2-苯基-1,3-噻唑-4-甲酸

• 常用名: 2-苯基-1,3-噻唑-4-甲酸
• 英文名: 2-Phenylthiazole-4-carboxylic Acid
• CAS号: 7113-10-2
• 分子量: 205.233
• 密度: 1.4±0.1 g/cm3
• 沸点: 420.5±37.0 °C at 760 mmHg
• 分子式: C₁₀H₇NO₂S
• 熔点: 175-177°C
• 闪点: 208.1±26.5 °C

2-苯基-1,3-噻唑-4-甲酸名称

• 中文名: 2-苯基-1,3-噻唑-4-甲酸
• 英文名: 2-Phenylthiazole-4-carboxylic acid
• 中文别名: 2-苯基-1,3-噻唑-4-羧酸 | 2-苯基噻唑-4-羧酸

2-苯基-1,3-噻唑-4-甲酸物理化学性质

• 密度: 1.4±0.1 g/cm3
• 沸点: 420.5±37.0 °C at 760 mmHg
• 熔点: 175-177°C
• 分子式: C₁₀H₇NO₂S
• 分子量: 205.233
• 闪点: 208.1±26.5 °C
• 精确质量: 205.019745
• PSA: 78.43000
• LogP: 2.92
• InChIKey: IBUSLNJQKLZPNR-UHFFFAOYSA-N
• SMILES: O=C(O)c1csc(-c2ccccc2)n1
• 外观性状: 奶油色固体
• 蒸汽压: 0.0±1.0 mmHg at 25°C
• 折射率: 1.643
• 储存条件: 室温
• 分子结构:

  1、 摩尔折射率：54.25

  2、 摩尔体积（cm³/mol）：149.9

  3、 等张比容（90.2K）：420.0

  4、 表面张力（dyne/cm）：61.5

  5、 极化率（10-24cm3）：21.50

2-苯基-1,3-噻唑-4-甲酸MSDS

2-苯基-1,3-噻唑-4-甲酸MSDS英文版

2-苯基-1,3-噻唑-4-甲酸安全信息

• 危害码 (欧洲): Xi: Irritant;
• 风险声明 (欧洲): 36/37/38
• 安全声明 (欧洲): S26-S36/37/39
• 海关编码: 2934100090

2-苯基-1,3-噻唑-4-甲酸海关

• 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%

2-苯基-1,3-噻唑-4-甲酸靶点实验

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：Inhibition of recombinant Pseudomonas aeruginosa MBL IMP-1 using nitrocefin as substr... 来源：ChEMBL 靶标：Beta-lactamase External Id：CHEMBL2090106

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

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2-苯基-1,3-噻唑-4-甲酸英文别名

• 2-Phenyl-1,3-thiazole-4-carboxylic acid
• MFCD00141954
• 2-Phenylthiazole-4-carboxylic Acid