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Merck
CN

736120

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 5 mm × 8 in., NMR tube wall thickness 0.24 mm , ultra-thin wall

别名:

三氟甲苯

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关于此项目

线性分子式:
C6H5CF3
化学文摘社编号:
分子量:
146.11
NACRES:
NA.24
PubChem Substance ID:
UNSPSC Code:
12142201
EC Number:
214-061-8
MDL number:
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InChI key

GETTZEONDQJALK-UHFFFAOYSA-N

InChI

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

SMILES string

FC(F)(F)c1ccccc1

grade

analytical standard

concentration

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

technique(s)

NMR: suitable

NMR tube size

5 mm × 8 in.

NMR tube wall thickness

0.24 mm , ultra-thin wall

suitability

suitable for NMR (reference standard)

format

single component solution

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Features and Benefits

19F 灵敏度

Preparation Note

5 mm O.D. tube contains 0.700 mL.

signalword

Danger

Hazard Classifications

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

target_organs

Blood

存储类别

3 - Flammable liquids

wgk

WGK 3

flash_point_f

12.2 °F

flash_point_c

-11 °C

法规信息

危险化学品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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.
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.
[Hygienic standardization of benzotrifluoride level in reservoir water].
V I Antonova et al.
Gigiena i sanitariia, (2)(2), 86-87 (1985-02-01)
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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