TRIETHYL 2-PHOSPHONOBUTYRATE

Bezeichnung:TRIETHYL 2-PHOSPHONOBUTYRATE

CAS-Nr17145-91-4

Englisch Name:TRIETHYL 2-PHOSPHONOBUTYRATE

CBNumberCB6127879

SummenformelC10H21O5P

Molgewicht252.24

MOL-Datei17145-91-4.mol

TRIETHYL 2-PHOSPHONOBUTYRATE physikalisch-chemischer Eigenschaften

Siedepunkt	152-154 °C14 mm Hg(lit.)
Dichte	1.064 g/mL at 25 °C(lit.)
Brechungsindex	n20/D 1.432(lit.)
Flammpunkt	>230 °F
storage temp.	Sealed in dry,Room Temperature
Aggregatzustand	Liquid
Farbe	Clear colorless
Wichte	1.064
Wasserlöslichkeit	Not miscible or difficult to mix with water.
BRN	1789280
InChI	InChI=1S/C10H21O5P/c1-5-9(10(11)13-6-2)16(12,14-7-3)15-8-4/h9H,5-8H2,1-4H3
InChIKey	GYUCVQSNZFRDRL-UHFFFAOYSA-N
SMILES	C(OCC)(=O)C(P(OCC)(OCC)=O)CC

Sicherheit

Kennzeichnung gefährlicher	Xi
R-Sätze:	36/37/38
S-Sätze:	26-36
WGK Germany	3
HS Code	29310099
Speicherklasse	10 - Combustible liquids
Hazard Classifications	Eye Irrit. 2 Skin Irrit. 2 STOT SE 3

Gefahreninformationscode (GHS)

TRIETHYL 2-PHOSPHONOBUTYRATE Chemische Eigenschaften,Einsatz,Produktion Methoden

R-Sätze Betriebsanweisung:
R36/37/38:Reizt die Augen, die Atmungsorgane und die Haut.
S-Sätze Betriebsanweisung:
S26:Bei Berührung mit den Augen sofort gründlich mit Wasser abspülen und Arzt konsultieren.
S36:DE: Bei der Arbeit geeignete Schutzkleidung tragen.
Chemische Eigenschaften
clear colorless liquid
Verwenden
Reactant for preparation of:
- Furospinosulin-1 and analogs as hypoxia-selective antitumor agents
- Aminoquinolines as beta-site amyloid precursor protein cleaving enzyme 1 (BACE1) inhibitors and potential anti-Alzheimer′s drugs
- Phenylpropanoic acid peroxisome proliferator-activated receptor (PPAR) α-selective agonists as nonalcoholic steatohepatitis (NASH)-preventive agents
- PPAR agonists with phenethylphenylphthalimide skeleton derived from thalidomide-related LXR antagonists
- Notch-sparing γ-secretase inhibitors derived from PPAR agonist library
- Plakotenin via Diels-Alder reaction, as a potential anticancer agent, naturally found in Okinawan sponge of the genus Plakortis
- Quinone/naphthoquinone-substituted propenoic acids as inhibitors of cell growth and redox function of apurinic/apyrimidinic endonuclease 1/redox enhancing factor 1 (Ape1/Ref-1)
- α-alkenyl cyclic ethers by asymmetric dehydrative cyclization of ω-hydroxy allyl alcohols catalyzed by Ru complexes of axially chiral naphthylpyridinecarboxylates
- Branched phosphonoethoxyethyl purines as new acyclic nucleoside phosphonates which inhibit Plasmodium falciparum (malarial parasite) hypoxanthine-guanine-xanthine phosphoribosyltransferase (HGXPRT)
- Phenylpropanoic acid-type peroxisome proliferator-activated receptor pan agonists as candidate drugs for treatment of altered metabolic homeostasis
Verwenden
Reactant used for preparation of furospinosulin-1 and analogs as hypoxia-selective antitumor agents, Aminoquinolines as beta-site amyloid precursor protein cleaving enzyme 1 (BACE1) inhibitors and potential anti-Alzheimers drugs, phenylpropanoic acid peroxisome proliferator-activated receptor (PPAR) α-selective agonists as nonalcoholic steatohepatitis (NASH)-preventive agents, PPAR agonists with phenethylphenylphthalimide skeleton derived from thalidomide-related LXR antagonists, notch-sparing γ-secretase inhibitors derived from PPAR agonist library and plakotenin via Diels-Alder reaction, as a potential anticancer agent, naturally found in Okinawan sponge of the genus Plakortis.
reaction suitability
reaction type: C-C Bond Formation

TRIETHYL 2-PHOSPHONOBUTYRATE Upstream-Materialien And Downstream Produkte

TRIETHYL 2-PHOSPHONOBUTYRATE Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

17145-91-4, TRIETHYL 2-PHOSPHONOBUTYRATE Verwandte Suche:

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