Welcome to LookChem.com Sign In|Join Free
  • or

Encyclopedia

2-(Dibenzo[b,e]borinin-5(10h)-yloxy)ethanamine

Base Information Edit
  • Chemical Name:2-(Dibenzo[b,e]borinin-5(10h)-yloxy)ethanamine
  • CAS No.:7147-07-1
  • Molecular Formula:C15H16BNO
  • Molecular Weight:237.109
  • Hs Code.:
  • NSC Number:54026
  • DSSTox Substance ID:DTXSID90288077
  • Wikidata:Q82024352
  • Mol file:7147-07-1.mol
2-(Dibenzo[b,e]borinin-5(10h)-yloxy)ethanamine

Synonyms:7147-07-1;2-(dibenzo[b,e]borinin-5(10h)-yloxy)ethanamine;NSC54026;DTXSID90288077;NSC-54026

Suppliers and Price of 2-(Dibenzo[b,e]borinin-5(10h)-yloxy)ethanamine
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
Total 1 raw suppliers
Chemical Property of 2-(Dibenzo[b,e]borinin-5(10h)-yloxy)ethanamine Edit
Chemical Property:
  • Vapor Pressure:2.38E-05mmHg at 25°C 
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:3
  • Exact Mass:237.1324943
  • Heavy Atom Count:18
  • Complexity:251
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:B1(C2=CC=CC=C2CC3=CC=CC=C31)OCCN
Technology Process of 2-(Dibenzo[b,e]borinin-5(10h)-yloxy)ethanamine

There total 7 articles about 2-(Dibenzo[b,e]borinin-5(10h)-yloxy)ethanamine 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:
boric acid tributyl ester; 2-bromo-1-(2-bromobenzyl)-4-methylbenzene; With iodine; magnesium; In tetrahydrofuran; at 20 ℃; for 73h; Inert atmosphere;
ethanolamine; In ethyl acetate; at 20 ℃; Inert atmosphere;
DOI:10.1002/chem.202003319
Guidance literature:
With hydrogenchloride; In tetrahydrofuran; benzene; (Ar); to THF soln. of Grignard reagent was added boron compd. in benzene and react. quenched after 15 min with aq. HCl, soln. was extd. with ether, dried (Na2SO4) exts. evapd. in vac. and residual oil treated with ethanolamine; after 5 min mixt. was poured into ether/water (1:1), pptd. product was filtered off and recrystd. from EtOH;
DOI:10.1021/ja00319a032
Guidance literature:
Multi-step reaction with 3 steps
1.1: isopropylmagnesium chloride / tetrahydrofuran / 1.5 h / -20 °C / Inert atmosphere
1.2: 0.75 h / -20 - -15 °C / Inert atmosphere
2.1: trifluoroacetic acid / dichloromethane / 0.08 h / 0 °C
2.2: 16 h / 0 - 20 °C
3.1: iodine; magnesium / tetrahydrofuran / 73 h / 20 °C / Inert atmosphere
3.2: 20 °C / Inert atmosphere
With iodine; isopropylmagnesium chloride; magnesium; trifluoroacetic acid; In tetrahydrofuran; dichloromethane;
DOI:10.1002/chem.202003319
Post RFQ for Price