4-(三氟甲基)苯酚

  • ≥97%
有货

库存信息

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库存信息

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库存信息

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库存信息

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库存信息

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货号 (SKU) 包装规格 是否现货 价格 数量
T106656-1g
1g 现货 Stock Image
T106656-5g
5g 现货 Stock Image
T106656-10g
10g 现货 Stock Image
T106656-25g
25g 现货 Stock Image
T106656-100g
100g 期货 Stock Image

基本描述

别名 对三氟甲基苯酚,α,α,α-三氟对甲酚
英文别名 .ALPHA.,.ALPHA.,.ALPHA.-TRIFLUORO-4-CRESOL | 4-Trifluoromethylphenol | 4-trifluoromethyl-phenol | AC-2562 | NSC88303 | NSC-88303 | 4-Hydroxybenzotrifluoride | 4-hydroxybenzotri-fluoride | AS-8193 | BP-12755 | EINECS 206-945-7 | MLPXZYNPCSAQFS-UHFFFAOYSA-N
规格或纯度 ≥97%
英文名称 4-(Trifluoromethyl)phenol
储存温度 2-8°C储存,充氩
运输条件 冰袋运输
产品介绍

4-(三氟甲基)苯酚分子,与 H61T(HIS-61→苏氨酸)突变体的活性位点结合,密度较强。4-(Trifluoromethyl)phenol (4-hydroxybenzotrifluoride) was used in the synthesis of diaryl ether

4-(Trifluoromethyl)phenol molecule, bound at the active site of H61T (His-61→Thr) mutant, shows strong density.
4-(Trifluoromethyl)phenol (4-hydroxybenzotrifluoride) was used in the synthesis of diaryl ether

AI解读

关联靶点(人)

MIA PaCa-2 (5949 活性数据)
活性类型 Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

关联靶点(其它种属)

ethR HTH-type transcriptional regulator EthR (94 活性数据)
活性类型 Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

作用机制

作用机制 Action Type target ID Target Name Target Type Target Organism Binding Site Name 参考文献

名称和识别符

EC号 206-945-7
分子类型 小分子
IUPAC Name 4-(trifluoromethyl)phenol
INCHI InChI=1S/C7H5F3O/c8-7(9,10)5-1-3-6(11)4-2-5/h1-4,11H
InChi Key BAYGVMXZJBFEMB-UHFFFAOYSA-N
Canonical SMILES C1=CC(=CC=C1C(F)(F)F)O
Isomeric SMILES C1=CC(=CC=C1C(F)(F)F)O
WGK Germany 3
PubChem CID 67874
分子量 162.11
Beilstein号 1637019
Reaxy-Rn 1637019

化学和物理性质

溶解性 不溶于水;可溶于甲醇
敏感性 热及湿度敏感
闪点(℉) 183.2 °F
闪点(℃) 84℃
沸点 71.5-72°C
熔点 46°C
分子量 162.110 g/mol
XLogP3 2.800
氢键供体数Hydrogen Bond Donor Count 1
氢键受体数Hydrogen Bond Acceptor Count 4
可旋转键计数Rotatable Bond Count 0
精确质量Exact Mass 162.029 Da
单同位素质量Monoisotopic Mass 162.029 Da
拓扑极表面积Topological Polar Surface Area 20.200 Ų
重原子数Heavy Atom Count 11
形式电荷Formal Charge 0
复杂度Complexity 124.000
同位素原子数Isotope Atom Count 0
定义的原子立体中心计数Defined Atom Stereocenter Count 0
未定义的原子立体中心计数Undefined Atom Stereocenter Count 0
定义的键立体中心计数Defined Bond Stereocenter Count 0
未定义的键立体中心计数Undefined Bond Stereocenter Count 0
所有立体化学键的总数The total count of all stereochemical bonds 0
共价键合单元计数Covalently-Bonded Unit Count 1

安全和危险性(GHS)

