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2-(2'-BROMOPHENOXY)PROPANE

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Products Intro: Product Name:2-(2'-BROMOPHENOXY)PROPANE
CAS:701-07-5
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Products Intro: Product Name:2-(2'-Bromophenoxy)propane
CAS:701-07-5
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Products Intro: Product Name:1-Bromo-2-isopropoxybenzene
CAS:701-07-5
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Products Intro: Product Name:1-Bromo-2-Isopropoxybenzene
CAS:701-07-5
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Products Intro: Product Name:2-(2'-Bromophenoxy)propane
CAS:701-07-5
Purity:99% Package:1G;1KG;100KG Remarks:AS03456

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  • $101.00 / 1KG
  • 2025-09-25
  • CAS:701-07-5
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  • Purity: 99%
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2-(2'-BROMOPHENOXY)PROPANE Basic information
Product Name:2-(2'-BROMOPHENOXY)PROPANE
Synonyms:1-bromo-2-propan-2-yloxybenzene;1-Bromo-2-isopropoxybenzen;2-BROMOISOPROPOXYBENZENE;2-(2'-BROMOPHENOXY)PROPANE;O-BROMOISOPROPOXYBENZENE;1-Bromo-2-isopropoxybenzene;1-Bromo-2-isopropoxybenzene >;Benzene, 1-bromo-2-(1-methylethoxy)-
CAS:701-07-5
MF:C9H11BrO
MW:215.09
EINECS:
Product Categories:Anisoles, Alkyloxy Compounds & Phenylacetates;Bromine Compounds
Mol File:701-07-5.mol
2-(2'-BROMOPHENOXY)PROPANE Structure
2-(2'-BROMOPHENOXY)PROPANE Chemical Properties
Boiling point 73 °C / 2mmHg
density 1.34
refractive index 1.5360-1.5400
storage temp. Sealed in dry,Room Temperature
form clear liquid
color Colorless to Light yellow
Water Solubility Slightly soluble in water.
CAS DataBase Reference701-07-5(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36/37/39
HS Code 2909309090
MSDS Information
2-(2'-BROMOPHENOXY)PROPANE Usage And Synthesis
Chemical PropertiesColorless liquid
Uses1-Bromo-2-isopropoxybenzene is used as an intermediate in organic syntheses.
Synthesis
2-Bromophenol

95-56-7

2-Bromopropane

75-26-3

2-(2'-BROMOPHENOXY)PROPANE

701-07-5

General procedure for the synthesis of 1-bromo-2-isopropoxybenzene from 2-bromophenol and 2-bromopropane: A mixture of 2-bromophenol (1.156 mmol), anhydrous K2CO3 (1.20 eq., 192 mg), sodium iodide (4 mg), and anhydrous ethanol (3 mL) was magnetically stirred at room temperature under argon protection. 2-Bromopropane (1.20 eq.) was added slowly and the mixture was then refluxed for 5 hours. After the reaction was complete, it was cooled to room temperature and the solvent was removed under reduced pressure. Ethyl acetate (50 mL) was added to dissolve the residue and the organic phase was washed sequentially with 1M NaOH and brine (15 mL each). The organic phase was dried with anhydrous Na2SO4 and the solvent was evaporated under reduced pressure to obtain the crude product. Finally, the crude product was purified by fast column chromatography.

References[1] Journal of Organic Chemistry, 2000, vol. 65, # 26, p. 9143 - 9151
[2] Journal of Medicinal Chemistry, 1998, vol. 41, # 12, p. 1997 - 2009
[3] Organic Preparations and Procedures International, 2015, vol. 47, # 3, p. 227 - 231
[4] Patent: WO2009/55674, 2009, A1. Location in patent: Page/Page column 59
[5] Journal of Medicinal Chemistry, 2012, vol. 55, # 9, p. 4189 - 4204
2-(2'-BROMOPHENOXY)PROPANE Preparation Products And Raw materials
Raw materials2-Bromophenol-->2-Bromopropane-->Potassium carbonate-->Sodium iodide-->Ethanol
Tag:2-(2'-BROMOPHENOXY)PROPANE(701-07-5) Related Product Information
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