1-(2-bromoethoxy)-2-isopropylbenzene

Base Information

• Chemical Name: 1-(2-bromoethoxy)-2-isopropylbenzene
• CAS No.: 3245-44-1
• Molecular Formula: C11H15BrO
• Molecular Weight: 243.143
• Hs Code.: 2909309090
• Mol file: 3245-44-1.mol

Synonyms:1-(2-bromoethoxy)-2-isopropylbenzene;UKRORGSYN-BB BBV-074985;1-(2-bromoethoxy)-2-isopropylbenzene(SALTDATA: FREE)

Chemical Property of 1-(2-bromoethoxy)-2-isopropylbenzene

Chemical Property:

• Vapor Pressure: 0.00336mmHg at 25°C
• Boiling Point: 291.6°C at 760 mmHg
• Flash Point: 115.3°C
• PSA: 9.23000
• Density: 1.258g/cm³
• LogP: 3.58370

Purity/Quality:

99% ^*data from raw suppliers

1-(2-Bromo-ethoxy)-2-isopropyl-benzene ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of 1-(2-bromoethoxy)-2-isopropylbenzene

There total 2 articles about 1-(2-bromoethoxy)-2-isopropylbenzene which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 74.0%

2-(1-methylethyl)phenol (88-69-7) + ethylene dibromide (106-93-4) → 1-(2-bromoethoxy)-2-(propan-2-yl)benzene (3245-44-1)

Guidance literature:

With potassium carbonate; potassium iodide; In acetone; at 60 ℃;

DOI:10.1016/j.bmc.2015.11.041

Reference yield: 62.0%

→ 1-(2-bromoethoxy)-2-(propan-2-yl)benzene (3245-44-1)

Guidance literature:

With sodium hydroxide; In water; at 130 ℃; for 16h;

Reference yield: 72.0%

1-(2-bromoethoxy)-2-(propan-2-yl)benzene (3245-44-1) + (piperidin-4-yl)carbamic acid tert-butyl ester (73874-95-0) → t-butyl (1-{[2-(propan-2-yl)phenoxy]ethyl}piperidin-4-yl)carbamate

Guidance literature:

With potassium carbonate; potassium iodide; In acetone; for 48h; Reflux;

DOI:10.1016/j.bmc.2015.11.041

upstream raw materials:

2-(1-methylethyl)phenol

ethylene dibromide

Downstream raw materials:

N-<2-(2-Isopropyl-phenoxy)-aethyl>-3-(2-methoxy-phenoxy)-propylamin

C₂₂H₃₀N₂O₂S

2,5-dimethoxy-N-[(1-{2-[2-(propan-2-yl)phenoxy]ethyl}piperidin-4-yl)methyl]benzenesulfonamide

C₂₅H₃₄N₂O₃

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