ChemicalBook--->CAS DataBase List--->16799-05-6

16799-05-6

16799-05-6 Structure

16799-05-6 Structure
IdentificationBack Directory
[Name]

3-CHLOROPHENETHYL BROMIDE, 97%
[CAS]

16799-05-6
[Synonyms]

3-CHLOROPHENETHYLBROMIDE,97%
Benzene, 1-(2-bromoethyl)-3-chloro-
[Molecular Formula]

C8H8BrCl
[MDL Number]

MFCD04117465
[MOL File]

16799-05-6.mol
[Molecular Weight]

219.51
Chemical PropertiesBack Directory
[Boiling point ]

85 °C(Press: 0.1 Torr)
[density ]

1.489±0.06 g/cm3(Predicted)
[Fp ]

110 °C
[storage temp. ]

Sealed in dry,Room Temperature
[Appearance]

Colorless to light yellow Liquid
Safety DataBack Directory
[Symbol(GHS) ]

Corrosion (GHS05)Exclamation Mark (GHS07)
GHS05,GHS07
[Signal word ]

Danger
[Hazard statements ]

H302-H318
[Precautionary statements ]

P280-P301+P312+P330-P305+P351+P338+P310
[Hazard Codes ]

Xn,N
[Risk Statements ]

22-41-51/53
[Safety Statements ]

26-36/37-39-61
[RIDADR ]

UN 3082 9/PG 3
[WGK Germany ]

2
[HS Code ]

2903998090
Spectrum DetailBack Directory
[Spectrum Detail]

3-CHLOROPHENETHYL BROMIDE, 97%(16799-05-6)1HNMR
Hazard InformationBack Directory
[Synthesis]

3-CHLOROPHENETHYLALCOHOL

5182-44-5

3-CHLOROPHENETHYL BROMIDE, 97%

16799-05-6

General procedure for the synthesis of 1-(2-bromoethyl)-3-chlorobenzene from 3-chlorobenzene ethanol: Triphenylphosphine (3.90 g, 14.9 mmol) was added to a stirred solution containing 3-chlorobenzene ethanol (2.0 mL, 14.8 mmol), carbon tetrabromide (4.91 g, 14.8 mmol), and anhydrous dichloromethane (100 mL), under nitrogen protection. The reaction mixture was stirred at room temperature for 5 hours. After completion of the reaction, the reaction mixture was washed sequentially with water (100 mL) and brine (100 mL). The organic layer was separated, dried with magnesium sulfate, filtered and concentrated on a rotary evaporator to give the crude product. The crude product was purified by rapid chromatography on silica gel using 100% hexane as eluent to give 2.30 g (71% yield) of 1-(2-bromoethyl)-3-chlorobenzene. Thin layer chromatography (TLC) analysis: Rf value was 0.27 in 100% hexane; 1H NMR (CDCl3) data: δ 7.26-7.11 (m, 3H), 7.09-7.07 (m, 1H), 3.54 (t, 2H), 3.12 (t, 2H).

[References]

[1] Journal of Medicinal Chemistry, 1996, vol. 39, # 20, p. 4017 - 4026
[2] Patent: WO2004/26305, 2004, A1. Location in patent: Page/Page column 67-68
[3] Patent: US2002/19531, 2002, A1
[4] Journal of the Chemical Society, 1964, p. 1548 - 1553
[5] Tetrahedron Asymmetry, 1998, vol. 9, # 15, p. 2725 - 2737
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