ChemicalBook--->CAS DataBase List--->3383-72-0

3383-72-0

3383-72-0 Structure

3383-72-0 Structure
IdentificationMore
[Name]

1-(2-Chloroethoxy)-4-nitrobenzene
[CAS]

3383-72-0
[Synonyms]

1-(2-CHLOROETHOXY)-4-NITROBENZENE
2-(4-NITROPHENOXY)ETHYL CHLORIDE
BETA-CHLORO-4-NITROPHENETHOLE
2-CHLOROETHYL-4-NITROPHENYL ETHER
β-chloro-4-nitrophenethole
1-(2-CHLOROETHOXY)4-NITROBENZENE, 98+%
[EINECS(EC#)]

425-790-8
[Molecular Formula]

C8H8ClNO3
[MDL Number]

MFCD00674505
[Molecular Weight]

201.61
[MOL File]

3383-72-0.mol
Chemical PropertiesBack Directory
[Melting point ]

67-68 °C
[Boiling point ]

204-206 °C(Press: 25 Torr)
[density ]

1.316±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

powder to crystal
[color ]

White to Light yellow
[InChI]

InChI=1S/C8H8ClNO3/c9-5-6-13-8-3-1-7(2-4-8)10(11)12/h1-4H,5-6H2
[InChIKey]

OBCFOPGCTNULTG-UHFFFAOYSA-N
[SMILES]

C1(OCCCl)=CC=C([N+]([O-])=O)C=C1
[CAS DataBase Reference]

3383-72-0(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
[WGK Germany ]

3
[F ]

9-21
[Hazard Note ]

Irritant
[REACH Registrations]

Inactive
[HazardClass ]

IRRITANT
[HS Code ]

2909309090
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

3383-72-0(sigmaaldrich)
Hazard InformationBack Directory
[Synthesis]

4-Nitrophenol

100-02-7

1-Bromo-2-chloroethane

107-04-0

1-(2-Chloroethoxy)-4-nitrobenzene

3383-72-0

1-(2-Chloroethoxy)-4-nitrobenzene was synthesized as follows: cesium carbonate (28.7 mmol) was added to a solution of 4-nitrophenol (28.7 mmol) in anhydrous ethanol (15 mL), followed by 1-bromo-2-chloroethane (86.2 mmol). The reaction mixture was heated to reflux at 80 °C for 8 hours. Upon completion of the reaction, the mixture was cooled, the reaction was quenched with water and extracted with ethyl acetate (EtOAc). The organic layers were combined, washed sequentially with water and brine, dried over anhydrous sodium sulfate (Na2SO4) and concentrated under reduced pressure to give an orange residue. Grinding of the residue with ethanol (EtOH) gave 1-(2-chloroethoxy)-4-nitrobenzene in 66% yield. Mass spectrum (MS) (m/z): (M+1)+ 202.2.

[References]

[1] Patent: WO2007/38669, 2007, A2. Location in patent: Page/Page column 170
[2] Journal of Medicinal Chemistry, 2006, vol. 49, # 16, p. 4981 - 4991
[3] Patent: WO2005/68452, 2005, A1. Location in patent: Page/Page column 41
[4] Journal of Medicinal Chemistry, 2008, vol. 51, # 6, p. 1637 - 1648
[5] Patent: WO2004/5282, 2004, A1. Location in patent: Page 39
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