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4-Bromo-1-chloro-2-(4-methoxy-benzyl)-benzene

Base Information Edit
  • Chemical Name:4-Bromo-1-chloro-2-(4-methoxy-benzyl)-benzene
  • CAS No.:333361-51-6
  • Molecular Formula:C14H12BrClO
  • Molecular Weight:0.00000
  • Hs Code.:
  • Mol file:333361-51-6.mol
4-Bromo-1-chloro-2-(4-methoxy-benzyl)-benzene

Synonyms:

Suppliers and Price of 4-Bromo-1-chloro-2-(4-methoxy-benzyl)-benzene
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • 4-Bromo-1-chloro-2-[(4-methoxyphenyl)methyl]benzene
  • 2.5g
  • $ 690.00
  • TRC
  • 4-Bromo-1-chloro-2-[(4-methoxyphenyl)methyl]benzene
  • 1g
  • $ 285.00
Total 14 raw suppliers
Chemical Property of 4-Bromo-1-chloro-2-(4-methoxy-benzyl)-benzene Edit
Chemical Property:
  • Boiling Point:379.8±32.0 °C(Predicted) 
  • PSA:0.00000 
  • Density:1.410±0.06 g/cm3(Predicted) 
  • LogP:0.00000 
  • Solubility.:Dichloromethane; Ethyl Acetate 
Purity/Quality:

99%, *data from raw suppliers

4-Bromo-1-chloro-2-[(4-methoxyphenyl)methyl]benzene *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses 4-Bromo-1-chloro-2-[(4-methoxyphenyl)methyl]benzene is an intermediate in synthesizing Dapagliflozin-D5 (D185372), a labelled analogue of Dapagliflozin (D185370), which is a selective sodium-glucose cotransporter-2 inhibitor that reduces renal glucose reabsorption and is used to treat patients with type 2 diabetes.
Technology Process of 4-Bromo-1-chloro-2-(4-methoxy-benzyl)-benzene

There total 4 articles about 4-Bromo-1-chloro-2-(4-methoxy-benzyl)-benzene 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:
Guidance literature:
With triethylsilane; boron trifluoride diethyl etherate; In dichloromethane; acetonitrile; at 0 - 20 ℃; for 2.33333h; Inert atmosphere;
Guidance literature:
Multi-step reaction with 3 steps
1.1: oxalyl dichloride; N,N-dimethyl-formamide / dichloromethane / 10 h / 20 °C
2.1: aluminum (III) chloride / dichloromethane / 1 h / -5 - 20 °C / Inert atmosphere
2.2: 2 h / -5 - 0 °C / Inert atmosphere
3.1: aluminum (III) chloride; sodium tetrahydroborate / tetrahydrofuran / 18 h / 5 - 20 °C / Inert atmosphere
With aluminum (III) chloride; sodium tetrahydroborate; oxalyl dichloride; N,N-dimethyl-formamide; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jm401780b
Guidance literature:
Multi-step reaction with 2 steps
1.1: aluminum (III) chloride / dichloromethane / 1 h / -5 - 20 °C / Inert atmosphere
1.2: 2 h / -5 - 0 °C / Inert atmosphere
2.1: aluminum (III) chloride; sodium tetrahydroborate / tetrahydrofuran / 18 h / 5 - 20 °C / Inert atmosphere
With aluminum (III) chloride; sodium tetrahydroborate; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jm401780b
Refernces Edit
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