1-Tetralone

1-Tetralone Basic information
Product Name:1-Tetralone
Synonyms:KETOTETRAHYDRONAPHTHALENE;1,2,3,4-TETRAHYDRO-1-NAPHTHALENONE;1-TETRALONE;3,4-DIHYDRO-1-(2H)NAPHTHALENEONE;1,2,3,4-Tetrahydro-1-oxonaphthalene;1-Tetralone,97%;1(2H)-Naphthalenone, 3,4-dihydro-;à-Tetralone
CAS:529-34-0
MF:C10H10O
MW:146.19
EINECS:208-460-6
Product Categories:Bioactive Small Molecules;Building Blocks;C10;Carbonyl Compounds;Cell Biology;Chemical Synthesis;Ketones;Organic Building Blocks;T;PHARMACEUTICAL INTERMEDIATES;Cardiovascular & Blood System Agents;pharmaceutical;bc0001;529-34-0
Mol File:529-34-0.mol
1-Tetralone Structure
1-Tetralone Chemical Properties
Melting point 2-7 °C(lit.)
Boiling point 113-116 °C6 mm Hg(lit.)
density 1.099 g/mL at 25 °C(lit.)
refractive index n20/D 1.568(lit.)
Fp >230 °F
storage temp. 2-8°C
solubility Chloroform, Ethyl Acetate (Slightly)
form Liquid
color brown
Water Solubility insoluble
BRN 607374
InChIKeyXHLHPRDBBAGVEG-UHFFFAOYSA-N
CAS DataBase Reference529-34-0(CAS DataBase Reference)
NIST Chemistry Reference1(2H)-Naphthalenone, 3,4-dihydro-(529-34-0)
EPA Substance Registry System1,2,3,4-Tetrahydronaphthalen-1-one (529-34-0)
Safety Information
Hazard Codes Xn
Risk Statements 22-20/22-20/21/22
Safety Statements 23-24/25-36
WGK Germany 3
RTECS QK4375000
TSCA Yes
HS Code 29143900
Hazardous Substances Data529-34-0(Hazardous Substances Data)
ToxicityLD50 orally in Rabbit: 810 mg/kg LD50 dermal Rabbit > 2200 mg/kg
MSDS Information
ProviderLanguage
1-Tetralone English
SigmaAldrich English
ACROS English
ALFA English
1-Tetralone Usage And Synthesis
Chemical PropertiesClear amber to brown oily liquid
Uses1-Tetralone is a reagent used in the synthesis of amino-pyrazolopyridines with anti-NF-κB and pro-apoptotic potential.
Synthesis Reference(s)Tetrahedron Letters, 32, p. 4291, 1991 DOI: 10.1016/S0040-4039(00)92151-8
Purification MethodsCheck the IR first. Purify α-tetralone by dissolving 20mL in Et2O (200mL), washing with H2O (100mL), 5% aqueous NaOH (100mL), H2O (100mL), 3% aqueous AcOH (100mL), 5% NaHCO3 (100mL) then H2O (100mL) and dry the ethereal layer over MgSO4. Filter, evaporate and fractionate the residue through a 6in Vigreux column (p 11) under reduced pressure to give a colourless oil (~17g) with b 90-91o/0.50.7mm. [Snyder & Werber Org Synth Coll Vol III 798 1955.] It has also been fractionated through a 0.5metre packed column with a heated jacket under reflux using a partial take-off head. It has max 247.5 and 290nm (hexane). The phenylhydrazone has m 83o. The 2,4,6-trinitrophenylhydrazone has m 247.5-248o (from EtOH). [Olson & Bader Org Synth Coll Vol IV 898 1963, Beilstein 7 H 370, 7 III 1416, 7 IV 1015.]
5-Methoxy-1-tetralone,97% Tetrahydro 1-ACETOXY-8-HYDROXY-1,4,4A,9A-TETRAHYDROANTHRAQUINONE BUTTPARK 104\40-45 4-PHENYL-3,4-DIHYDRO-2H-NAPHTHALEN-1-ONE BUTTPARK 110\40-65 9,10-DIHYDROBENZO[A]PYREN-7(8H)-ONE 4-(3,4-Dichloropheny1)-1-Tetralone(ForSertralineHcl) 1,2,3,6,7,8,11,12-OCTAHYDROBENZO[E]PYREN-9(10H)-ONE 2,3-DIHYDRO-9,10-DIHYDROXY-1,4-ANTHRACENEDIONE 6-((4-amidinobenzoyl)amino)tetralone-2-acetic acid 1-METHYL-2-TETRALONE 1,4,4A,9A-TETRAHYDROANTHRAQUINONE, TECH. , 90 2,3-DIHYDRO-1H-PHENANTHREN-4-ONE 5,6,8,9-TETRAHYDROBENZ[A]ANTHRACEN-11(10H)-ONE 5-Hydroxy-2-tetralone 6-hydroxyl-2-tetralone Bromo-3,3,6,8-tetramethyl-1-tetralone

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