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371963

Hexafluoropropene, trimer

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About This Item

Linear Formula:
[CF3C(F)=CF2]3
CAS Number:
6792-31-0
Molecular Weight:
450.07
NACRES:
NA.22
PubChem Substance ID:
24863138
UNSPSC Code:
12352100
MDL number:
MFCD00043821

Key Documents

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InChI

1S/3C3F6/c3*4-1(2(5)6)3(7,8)9

SMILES string

FC(F)=C(F)C(F)(F)F.FC(F)=C(F)C(F)(F)F.FC(F)=C(F)C(F)(F)F

InChI key

VJRSWIKVCUMTFK-UHFFFAOYSA-N

form

liquid

bp

110-115 °C (lit.)

density

1.83 g/mL at 25 °C (lit.)

functional group

fluoro

Quality Level

100

Related Categories

Application

Hexafluoropropene, trimer may be used in the preparation of photochromic spiroindolinonaphthoxazine derivative. It may be used in the preparation of 2-trifluoromethyl-3-heptadifluoroisopropyl-2-perfluoropentene-4-(N′,N′-dimethylamino propyl) imino(I).

General description

Spectra of three isomeric trimers of hexafluoropropene have been investigated. It reacts with primary amines, via indirect substitution of fluorine atoms, to form the corresponding enamines and enimines.

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

75.2 °F - closed cup

flash_point_c

24 °C - closed cup

ppe

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

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Certificates of Analysis (COA)

Lot/Batch Number
STBK9975
STBK5530
STBK5036
STBK1970
STBF2489V

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C C Geilen et al.
FEBS letters, 309(3), 381-384 (1992-09-14)
In this study, we report that the potent and selective inhibitor of cyclic AMP-dependent protein kinase, N-[2-bromocinnamyl(amino)ethyl]-5-isoquinolinesulfonamide (H-89) interferes with the incorporation of choline into phosphatidylcholine in HeLa cells. Treatment of cells with 10 microM H-89 for 1 h decreases
W L Combest et al.
Journal of neurochemistry, 51(5), 1581-1591 (1988-11-01)
The effects of the naturally occurring polyamines spermine and spermidine on phosphorylation promoted by cyclic AMP (cAMP)-dependent protein kinase (PK) (cAMP-PK; EC 2.7.1.37) were studied using the brain of the tobacco hornworm, Manduca sexta. Four particulate-associated peptides (280, 34, 21
H Kawasaki et al.
Science (New York, N.Y.), 282(5397), 2275-2279 (1998-12-18)
cAMP (3',5' cyclic adenosine monophosphate) is a second messenger that in eukaryotic cells induces physiological responses ranging from growth, differentiation, and gene expression to secretion and neurotransmission. Most of these effects have been attributed to the binding of cAMP to
Synthesis of Fluoro-tertiary and Quaternary Ammonium Cationic Surfactants [J].
Jingfeng LZ, et al.
Dyestuffs and Coloration / Ran Liao Yu Ran Shai, 1, 009-009 (2006)
Jost Leemhuis et al.
The Journal of pharmacology and experimental therapeutics, 300(3), 1000-1007 (2002-02-28)
The small GTPase RhoA can retract cell extensions by acting on two Rho kinases (ROCKs). Activated protein kinase A (PKA) inhibits RhoA and induces extensions. The isoquinoline H89 inhibits PKA and thus should prevent the inactivation of RhoA. In kinase
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