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3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)quinoline

Base Information Edit
  • Chemical Name:3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)quinoline
  • CAS No.:171364-85-5
  • Molecular Formula:C15H18BNO2
  • Molecular Weight:255.124
  • Hs Code.:2933499090
  • European Community (EC) Number:626-347-3
  • DSSTox Substance ID:DTXSID00445795
  • Nikkaji Number:J1.768.873A
  • Wikidata:Q72505822
  • Mol file:171364-85-5.mol
3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)quinoline

Synonyms:171364-85-5;3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)quinoline;Quinoline-3-boronic acid pinacol ester;3-Quinolineboronic acid pinacol ester;Quinoline-3-boronic acid pinacolate;Quinoline-3-boronic acid, pinacol ester;QUINOLINE, 3-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)-;3-(tetramethyl-1,3,2-dioxaborolan-2-yl)quinoline;MFCD05155218;AKOS BRN-1143;SCHEMBL167417;DTXSID00445795;ARRJAONCYUAPJR-UHFFFAOYSA-N;BCP26740;3-quinoline-boronic acid pinacol ester;AKOS004114766;AB21547;AM86067;CS-W020549;GS-6488;3-Quinolineboronic acid pinacol ester, 95%;3-Quinolineboronic acid pinacol ester, 97%;FT-0690024;T3180;A22838;EN300-212559;QUINOLIN-3-YLBORONIC ACID PINACOL ESTER;J-010718;Z1336745105;2-(3-Quinolyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane;4,4,5,5-Tetramethyl-2-(3-quinolyl)-1,3,2-dioxaborolane;3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-quinoline;3-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)quinoline;3-(4,4,5,5-tetramethyl-1,3,2,-dioxaborolan-2-yl)quinoline

Suppliers and Price of 3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)quinoline
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
  • Usbiological
  • Quinoline-3-boronic acid pinacol ester
  • 1g
  • $ 435.00
  • TRC
  • 3-Quinolineboronic acid pinacol ester
  • 5g
  • $ 225.00
  • TCI Chemical
  • 3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)quinoline >98.0%(GC)(T)
  • 5g
  • $ 300.00
  • TCI Chemical
  • 3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)quinoline >98.0%(GC)(T)
  • 1g
  • $ 95.00
  • Sigma-Aldrich
  • 3-Quinolineboronic acid pinacol ester 95%
  • 1g
  • $ 80.20
  • Sigma-Aldrich
  • 3-Quinolineboronic acid pinacol ester 95%
  • 5g
  • $ 311.00
  • Medical Isotopes, Inc.
  • 3-Quinolineboronic acid pinacol ester
  • 1 g
  • $ 355.00
  • Matrix Scientific
  • Quinoline-3-boronic acid pinacol ester 95+%
  • 5g
  • $ 588.00
  • Matrix Scientific
  • Quinoline-3-boronic acid pinacol ester 95+%
  • 1g
  • $ 227.00
  • Crysdot
  • 3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)quinoline 97%
  • 5g
  • $ 157.00
Total 62 raw suppliers
Chemical Property of 3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)quinoline Edit
Chemical Property:
  • Vapor Pressure:0mmHg at 25°C 
  • Melting Point:56-60 °C(lit.) 
  • Refractive Index:1.559 
  • Boiling Point:386.468 °C at 760 mmHg 
  • PKA:5.12±0.12(Predicted) 
  • Flash Point:187.53 °C 
  • PSA:31.35000 
  • Density:1.101 g/cm3 
  • LogP:2.53400 
  • Storage Temp.:Refrigerator 
  • Solubility.:Chloroform (Slightly), Ethyl Acetate (Slightly) 
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:1
  • Exact Mass:255.1430590
  • Heavy Atom Count:19
  • Complexity:329
Purity/Quality:

98% *data from raw suppliers

Quinoline-3-boronic acid pinacol ester *data from reagent suppliers

Safty Information:
  • Pictogram(s): IrritantXi 
  • Hazard Codes:Xi 
  • Statements: 36/37/38 
  • Safety Statements: 26-36 
MSDS Files:
Useful:
  • Canonical SMILES:B1(OC(C(O1)(C)C)(C)C)C2=CC3=CC=CC=C3N=C2
  • Uses 3-Quinolineboronic Acid Pinacol Ester is used as a reagent in the synthesis of 11-(pyridinylphenyl)steroids which is a novel class of mixed progesterone agonists / antagonists.
Technology Process of 3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)quinoline

There total 11 articles about 3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)quinoline 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 potassium acetate; In isopropyl alcohol; at 82 ℃; for 2h;
DOI:10.1002/cctc.201301035
Guidance literature:
Guidance literature:
With tert.-butylnitrite; In acetonitrile; at 80 ℃; for 2h;
DOI:10.1021/jo3018878
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