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366706

Sigma-Aldrich

3,5-双(三氟甲基)碘苯

98%

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5 G
CN¥281.31

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5 G
CN¥281.31

About This Item

线性分子式:
(CF3)2C6H3I
CAS Number:
分子量:
340.00
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

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质量水平

方案

98%

表单

liquid

折射率

n20/D 1.463 (lit.)

沸点

59-61 °C/10 mmHg (lit.)

密度

1.919 g/mL at 25 °C (lit.)

SMILES字符串

FC(F)(F)c1cc(I)cc(c1)C(F)(F)F

InChI

1S/C8H3F6I/c9-7(10,11)4-1-5(8(12,13)14)3-6(15)2-4/h1-3H

InChI key

VDPIZIZDKPFXLI-UHFFFAOYSA-N

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此商品
23213015230438782
assay

98%

assay

97%

assay

≥95.0% (AT)

assay

97%

Quality Level

100

Quality Level

200

Quality Level

200

Quality Level

100

form

liquid

form

solid

form

solid

form

liquid

density

1.919 g/mL at 25 °C (lit.)

density

-

density

-

density

1.691 g/mL at 25 °C (lit.)

bp

59-61 °C/10 mmHg (lit.)

bp

-

bp

-

bp

146-147 °C (lit.)

refractive index

n20/D 1.463 (lit.)

refractive index

-

refractive index

-

refractive index

n20/D >1.4340 (lit.)

一般描述

1-Iodo-3,5-bis(trifluoromethyl)benzene is a halogenated hydrocarbon.

应用

1-Iodo-3,5-bis(trifluoromethyl)benzene may be used in the preparation of [bis(trifluoroacetoxy)iodo]perfluoroalkanes.[1] It may be used to investigate the fragmentation reactions of (E)- and (Z)-2-methylbuten-1-yl(aryl)iodonium triflates (aryl = C6H5-, 4-(CF3)C6H4, 3,5-(CF3)2C6H4-).[2]

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

10 - Combustible liquids

WGK

WGK 3

闪点(°F)

165.2 °F - closed cup

闪点(°C)

74 °C - closed cup

个人防护装备

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

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    Aleksandra A Zagulyaeva et al.
    The Journal of organic chemistry, 75(6), 2119-2122 (2010-02-19)
    [Bis(trifluoroacetoxy)iodo]perfluoroalkanes C(n)F(2n+1)I(OCOCF(3))(2) (n = 4, 6, 8, 10, 12) can be conveniently prepared by the oxidation of the corresponding perfluoroalkyl iodides with Oxone in trifluoroacetic acid at room temperature and subsequently converted to the stable [hydroxy(tosyloxy)iodo]perfluoroalkanes, C(n)F(2n+1)I(OH)OTs, by treatment with
    Fragmentations of (E)-and (Z)-isomers of 2-methylbuten-1-yl (aryl) iodonium triflates: competing mechanisms for enol triflate formation.
    Hinkle RJ.
    ARKIVOC (Gainesville, FL, United States), 6, 201-212 (2003)

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