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Merck
CN

468517

3,5-双(三氟甲基)苯基异硫氰酸酯

98%

别名:

1-异硫氰酸基-3,5-双(三氟甲基)苯

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关于此项目

线性分子式:
(CF3)2C6H3NCS
化学文摘社编号:
分子量:
271.18
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
98%
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Quality Level

assay

98%

refractive index

n20/D 1.5 (lit.)

bp

63 °C/1.5 mmHg (lit.)

density

1.485 g/mL at 25 °C (lit.)

functional group

fluoro, isothiocyanate

SMILES string

FC(F)(F)c1cc(cc(c1)C(F)(F)F)N=C=S

InChI

1S/C9H3F6NS/c10-8(11,12)5-1-6(9(13,14)15)3-7(2-5)16-4-17/h1-3H

InChI key

FXOSSGVJGGNASE-UHFFFAOYSA-N

Application

3,5-双(三氟甲基)苯基异硫氰酸酯已用于以下研究:
  • 氨基官能化模型表面的化学衍生化,金上的氨基硫醇盐,硅上的氨基硅氧烷,以及聚乙烯(PE)箔和膜。
  • ω-氨基-4,4′-三联苯基取代的链烷硫醇的自组装单层的化学衍生化。
  • 乙烯基磺酰亚胺硫脲的合成。
  • 吡咯烷-2-羧酸-{2- [3-(3,5-双三氟甲基苯基)硫脲基]苯基}-酰胺的制备。


pictograms

Skull and crossbones

signalword

Danger

Hazard Classifications

Acute Tox. 3 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

228.2 °F - closed cup

flash_point_c

109 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Highly diastereo-and enantioselective direct aldol reactions promoted by water-compatible organocatalysts bearing a pyrrolidinyl-camphor structural scaffold.
Tzeng Z-H, et al.
Tetrahedron, 65(5), 2879-2888 (2009)
Paul M Dietrich et al.
Langmuir : the ACS journal of surfaces and colloids, 26(6), 3949-3954 (2010-01-01)
Amino-terminated self-assembled monolayers on gold substrates were studied by X-ray photoelectron spectroscopy (XPS), near-edge X-ray absorption fine structure (NEXAFS) measurements, and atomic force microscopy (AFM). Two different omega-amino-4,4'-terphenyl substituted alkanethiols of the general structure H(2)N-(C(6)H(4))(3)-(CH(2))(n)-SH (ATPn) were used: 2-(4''-amino-1,1':4',1''-terphenyl-4-yl)ethane-1-thiol (n
Marcus Frings et al.
Beilstein journal of organic chemistry, 8, 1443-1451 (2012-09-29)
For the first time, chiral sulfoximine derivatives have been applied as asymmetric organocatalysts. In combination with a thiourea-type backbone the sulfonimidoyl moiety leads to organocatalysts showing good reactivity in the catalytic desymmetrization of a cyclic meso-anhydride and moderate enantioselectivity in



全球贸易项目编号

货号GTIN
468517-1G04061837804113
468517-5G04061832358567