“Hexafluoropropylene”的意思、由来-开放百科全书

词条

Hexafluoropropylene

释义

References

{{Chembox
| verifiedrevid = 420876606
| Name = Hexafluoropropylene
| ImageFileL1 = Hexafluoropropylene.svg
| ImageSizeL1 = 125
| ImageAltL1 = Structural formula of hexafluoropropylene
| ImageFileR1 = Hexafluoropropylene 3D.png
| ImageSizeR1 = 125
| ImageAltR1 = Ball-and-stick model of the hexafluoropropylene molecule
| IUPACName = Hexafluoropropene
| OtherNames = Perfluoropropene,
Perfluoropropylene,
freon R 1216,
halocarbon R 1216,
fluorocarbon 1216
|Section1={{Chembox Identifiers
| SMILES = F/C(F)=C(/F)C(F)(F)F
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID = 8001
| InChI = 1/C3F6/c4-1(2(5)6)3(7,8)9
| InChIKey = HCDGVLDPFQMKDK-UHFFFAOYAV
| StdInChI_Ref = {{stdinchicite|correct|chemspider}}
| StdInChI = 1S/C3F6/c4-1(2(5)6)3(7,8)9
| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
| StdInChIKey = HCDGVLDPFQMKDK-UHFFFAOYSA-N
| CASNo_Ref = {{cascite|correct|CAS}}
| CASNo = 116-15-4
| UNII_Ref = {{fdacite|correct|FDA}}
| UNII = TRW23XOS20
| RTECS = UD0350000
| PubChem = 8302
| UNNumber = 1858
| EINECS = 204-127-4
|Section2={{Chembox Properties
| C=3 | F=6
| Appearance = Colorless, odorless gas
| Density = 1.332 g/ml, liquid at 20 °C
| Solubility = Insoluble
| MeltingPtC = -153
| BoilingPtC = -28
|Section7={{Chembox Hazards
| ExternalSDS =
| MainHazards = Suffocation
| NFPA-H = 1
| NFPA-F = 0
| NFPA-R = 1
| FlashPt = Non flammable gas
| GHSPictograms = {{GHS04}}{{GHS07}}{{GHS08}}
| GHSSignalWord = Warning
| HPhrases = {{H-phrases|280|332|335|351|371|373}}
| PPhrases = {{P-phrases|201|202|260|261|264|270|271|281|304+312|304+340|308+313|309+311|312|314|403+233|405|410+403|501}}
|Section8={{Chembox Related
| OtherFunction_label = alkenes;
organofluorides
| OtherFunction = propylene;
Hexafluoroacetone, Hexafluoro-2-propanol
}}Hexafluoropropylene is a compound with the formula C₃F₆. It is a fluorocarbon alkene in which all of the hydrogen atoms in propylene are replaced by fluorine atoms. It is used as a chemical intermediate.^[1]

References

1. ^{{cite journal | last=Lehmler |first=HJ| title=Synthesis of environmentally relevant fluorinated surfactants—a review| journal=Chemosphere |volume=58 |issue=11 |pages=1471–96 |date=March 2005| doi=10.1016/j.chemosphere.2004.11.078 |pmid=15694468 }}

1 : Organofluorides

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