4-Acetoxyindole Struktur

4-Acetoxyindole

Bezeichnung:4-Acetoxyindole

CAS-Nr5585-96-6

Englisch Name:4-Acetoxyindole

CBNumberCB4477655

SummenformelC10H9NO2

Molgewicht175.18

MOL-Datei5585-96-6.mol

4-Acetoxyindole physikalisch-chemischer Eigenschaften

Schmelzpunkt	100-102°C
Siedepunkt	339.1±15.0 °C(Predicted)
Dichte	1?+-.0.06 g/cm3(Predicted)
storage temp.	2-8°C
Löslichkeit	Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly)
Aggregatzustand	Solid
pka	16.38±0.30(Predicted)
Farbe	Off-White to Beige
InChI	InChI=1S/C10H9NO2/c1-7(12)13-10-4-2-3-9-8(10)5-6-11-9/h2-6,11H,1H3
InChIKey	ZXDMUHFTJWEDEF-UHFFFAOYSA-N
SMILES	N1C2=C(C(OC(=O)C)=CC=C2)C=C1
CAS Datenbank	5585-96-6(CAS DataBase Reference)

Sicherheit

Kennzeichnung gefährlicher	Xi
WGK Germany	3
Hazard Note	Irritant
HS Code	2933998090

Gefahreninformationscode (GHS)

4-Acetoxyindole Chemische Eigenschaften,Einsatz,Produktion Methoden

Beschreibung
4-acetoxylindole is also known as 4-Indolyl acetate. It can be used as standards of the reverse phase HPLC during separation of small molecules. It can also be used as reactant during the preparation of inhibitors of HIV-attachment, prostanoid EP3 antagonist, indolyl-nitroalkanes and psilocybin.
Verwenden
Reactant for preparation of:• ;Inhibitors of HIV-1 attachment1• ;Prostanoid EP3 receptor antagonist, as a novel antiplatelet agent2• ;Indolyl-nitroalkanes via N-bromosuccinimide catalyzed synthesis3• ;Psilocybin as a medicinal agent4
Verwenden
4-Acetoxyindole is a useful intermediate for organic synthesis of Psilocine and Psilocine analogs.
Verwenden
Reactant for preparation of:
- Inhibitors of HIV-1 attachment
- Prostanoid EP3 receptor antagonist, as a novel antiplatelet agent
- Indolyl-nitroalkanes via N-bromosuccinimide catalyzed synthesis
- Psilocybin as a medicinal agent
Allgemeine Beschreibung
4-Acetoxyindole is a chromophore that belongs to the pyrrole family of compounds. It has been shown to react with an ionic liquid under acidic conditions to form a protonated intermediate, which can be deprotonated by a nucleophile. This reaction yields an acetate anion and a fluorescing product. 4-Acetoxyindole also reacts with deuterium gas, yielding an acetate, a deuterium atom, and fluorescing product. The reaction is reversible and the yield of the product depends on the concentration of the reactants. 4-Acetoxyindole has strong carbonyl groups that make it reactive towards other functional groups. These reactions are useful for synthesizing heterocycles such as indoles and isoquinolines.
Einzelnachweise
http://www.sigmaaldrich.com/catalog/product/aldrich/259047?lang=en&region=US
https://pubchem.ncbi.nlm.nih.gov/compound/4-Acetoxyindole

4-Acetoxyindole Upstream-Materialien And Downstream Produkte

4-Acetoxyindole Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

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