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Key Documents

Altri documenti

371963

Sigma-Aldrich

Hexafluoropropene, trimer

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About This Item

Formula condensata:
[CF3C(F)=CF2]3
Numero CAS:
6792-31-0
Peso molecolare:
450.07
Numero MDL:
MFCD00043821
Codice UNSPSC:
12352100
ID PubChem:
24863138
NACRES:
NA.22

Forma fisica

liquid

Livello qualitativo

100

P. eboll.

110-115 °C (lit.)

Densità

1.83 g/mL at 25 °C (lit.)

Stringa SMILE

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

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

Categorie correlate

Descrizione generale

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.

Applicazioni

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).

Pittogrammi

FlameExclamation mark
GHS02,GHS07

Avvertenze

Warning

Classi di pericolo

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

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

3 - Flammable liquids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

75.2 °F - closed cup

Punto d’infiammabilità (°C)

24 °C - closed cup

Dispositivi di protezione individuale

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

Certificati d'analisi (COA)

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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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