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(E)-2-(3-Chlorostyryl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Base Information
  • Chemical Name:(E)-2-(3-Chlorostyryl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • CAS No.:871125-84-7
  • Molecular Formula:C14H18 B Cl O2
  • Molecular Weight:264.56
  • Hs Code.:2934999090
  • European Community (EC) Number:866-153-8
  • DSSTox Substance ID:DTXSID60584790
  • Wikidata:Q82476513
  • Mol file:871125-84-7.mol
(E)-2-(3-Chlorostyryl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Synonyms:871125-84-7;(E)-2-(3-Chlorostyryl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane;E-2-(3-Chlorophenyl)vinylboronic acid, pinacol ester;trans-2-(3-Chlorophenyl)vinylboronic acid pinacol ester;2-[(E)-2-(3-Chlorophenyl)ethenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane;E-2-(3-Chlorophenyl)vinylboronic acid,pinacol ester;1377152-51-6;2-(3-Chlorostyryl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane;MFCD08276867;SCHEMBL692214;SCHEMBL692215;DTXSID60584790;NZBKTAJNGYXYSQ-CMDGGOBGSA-N;AKOS022172759;GS-6175;EN300-212607;H10472;EN300-7353784;A862837;Z2315585634;trans-2-(3-Chlorophenyl)vinylboronic acid pinacol ester, 97%;2-[(E)-2-(3-Chloro-phenyl)-vinyl]-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane;2-[2-(3-CHLOROPHENYL)ETHENYL]-4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLANE

Suppliers and Price of (E)-2-(3-Chlorostyryl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Supply Marketing:
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
  • E-2-(3-Chlorophenyl)vinylboronicacid,pinacolester
  • 25mg
  • $ 45.00
  • Sigma-Aldrich
  • trans-2-(3-Chlorophenyl)vinylboronic acid pinacol ester 97%
  • 1g
  • $ 189.00
  • Sigma-Aldrich
  • trans-2-(3-Chlorophenyl)vinylboronic acid pinacol ester 97%
  • 5g
  • $ 595.00
  • Crysdot
  • (E)-2-(3-Chlorostyryl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 95+%
  • 5g
  • $ 447.00
  • Atlantic Research Chemicals
  • 2-[2-(3-Chlorophenyl)ethenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 95%
  • 1gm:
  • $ 201.47
  • American Custom Chemicals Corporation
  • TRANS-2-(3-CHLOROPHENYL)VINYLBORONIC ACID PINACOL ESTER 95.00%
  • 1G
  • $ 345.45
  • Alichem
  • (E)-2-(3-Chlorostyryl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 5g
  • $ 368.65
Total 14 raw suppliers
Chemical Property of (E)-2-(3-Chlorostyryl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Chemical Property:
  • Vapor Pressure:0.00147mmHg at 25°C 
  • Refractive Index:n20/D 1.536  
  • Boiling Point:138-140 °C0.9-1.0 mm Hg  
  • Flash Point:>230 °F  
  • PSA:18.46000 
  • Density:1.049 g/mL at 25 °C  
  • LogP:3.98460 
  • Storage Temp.:2-8°C 
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:2
  • Exact Mass:264.1088377
  • Heavy Atom Count:18
  • Complexity:312
Purity/Quality:

97% *data from raw suppliers

E-2-(3-Chlorophenyl)vinylboronicacid,pinacolester *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:B1(OC(C(O1)(C)C)(C)C)C=CC2=CC(=CC=C2)Cl
  • Isomeric SMILES:B1(OC(C(O1)(C)C)(C)C)/C=C/C2=CC(=CC=C2)Cl
  • Uses E-2-(3-Chlorophenyl)vinylboronic acid, pinacol ester trans-2-(3-Chlorophenyl)vinylboronic acid pinacol ester can be used as a reactant: To prepare aryl derivatives by C?C bond formation via palladium-catalyzed Suzuki?Miyaura reaction. In the diastereoselective synthesis of alkenes via K3PO4-promoted transition metal-free nucleophilic substitution of unactivated alkyl triflates. To synthesize (3-chlorophenyl)cyclopropyl boronic acid pinacol ester by reacting with diazomethane.
Technology Process of (E)-2-(3-Chlorostyryl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

There total 6 articles about (E)-2-(3-Chlorostyryl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 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 2.9 weight% Cu(II) loaded porous coordination network-222 nanoparticles; In ethanol; water; at 80 ℃; regioselective reaction; Sealed tube;
DOI:10.1016/j.jcat.2021.06.013
Guidance literature:
With bis(cyclopentadienyl)dihydrozirconium; In toluene; at 25 ℃; Inert atmosphere; Glovebox;
DOI:10.1002/anie.201908931
Guidance literature:
With dibutylmagnesium; In n-heptane; toluene; at 80 ℃; for 18h; regioselective reaction; Inert atmosphere;
DOI:10.1002/anie.201902188
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