象形图 GHS06,   GHS05,   GHS07,   GHS02
信号词 Danger
危险声明

H315: 引起皮肤刺激

H335: 可能引起呼吸道刺激

H301: 吞咽会中毒

H318: 造成严重的眼睛损伤

H228: 易燃固体

预防措施声明

P261: 避免吸入灰尘/烟雾/气体/雾/蒸汽/喷雾

P280: 戴防护手套/穿防护服/戴防护眼罩/戴防护面具。

P370+P378: 火灾时:使用干砂、干粉或抗醇泡沫灭火。

P210: 远离热源,热表面,火花,明火和其他点火源。 - 禁止抽烟。

P302+P352: 如皮肤沾染:用水充分清洗。

P321: 特殊处理(请参阅此标签上的...)。

P405: 密闭存放

P501: 将内容物/容器处理到。。。

P240: 地面/粘结容器和接收设备

P264: 处理后要彻底洗手。

P271: 仅在室外或通风良好的地方使用。

P241: 使用防爆的[电气/通风/照明/.../]设备。

P270: 使用本产品时,请勿进食、饮水或吸烟。

P304+P340: 如误吸入:将人转移到空气新鲜处,保持呼吸舒适体位。

P403+P233: 存放在通风良好的地方。保持容器密闭。

P362+P364: 脱掉沾污的衣服,清洗后方可重新使用。

P330: 漱口

P264+P265: 处理后彻底洗手[和…]。不要触摸眼睛。

P301+P316: 如果吞咽:立即寻求紧急医疗救助。

P305+P354+P338: 如果进入眼睛:立即用水冲洗几分钟。取下隐形眼镜(如果有的话),并且操作简单。继续冲洗。

P317: 寻求紧急医疗救助。

P332+P317: 如果出现皮肤刺激:请寻求医疗帮助。

P319: 如果你感到不适,请寻求医疗帮助。

WGK Germany 3
Reaxy-Rn 1637019
个人防护装备 dust mask type N95 (US),Eyeshields,Faceshields,Gloves

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找到12个结果

批号(Lot Number) 证书类型 日期 货号
G2321284 分析证书 25-04-07 T106656
G2321416 分析证书 25-04-07 T106656
G2321974 分析证书 25-04-07 T106656
H2204167 分析证书 24-05-07 T106656
H2204180 分析证书 24-05-07 T106656
G2416239 分析证书 24-04-02 T106656
K2422247 分析证书 23-05-17 T106656
F2129398 分析证书 23-04-12 T106656
F2129396 分析证书 23-04-12 T106656
H2204178 分析证书 22-06-18 T106656
H2204179 分析证书 22-06-18 T106656
H1816103 分析证书 22-04-27 T106656

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此产品的引用文献

1. Chun-rong Zhu, Jia-ping Xie, Hong-rong Mou, Zhen-jie Huang, Qian Tang, Cheng-bin Gong, Xiang-kai Fu.  (2019)  Dual-colored 4,4′,4′′,4′′′-(cyclobutane-1,2,3,4-tetrayl)-tetrabenzoate electrochromic materials with large optical contrast and coloration efficiency.  NEW JOURNAL OF CHEMISTRY,  43  (34): (13654-13661).  [10.1039/C9NJ03352A]

