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线性分子式:
(CF3)2CFI
化学文摘社编号:
分子量:
295.93
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
211-643-3
Beilstein/REAXYS Number:
1841228
MDL number:
Assay:
98%
Form:
liquid
InChI key
BBZVTTKMXRPMHZ-UHFFFAOYSA-N
InChI
1S/C3F7I/c4-1(11,2(5,6)7)3(8,9)10
SMILES string
FC(F)(F)C(F)(I)C(F)(F)F
vapor pressure
7.12 psi ( 20 °C)
assay
98%
form
liquid
refractive index
n20/D 1.329 (lit.)
bp
40 °C (lit.)
density
2.08 g/mL at 25 °C (lit.)
functional group
fluoro, iodo
storage temp.
2-8°C
Quality Level
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General description
Heptafluoro-2-iodopropane is a secondary fluoro alkyl iodide. It can be prepared by addition of iodine monofluoride to hexafluoropropene.
Application
Heptafluoro-2-iodopropane may be used in the preparation of perfluoropropyl magnesium bromide and perfluoropropyl magnesium iodide. It may be used as chain-transfer agent in telomerization reactions of:
- 1,1-difluoroethylene and tetrafluoroethylene
- CF3I, C2F5I and n-C3F7I with 1,1-difluoroethylene
- n-C3F7I with tetrafluoroethylene
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Inhalation - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves
Telomerization reactions in the synthesis of models for some fluorocarbon Polymers.
Chambers RD, et al.
Tetrahedron, 20(3), 497-506 (1964)
372. Organometallic and metalloid compounds made from heptafluoro-2-iodopropane, and their properties.
Chambers RD, et al.
Journal of the Chemical Society, 1962, 1993-1999 null
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