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SMILES string
FC1(N(C=CN1c3c(cccc3C(C)C)C(C)C)c2c(cccc2C(C)C)C(C)C)F
InChI
1S/C27H36F2N2/c1-17(2)21-11-9-12-22(18(3)4)25(21)30-15-16-31(27(30,28)29)26-23(19(5)6)13-10-14-24(26)20(7)8/h9-20H,1-8H3
InChI key
FQXXWTOSPDVNSG-UHFFFAOYSA-N
form
liquid
concentration
0.1 M in toluene
density
0.865 g/mL at 25 °C
functional group
fluoro
storage temp.
2-8°C
Quality Level
Related Categories
1 of 4
This Item | |||
|---|---|---|---|
| form liquid | form solid | form liquid | form - |
| concentration 0.1 M in toluene | concentration - | concentration - | concentration - |
| density 0.865 g/mL at 25 °C | density 1.423 g/mL at 25 °C | density 1.423 g/mL at 25 °C | density 0.962 g/mL at 25 °C (lit.) |
| functional group fluoro | functional group - | functional group aldehyde, fluoro | functional group - |
| storage temp. 2-8°C | storage temp. - | storage temp. −20°C | storage temp. 2-8°C |
| Quality Level 100 | Quality Level - | Quality Level 100 | Quality Level - |
Application
Legal Information
related product
signalword
Danger
Hazard Classifications
Aquatic Chronic 3 - Asp. Tox. 1 - Flam. Liq. 2 - Repr. 2 - Skin Irrit. 2 - STOT RE 2 - STOT SE 3
target_organs
Central nervous system
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
39.2 °F
flash_point_c
4 °C
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Articles
PhenoFluor™ enables one-step conversion of phenols to aryl fluorides, facilitating fluorination without pre-activation.
Related Content
The Ritter lab currently focuses on fluorination chemistry for late-stage functionalization of complex natural and unnatural products. PhenoFluor™ has been developed as a general reagent for the selective, predictable, direct deoxyfluorination of complex alcohols and phenols.
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