参考文献

1. D C Thompson,K Perera,R London.  (2000-05-29)  Spontaneous hydrolysis of 4-trifluoromethylphenol to a quinone methide and subsequent protein alkylation..  Chemico-biological interactions,  126  ((1)): (1-14).  [PMID:10826650]
2. M W Fraaije,R H van Den Heuvel,W J van Berkel,A Mattevi.  (2000-09-14)  Structural analysis of flavinylation in vanillyl-alcohol oxidase..  The Journal of biological chemistry,  275  ((49)): (38654-38658).  [PMID:10984479]
3. Zhao-Qian Liu,Zhi-Rong Tan,Dan Wang,Song-Lin Huang,Lian-Sheng Wang,Hong-Hao Zhou.  (2002-05-09)  Simultaneous determination of fluoxetine and its metabolite p-trifluoromethylphenol in human liver microsomes using a gas chromatographic-electron-capture detection procedure..  Journal of chromatography. B, Analytical technologies in the biomedical and life sciences,  769  ((2)): (305-311).  [PMID:11996496]
4. Yang Tian,Dae-Hwan Suk,Feng Cai,David Crich,Andrew D Mesecar.  (2008-11-01)  Bacillus anthracis o-succinylbenzoyl-CoA synthetase: reaction kinetics and a novel inhibitor mimicking its reaction intermediate..  Biochemistry,  47  ((47)): (12434-12447).  [PMID:18973344]
5. Przemysław Drzewicz,Agata Drobniewska,Katarzyna Sikorska,Grzegorz Nałęcz-Jawecki.  (2018-05-15)  Analytical and ecotoxicological studies on degradation of fluoxetine and fluvoxamine by potassium ferrate..  Environmental technology,  40  ((25)): (3265-3275).  [PMID:29756529]
6. Jordi Quintana,Alejandra Hernández,Francesc Ventura,Ricard Devesa,Maria Rosa Boleda.  (2019-04-11)  Identification of 3-(trifluoromethyl)phenol as the malodorous compound in a pollution incident in the water supply in Catalonia (N.E. Spain)..  Environmental science and pollution research international,  26  ((16)): (16076-16084).  [PMID:30968295]
7. Lisa Bauer,Roberto Manganaro,Birgit Zonsics,Jeroen R P M Strating,Priscila El Kazzi,Moira Lorenzo Lopez,Rachel Ulferts,Clara van Hoey,Maria J Maté,Thierry Langer,Bruno Coutard,Andrea Brancale,Frank J M van Kuppeveld.  (2019-07-16)  Fluoxetine Inhibits Enterovirus Replication by Targeting the Viral 2C Protein in a Stereospecific Manner..  ACS infectious diseases,  ((9)): (1609-1623).  [PMID:31305993]
8. L J Urichuk,L J Aspeslet,A Holt,P H Silverstone,R T Coutts,G B Baker.  (1997-11-21)  Determination of p-trifluoromethylphenol, a metabolite of fluoxetine, in tissues and body fluids using an electron-capture gas chromatographic procedure..  Journal of chromatography. B, Biomedical sciences and applications,  698  ((1-2)): (103-109).  [PMID:9367198]
9. Jin-Kyun Lee,Matthew J Fuchter,Rachel M Williamson,Gary A Leeke,Edward J Bush,Ian F McConvey,Simon Saubern,John H Ryan,Andrew B Holmes.  (2008-10-03)  Diaryl ether synthesis in supercritical carbon dioxide in batch and continuous flow modes..  Chemical communications (Cambridge, England),  (39)  ((39)): (4780-4782).  [PMID:18830491]
10. B van de Wier,J M Balk,A Bast,G H Koek,G R M M Haenen.  (2015-10-03)  Chemical characteristics for optimizing CYP2E1 inhibition..  Chemico-biological interactions,  242  (139-144).  [PMID:26428356]
11. Selina Tisler,Florian Zindler,Finnian Freeling,Karsten Nödler,László Toelgyesi,Thomas Braunbeck,Christian Zwiener.  (2019-05-29)  Transformation Products of Fluoxetine Formed by Photodegradation in Water and Biodegradation in Zebrafish Embryos ( Danio rerio)..  Environmental science & technology,  53  ((13)): (7400-7409).  [PMID:31136157]
12. Chun-rong Zhu, Jia-ping Xie, Hong-rong Mou, Zhen-jie Huang, Qian Tang, Cheng-bin Gong, Xiang-kai Fu.  (2019)  Dual-colored 4,4′,4′′,4′′′-(cyclobutane-1,2,3,4-tetrayl)-tetrabenzoate electrochromic materials with large optical contrast and coloration efficiency.  NEW JOURNAL OF CHEMISTRY,  43  (34): (13654-13661).  [10.1039/C9NJ03352A]

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