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(4-甲基-2-噻唑)-苯胺

更新时间:2025-10-13 20:40:54

(4-甲基-2-噻唑)-苯胺结构式
(4-甲基-2-噻唑)-苯胺结构式
品牌特惠专场
常用名 (4-甲基-2-噻唑)-苯胺 英文名 2-Thiazolamine,4-methyl-N-phenyl
CAS号 90916-46-4 分子量 190.265
密度 1.2±0.1 g/cm3 沸点 316.2±35.0 °C at 760 mmHg
分子式 C10H10N2S 熔点 N/A
MSDS N/A 闪点 145.0±25.9 °C

 (4-甲基-2-噻唑)-苯胺名称

中文名 (4-甲基-2-噻唑)-苯胺
英文名 4-methyl-N-phenyl-1,3-thiazol-2-amine
中文别名 2-苯胺基-4-甲基噻唑 | 4-甲基-N-苯基-2-氨基噻唑
英文别名 更多

 (4-甲基-2-噻唑)-苯胺物理化学性质

密度 1.2±0.1 g/cm3
沸点 316.2±35.0 °C at 760 mmHg
分子式 C10H10N2S
分子量 190.265
闪点 145.0±25.9 °C
精确质量 190.056473
PSA 53.16000
LogP 2.79
InChIKey NTVCLKICUVTCND-UHFFFAOYSA-N
SMILES Cc1csc(Nc2ccccc2)n1
蒸汽压 0.0±0.7 mmHg at 25°C
折射率 1.659

 (4-甲基-2-噻唑)-苯胺安全信息

海关编码 2934100090

 (4-甲基-2-噻唑)-苯胺合成线路

~60%

(4-甲基-2-噻唑)-苯胺结构式

(4-甲基-2-噻唑)-苯胺

90916-46-4

文献:Oehler, Elisabeth; Kang, Heun-Soo; Zbiral, Erich Chemische Berichte, 1988 , vol. 121, p. 533 - 546

~%

(4-甲基-2-噻唑)-苯胺结构式

(4-甲基-2-噻唑)-苯胺

90916-46-4

文献:Oehler, Elisabeth; Kang, Heun-Soo; Zbiral, Erich Chemische Berichte, 1988 , vol. 121, p. 533 - 546

~%

(4-甲基-2-噻唑)-苯胺结构式

(4-甲基-2-噻唑)-苯胺

90916-46-4

文献:Traumann Justus Liebigs Annalen der Chemie, 1888 , vol. 249, p. 38

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(4-甲基-2-噻唑)-苯胺结构式

(4-甲基-2-噻唑)-苯胺

90916-46-4

文献:Sharma,G.M. et al. Tetrahedron, 1961 , vol. 15, p. 53 - 59

~%

(4-甲基-2-噻唑)-苯胺结构式

(4-甲基-2-噻唑)-苯胺

90916-46-4

文献:Murav'eva,K.M.; Shchukina,M.N. J. Gen. Chem. USSR (Engl. Transl.), 1960 , vol. 30, p. 2340 - 2343,2320 - 2323

~%

(4-甲基-2-噻唑)-苯胺结构式

(4-甲基-2-噻唑)-苯胺

90916-46-4

文献:Murav'eva,K.M.; Shchukina,M.N. J. Gen. Chem. USSR (Engl. Transl.), 1960 , vol. 30, p. 2340 - 2343,2320 - 2323

~%

(4-甲基-2-噻唑)-苯胺结构式

(4-甲基-2-噻唑)-苯胺

90916-46-4

文献:Schantl, Joachim G.; Lagoja, Irene M. Synthetic Communications, 1998 , vol. 28, # 8 p. 1451 - 1462

~%

(4-甲基-2-噻唑)-苯胺结构式

(4-甲基-2-噻唑)-苯胺

90916-46-4

文献:Hantzsch; Weber Chemische Berichte, 1887 , vol. 20, p. 3130

~%

(4-甲基-2-噻唑)-苯胺结构式

(4-甲基-2-噻唑)-苯胺

90916-46-4

文献:Bramley, (Miss) Susan E.; Dupplin, Viscount; Goberdhan, Dhanesh G. C.; Meakins, G. Denis Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1987 , p. 639 - 644

 (4-甲基-2-噻唑)-苯胺海关

海关编码 2934100090
中文概述 2934100090. 结构上含有一个非稠合噻唑环的化合物(不论是否氢化). 增值税率:17.0%. 退税率:9.0%. 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 2934100090 other compounds containing an unfused thiazole ring (whether or not hydrogenated) in the structure VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:20.0%

 (4-甲基-2-噻唑)-苯胺靶点实验

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: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: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: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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 (4-甲基-2-噻唑)-苯胺英文别名

4-Methyl-N-phenylthiazol-2-amine
4-methyl-2-phenylaminothiazole
(4-Methyl-thiazol-2-yl)-phenyl-amine
2-phenylamino-4-methyl-thiazole
4-Methyl-N-phenyl-2-thiazolamine
4-Methyl-N-phenyl-1,3-thiazol-2-amine
(4-Methyl-thiazol-2-yl)-phenyl-amin
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