(S)-(+)-1,2,3,4-Tetrahydro-1-naphthol
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- CAS-Nr.
- 53732-47-1
- Englisch Name:
- (S)-(+)-1,2,3,4-Tetrahydro-1-naphthol
- Synonyma:
- J330.337C;(S)-1-tetralol;1-Tetralol, (S)-;(s)-(+)-α-tetralol;(S)-1-Hydroxytetralin;(S)-(+)-ALPHA-TETRALOL;1Tetralol, (S),1 Tetralol, (S);(S)-(+)-1,2,3,4-tetrahydro-1-naphtol;(S)-(+)-1,2,3,4-TETRAHYDRO-1-NAPHTHOL;(S)-1,2,3,4-Tetrahydronaphthalen-1-ol
- CBNumber:
- CB8427865
- Summenformel:
- C10H12O
- Molgewicht:
- 148.2
- MOL-Datei:
- 53732-47-1.mol
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(S)-(+)-1,2,3,4-Tetrahydro-1-naphthol Eigenschaften
- Schmelzpunkt:
- 37-39 °C
- Siedepunkt:
- 92 °C / 1.8mmHg
- Dichte
- 1.09 g/mL at 25 °C(lit.)
- Brechungsindex
- 33 ° (C=2.5, CHCl3)
- Flammpunkt:
- 113 °C
- Löslichkeit
- almost transparency in Methanol
- Aggregatzustand
- powder to crystal
- pka
- 14.33±0.20(Predicted)
- Farbe
- White to Almost white
- Optische Aktivität
- [α]20/D +33±1°, c = 2.5% in chloroform
- BRN
- 2208779
- CAS Datenbank
- 53732-47-1(CAS DataBase Reference)
(S)-(+)-1,2,3,4-Tetrahydro-1-naphthol 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.
Verwenden
(S)?-?(+)?-?1,?2,?3,?4-?Tetrahydro-?1-?naphthol is a building block used in pharmaceutical chemistry such as in the synthesis of a potent and orally bioavailable GPR40 agonist acting as a novel insulin secretagogues with low risk of hypoglycemia
Allgemeine Beschreibung
Chiral building block.
(S)-(+)-1,2,3,4-Tetrahydro-1-naphthol Upstream-Materialien And Downstream Produkte
Upstream-Materialien
Downstream Produkte
(S)-(+)-1,2,3,4-Tetrahydro-1-naphthol Anbieter Lieferant Produzent Hersteller Vertrieb Händler.
Global( 84)Lieferanten
53732-47-1()Verwandte Suche:
Phenmedipham
Terbutaline
1,1'-Binaphthyl-2,2'-diol
4-(α-(4-Hydroxy-1-naphthyl)benzyliden)naphthalin-1(4H)-on
4-Hydroxy-α-(4-hydroxynaphthyl)-α-phenylnaphthalin-1-methanol
2-Naphthol
1-Naphthol
Oxytetracyclinhydrochlorid
Demeclocyclinhydrochlorid
1-Naphthacencarbonsure, 2-Ethyl-1,2,3,4,6,11-hexahydro-2,5,7-trihydroxy-6,11-dioxo-4-[[2,3,6-trideoxy-4-O-[2,6-dideoxy-4-O-[(2R-trans)-tetrahydro-6-methyl-5-oxo-2H-pyran-2-yl]-α-L-lyxo-hexopyranosyl]-3-(dimethylamino)-α-L-lyxo-hexopyranosyl]oxy]-, Methylester, Hydrochlorid, [1R-(1α,2β,4β)]-
2-Naphthacencarbonsure-amid, 7-Chlor-4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,6,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-, Monohydrochlorid, [4S-(4α,4aα,5aα,6β,12aα)]-
Tetracyclin
Doxorubicin
Tetracyclinhydrochlorid
Metaphosphorsure, Natriumsalz, Verbindung mit [4S-(4α,4aα,5aα,6β,12aα)]-4-(Dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,6,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-2-naphthacencarboxamid
2-Naphthacencarboxamid, 4-(Dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,5,6,10,12,12a-hexahydroxy-6-methyl-1,11-dioxo-, Calciumsalz, [4S-(4α,4aα,5α,5aα,6β,12aα)]-
1,2,3,4-Tetrahydro-2-naphthalinol
alpha-Tetralol
- (S)-(+)-ALPHA-TETRALOL
- (S)-(+)-1,2,3,4-TETRAHYDRO-1-NAPHTHOL
- (S)-(+)-1,2,3,4-TETRAHYDRO-1-NAPHTHOL, 9 9% (99% EE/HPLC)
- (S)-(+)-1,2,3,4-tetrahydro-1-naphtol
- (s)-(+)-α-tetralol
- (S)-1,2,3,4-Tetrahydronaphthalen-1-ol
- (S)-(+)-1,2,3,4-Tetrahydro-1-naphthol 99%
- (S)-(+)-1,2,3,4-Tetrahydro-1-naphthol
- (S)-1,2,3,4-Tetrahydro-1-naphthol,99%e.e.
- 1-Naphthalenol,1,2,3,4-tetrahydro-, (1S)-
- (S)-1-tetralol
- (1S)-1,2,3,4-tetrahydronaphthalen-1-ol
- (S)-1-Hydroxytetralin
- 1-Tetralol, (S)-
- J330.337C
- 1Tetralol, (S),1 Tetralol, (S)
- 53732-47-1
- Organic Building Blocks
- Alcohols
- Chiral Building Blocks
- Asymmetric Synthesis
- Chiral Building Blocks
- Simple Alcohols (Chiral)
- Synthetic Organic Chemistry
- Chiral
