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ChemicalBook--->CAS DataBase List--->5856-33-7

5856-33-7

5856-33-7 Structure

5856-33-7 Structure
IdentificationBack Directory
[Name]

BETA-NAPHTHYL BUTYRATE
[CAS]

5856-33-7
[Synonyms]

BETA-NAP-BUTYRATE
2-NAPHTHYL BUTYRATE
RARECHEM AH BS 0061
B-naphthyl butyrate
BETA-NAPHTHYL BUTYRATE
BETA-NAPHTHYL-N-BUTYRATE
Naphthalen-2-yl butyrate
NAPHTHALEN-2-YL BUTANOATE
Butyric acid-b-naphthyl ester
BUTANOIC ACID 2-NAPHTHYL ESTER
BUTYRIC ACID-BETA-NAPHTHYL ESTER
Butanoic acid, 2-naphthalenyl ester
[Molecular Formula]

C14H14O2
[MDL Number]

MFCD00046464
[MOL File]

5856-33-7.mol
[Molecular Weight]

214.26
Chemical PropertiesBack Directory
[Boiling point ]

164-165 °C
[density ]

1.12 g/mL at 25 °C(lit.)
[storage temp. ]

Sealed in dry,Store in freezer, under -20°C
Safety DataBack Directory
[Symbol(GHS) ]


GHS07,GHS09
[Signal word ]

Warning
[Hazard statements ]

H302+H332-H400
[Precautionary statements ]

P273
[Hazard Codes ]

Xn,N
[Risk Statements ]

20/22-50
[Safety Statements ]

61
[RIDADR ]

UN 3082 9 / PGIII
[WGK Germany ]

3
Hazard InformationBack Directory
[Uses]

2-Naphthyl Butyrate (cas# 5856-33-7) is a compound useful in organic synthesis.
[Definition]

ChEBI: 2-naphthyl butyrate is a butyrate ester obtained by formal condensation of the carboxy group of butyric acid with the hydroxy group of 2-naphthol. It has a role as a chromogenic compound. It is a member of naphthalenes, a butyrate ester and an aromatic ester. It is functionally related to a 2-naphthol.
[Synthesis]

Vinyl butyrate

123-20-6

2-Naphthol

135-19-3

BETA-NAPHTHYL BUTYRATE

5856-33-7

The general procedure for the synthesis of 2-naphthyl butyrate from 2-naphthol and vinyl n-butyrate was as follows: a mixture of 2-naphthol (0.50 mmol), Na2CO3 (10.6 mg, 0.10 mmol, 20 mol%), and vinyl n-butyrate (2.0 mmol, 4.0 eq.) in acetonitrile (3 mL) was added to a 25 mL Schlenk flask. The reaction mixture was stirred at 120 °C until the reaction was complete. Subsequently, the solvent was removed by distillation under reduced pressure and the residue was purified by column chromatography (eluent: petroleum ether/ethyl acetate from 20:1 to 10:1) to afford the target product 2-naphthyl butyrate.

[References]

[1] Synlett, 2018, vol. 29, # 17, p. 2321 - 2325
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