| Identification | Back Directory | [Name]
ANTHRACENE, 9-BROMO-10-(1-NAPHTHALENYL)- | [CAS]
400607-04-7 | [Synonyms]
BA1N
9-BroMo-10-(1-naphthyl)anth
racene
10-broMo-9-(phthalen-1-yl)anthracene
9-Bromo-10-(1-naphthalenyl)anthracene
9-Bromo-10-(naphthalen-1-yl)anthracene
10-BroMo-9-(naphthalene-1-yl)Anthracene
10-(naphthalen-1-yl)anthracen-9-broMine
ANTHRACENE, 9-BROMO-10-(1-NAPHTHALENYL)- | [EINECS(EC#)]
1312995-182-4 | [Molecular Formula]
C24H15Br | [MDL Number]
MFCD11046571 | [MOL File]
400607-04-7.mol | [Molecular Weight]
383.286 |
| Chemical Properties | Back Directory | [Melting point ]
177.0 to 181.0 °C | [Boiling point ]
508.0±19.0 °C(Predicted) | [density ]
1.402±0.06 g/cm3(Predicted) | [storage temp. ]
Sealed in dry,Room Temperature | [solubility ]
soluble in Toluene | [form ]
Solid | [color ]
Pale yellow | [InChI]
InChI=1S/C24H15Br/c25-24-21-13-5-3-11-19(21)23(20-12-4-6-14-22(20)24)18-15-7-9-16-8-1-2-10-17(16)18/h1-15H | [InChIKey]
SYACRXBYRNYMLN-UHFFFAOYSA-N | [SMILES]
C1=C2C(C(C3=C4C(C=CC=C4)=CC=C3)=C3C(=C2Br)C=CC=C3)=CC=C1 |
| Questions And Answer | Back Directory | [Uses]
9-Bromo-10-(1-Naphthyl)anthracene is an intermediate in organic synthesis and chemical and pharmaceutical research and development. It is mainly used as an OLED intermediate in laboratory research and development and chemical and pharmaceutical production. | [Application]
9-Bromo-10-(1-Naphthyl)anthracene is a heterocyclic organic compound that can be used as a pharmaceutical intermediate. |
| Hazard Information | Back Directory | [Chemical Properties]
Off-white powder | [Synthesis]
The general procedure for the synthesis of 9-bromo-10-(1-naphthalenyl)anthracene using 9-(naphthalen-1-yl)anthracene as starting material was as follows: 9-(naphthalen-1-yl)anthracene (88 g, 0.29 mol) was dissolved in dimethylformamide (700 mL) in a 2 L four-necked round-bottomed flask. Subsequently, a solution of N-bromosuccinimide (NBS, 70.7 g, 0.4 mol) in dimethylformamide (200 mL) was added slowly and dropwise. The reaction mixture was stirred at room temperature for 2 hours. Upon completion of the reaction, the reaction mixture was poured into water to precipitate 9-bromo-10-(1-naphthyl)anthracene (108 g, 97.5% yield). | [References]
[1] Journal of Materials Chemistry, 2012, vol. 22, # 1, p. 123 - 129
[2] Patent: US2017/12214, 2017, A1. Location in patent: Paragraph 0166; 0167
[3] Chemical Communications, 2016, vol. 52, # 73, p. 10956 - 10959
[4] Patent: KR2016/90242, 2016, A. Location in patent: Paragraph 0266; 0267; 0268; 0269; 0270; 0271
[5] Patent: KR2017/55704, 2017, A. Location in patent: Paragraph 0111; 0118-0123 |
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