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Merck
CN

733806

Sigma-Aldrich

α,α,α-三氟甲苯 溶液

suitable for NMR (reference standard), 0.05% in benzene-d6 (99.6 atom % D), NMR tube size 10 mm × 8 in.

别名:

三氟甲苯

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关于此项目

线性分子式:
C6H5CF3
CAS Number:
分子量:
146.11
EC 号:
MDL编号:
UNSPSC代码:
12142201
PubChem化学物质编号:
NACRES:
NA.12
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表单

solution

质量水平

浓度

0.05% in benzene-d6 (99.6 atom % D)

技术

NMR: suitable

NMR管尺寸

10 mm × 8 in.

适用性

suitable for NMR (reference standard)

SMILES字符串

FC(F)(F)c1ccccc1

InChI

1S/C7H5F3/c8-7(9,10)6-4-2-1-3-5-6/h1-5H

InChI key

GETTZEONDQJALK-UHFFFAOYSA-N

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特点和优势

19F 灵敏度

制备说明

10 mm O.D. tube contains 3.175 mL.

警示用语:

Danger

危险分类

Aquatic Chronic 3 - Asp. Tox. 1 - Carc. 1A - Eye Irrit. 2 - Flam. Liq. 2 - Muta. 1B - Skin Irrit. 2 - STOT RE 1

靶器官

Blood

储存分类代码

3 - Flammable liquids

WGK

WGK 3

闪点(°F)

12.2 °F

闪点(°C)

-11 °C

法规信息

新产品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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K H Engesser et al.
Applied microbiology and biotechnology, 32(5), 600-608 (1990-02-01)
Sixteen bacterial strains capable of degrading alkylbenzenes and alkylphenols were directly isolated from soil and water. The degradation pathways are discussed. Alkylcatechols are almost exclusively cleaved via meta-ring fission. Meta-cleavage of 3-trifluoromethyl-(TFM)-catechol was observed with all strains at different rates
Hidetoshi Yamada et al.
Carbohydrate research, 337(7), 581-585 (2002-03-23)
A glycosylation reaction induced by copper(II) trifluoromethanesulfonate is described. Using benzotrifluoride as the reaction solvent, five kinds of glycosyl donors, a glucosyl chloride, a fluoride, a trichloroacetimidate, a 1-O-acetyl compound, and a lactol were activated to give the corresponding glucosides.
Bhawani Singh Rathore et al.
Bioorganic & medicinal chemistry, 14(16), 5678-5682 (2006-05-03)
7-Chloro-5-trifluoromethyl/7-fluoro/7-trifluoromethyl-4H-1,4-benzothiazines have been synthesized by 2-amino-5-fluoro/5-trifluoromethyl/5-chloro-3-trifluoromethyl benzenethiols condensed with beta-diketone/beta-ketoesters in the presence of DMSO involving oxidative cyclization. Pharmacological activities have also been included.
Shota Tsukada et al.
Neuropharmacology, 48(4), 479-491 (2005-03-10)
Glutamate transporters rapidly take up synaptically released glutamate and maintain the glutamate concentration in the synaptic cleft at a low level. (2S, 3S)-3-[3-[4-(trifluoromethyl)benzoylamino]benzyloxy]aspartate (TFB-TBOA) is a novel glutamate transporter blocker that potently suppresses the activity of glial transporters. TFB-TBOA inhibited
Eun Jin Cho et al.
Science (New York, N.Y.), 328(5986), 1679-1681 (2010-06-26)
The trifluoromethyl group can dramatically influence the properties of organic molecules, thereby increasing their applicability as pharmaceuticals, agrochemicals, or building blocks for organic materials. Despite the importance of this substituent, no general method exists for its installment onto functionalized aromatic

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