1-ACENAPHTHENOL

1-ACENAPHTHENOL Basic information
Product Name:1-ACENAPHTHENOL
Synonyms:1-Acenaphthenol (Acenaphthene-1-hydroxy);1-Acenaphthylenol, 1,2-dihydro- (9CI);A406_ALDRICH;Acenaphthene-1-ol;EINECS 228-618-8;NSC 22834;NSC22834;28807-94-5
CAS:6306-07-6
MF:C12H10O
MW:170.21
EINECS:228-618-8
Product Categories:Aromatic Phenols
Mol File:6306-07-6.mol
1-ACENAPHTHENOL Structure
1-ACENAPHTHENOL Chemical Properties
Melting point 145-148 °C (lit.)
Boiling point 369℃
density 1.290
Fp 129℃
storage temp. -20°C Freezer
solubility Chloroform (Slightly, Sonicated), Methanol (Slightly)
pka13.68±0.20(Predicted)
form Solid
color Yellow to Dark Yellow
BRN 2048222
Stability:Stable. Combustible. Incompatible with strong oxidizing agents.
CAS DataBase Reference6306-07-6(CAS DataBase Reference)
Safety Information
WGK Germany 3
HS Code 2906.29.6000
HazardClass IRRITANT
MSDS Information
ProviderLanguage
SigmaAldrich English
ALFA English
1-ACENAPHTHENOL Usage And Synthesis
Description1-Acenaphthenol is a white to cream solid in appearance. It is almost insoluble in water. 1-Acenaphthenol is a stable and combustible chemical substance. It is incompatible with strong oxidising agents. It is used in the syntheses of organic compounds. Exposures to 1-acenaphthenol cause irritant effects. It is harmful by ingestion, inhalation, as well as through skin absorption. There are no complete data on the toxicology of 1-acenaphthenol.
Chemical Properties1-Acenaphthenol is a white to cream solid in appearance. It is almost insoluble in water. 1-Acenaphthenol is a stable and combustible chemical substance. It is incompatible with strong oxidizing agents. It is used in the syntheses of organic compounds.
Uses1-Acenaphthenol is a product of the microbial metabolism and photolysis of acenaphthene, of acenaphthene, a polycyclic hydrocarbon that has potential to act as polyploidizing agents in plants. 1-Acenaphthenol is also a known substrate of dihydrodiol dehydrogenases.
Health HazardExposures to 1-acenaphthenol cause irritant effects. It is harmful by ingestion, inhalation, or skin absorption. There are no complete data on the toxicology of 1-acenaphthenol.
Purification MethodsIf highly coloured (yellow), dissolve it in boiling *benzene (14g in 200mL), add charcoal (0.5g), filter it through a heated funnel, concentrate to 100mL and cool to give almost colourless needles. *Benzene vapour is TOXIC; use an efficient fume cupboard. The acetate has b 166-168o/5mm (bath temperature 180-185o). [Cason Org Synth Coll Vol III 3 1955.] It can also be recrystallised from *C6H6 or EtOH [Fieser & Cason J Am Chem Soc 62 432 1940]. It forms a brick-red crystalline complex with 2,4,5,7-tetranitrofluoren-9-one which is recrystallised from AcOH and is dried in a vacuum over KOH and P2O5 at room temperature, m 170-172o [Newman & Lutz J Am Chem Soc 78 2469 1956]. [Beilstein 6 IV 4623.]
1-hydroxy-3-methylcholanthrene 1-ACETOXYACENAPHTHENE 1-Acenaphthenol, 5-nitro- 1-ACENAPHTHENOL 3-Acetoxy-3,4-dihydrocyclopenta(cd)pyrene 2-hydroxy-3-methylcholanthrene 1,9,10-Trihydroxy-9,10-dihydro-3-methylcholanthrene 1-Acetoxy-3-methylcholanthrene cyclopenta(cd)pyrene 3,4-oxide 4-Acetoxy-3,4-dihydrocyclopenta(cd)pyrene Acenaphthene SPECS AE-562/12222219 2-Acetoxy-3-methylcholanthrene 3-Hydroxy-3,4-dihydrocyclopenta(cd)pyrene 5-ACENAPHTHENOL 1,2-DIHYDROXY-1,2-DIMETHYL-ACENAPHTHENE

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