ChemicalBook--->CAS DataBase List--->75476-78-7

75476-78-7

75476-78-7 Structure

75476-78-7 Structure
IdentificationBack Directory
[Name]

1H-INDENE, 5-BROMO-
[CAS]

75476-78-7
[Synonyms]

SKL641
5-BROMO-1H-INDENE
1H-INDENE, 5-BROMO-
5-Bromo-1H-indene 95+%
[Molecular Formula]

C9H7Br
[MDL Number]

MFCD03659729
[MOL File]

75476-78-7.mol
[Molecular Weight]

195.06
Chemical PropertiesBack Directory
[Melting point ]

36 °C
[Boiling point ]

120 °C(Press: 16 Torr)
[density ]

1.523±0.06 g/cm3(Predicted)
[storage temp. ]

Store at room temperature
[Appearance]

White to off-white Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

P280-P305+P351+P338
[Hazard Codes ]

Xi
[HS Code ]

2903998090
Spectrum DetailBack Directory
[Spectrum Detail]

1H-INDENE, 5-BROMO-(75476-78-7)1HNMR
Hazard InformationBack Directory
[Synthesis]

6-BROMO-2,3-DIHYDRO-1H-INDEN-1-OL

75476-86-7

1H-INDENE, 5-BROMO-

75476-78-7

General procedure for the synthesis of 5-bromo-1H-indene from 6-bromo-2,3-dihydro-1H-inden-1-ol: 170 g of 6-bromo-2,3-dihydro-1H-inden-1-ol, 1.2 L of hydroxybenzenesulphonic acid, p-toluenesulphonic acid, and 8 g of catalyst were added to a reaction flask for 3 hours. After completion of the reaction, benzene was removed by distillation. The crude product was purified by fast chromatography to give 148 g of 5-bromo-1H-indene (in the form of coral oil) in 95% yield.

[References]

[1] Journal of Organic Chemistry, 1984, vol. 49, # 22, p. 4226 - 4237
[2] Patent: JP2016/29040, 2016, A. Location in patent: Paragraph 0059
[3] Organic and Biomolecular Chemistry, 2003, vol. 1, # 8, p. 1298 - 1307
[4] Journal of Organic Chemistry, 1980, vol. 45, # 26, p. 5312 - 5315
[5] Bioorganic and Medicinal Chemistry Letters, 1999, vol. 9, # 12, p. 1657 - 1662
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