9H9N3S 熔点 218-222ºC
MSDS N/A 闪点 174.5±25.9 °C

 5-对甲基苯基-2-氨基-1,3,4-噻二唑名称

中文名 5-对甲基苯基-2-氨基-1,3,4-噻二唑
英文名 5-(4-methylphenyl)-1,3,4-thiadiazol-2-amine
中文别名 2-氨基-5-(4-甲基苯基)-1,3,4-噻二唑 | 2-氨基-5-(4-甲氧苯基)-1,3,4-噻二唑
英文别名 更多

 5-对甲基苯基-2-氨基-1,3,4-噻二唑物理化学性质

密度 1.3±0.1 g/cm3
沸点 364.9±35.0 °C at 760 mmHg
熔点 218-222ºC
分子式 C9H9N3S
分子量 191.253
闪点 174.5±25.9 °C
精确质量 191.051712
PSA 80.04000
LogP 2.49
InChIKey ZLDPCNCAFSBFCX-UHFFFAOYSA-N
SMILES Cc1ccc(-c2nnc(N)s2)cc1
蒸汽压 0.0±0.8 mmHg at 25°C
折射率 1.651
储存条件 2-8°C,避光,保存于惰性气体中

 5-对甲基苯基-2-氨基-1,3,4-噻二唑MSDS

 5-对甲基苯基-2-氨基-1,3,4-噻二唑安全信息

危害码 (欧洲) Xn: Harmful;
风险声明 (欧洲) 22-36/37/38
安全声明 (欧洲) 26
海关编码 2934999090

 5-对甲基苯基-2-氨基-1,3,4-噻二唑合成线路

~89%

5-对甲基苯基-2-氨基-1,3,4-噻二唑结构式

5-对甲基苯基-2-氨基-1,...

26907-54-0

文献:Tu, GuoGang; Li, ShaoHua; Huang, HuiMing; Li, Gang; Xiong, Fang; Mai, Xi; Zhu, HuaWei; Kuang, BinHai; Xu, Wen Fang Bioorganic and Medicinal Chemistry, 2008 , vol. 16, # 14 p. 6663 - 6668

~77%

5-对甲基苯基-2-氨基-1,3,4-噻二唑结构式

5-对甲基苯基-2-氨基-1,...

26907-54-0

文献:Rajak, Harish; Agarawal, Avantika; Parmar, Poonam; Thakur, Bhupendra Singh; Veerasamy, Ravichandran; Sharma, Prabodh Chander; Kharya, Murli Dhar Bioorganic and Medicinal Chemistry Letters, 2011 , vol. 21, # 19 p. 5735 - 5738

~56%

5-对甲基苯基-2-氨基-1,3,4-噻二唑结构式

5-对甲基苯基-2-氨基-1,...

26907-54-0

文献:Jain, Sanmati K.; Mishra, Pradeep Asian Journal of Chemistry, 2011 , vol. 23, # 3 p. 1305 - 1308

~67%

5-对甲基苯基-2-氨基-1,3,4-噻二唑结构式

5-对甲基苯基-2-氨基-1,...

26907-54-0

文献:Malbec, Frederique; Milcent, Rene; Barbier, Geo Journal of Heterocyclic Chemistry, 1984 , vol. 21, p. 1689 - 1698

~%

5-对甲基苯基-2-氨基-1,3,4-噻二唑结构式

5-对甲基苯基-2-氨基-1,...

26907-54-0

文献:Mishra, Pradeep; Jatav, Varsha; Kashaw Journal of the Indian Chemical Society, 2006 , vol. 83, # 11 p. 1165 - 1170

~%

5-对甲基苯基-2-氨基-1,3,4-噻二唑结构式

5-对甲基苯基-2-氨基-1,...

26907-54-0

文献:Malbec, Frederique; Milcent, Rene; Barbier, Geo Journal of Heterocyclic Chemistry, 1984 , vol. 21, p. 1689 - 1698

 5-对甲基苯基-2-氨基-1,3,4-噻二唑海关

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%

 5-对甲基苯基-2-氨基-1,3,4-噻二唑靶点实验

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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 5-对甲基苯基-2-氨基-1,3,4-噻二唑英文别名

5-(4-Methylphenyl)-1,3,4-thiadiazol-2-amine
2-Amino-5-(4-methylphenyl)-1,3,4-thiadiazole
T5NN DSJ CZ ER D1
5-p-Tolyl-[1,3,4]thiadiazol-2-ylamine
5-(p-Tolyl)-1,3,4-thiadiazol-2-amine
5-(4-methylphenyl)-1,3,4-thiadiazole-2-ylamine
2-Amino-5-(p-tolyl)-1,3,4-thiadiazole
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