2-(2-Fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Base Information

Chemical Name:2-(2-Fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
CAS No.:876062-39-4
Molecular Formula:C₁₂H₁₆BFO₂
Molecular Weight:222.067
Hs Code.:2934999090
European Community (EC) Number:812-088-5
DSSTox Substance ID:DTXSID20478863
Nikkaji Number:J2.278.415C
Wikidata:Q72475748
Mol file:876062-39-4.mol

Synonyms:876062-39-4;2-(2-Fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane;2-FLUOROPHENYLBORONIC ACID, PINACOL ESTER;2-Fluorophenylboronic acid pinacol ester;MFCD05663874;1,3,2-DIOXABOROLANE, 2-(2-FLUOROPHENYL)-4,4,5,5-TETRAMETHYL-;2-(2-fluoro-phenyl)-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane;SCHEMBL9786;(2-FLUOROPHENYL)BORONIC ACID PINACOL ESTER;DTXSID20478863;RZYXBJMVAFMMLQ-UHFFFAOYSA-N;AKOS004115185;AB21994;CS-W023174;AM808075;AS-18067;SY051378;F1085;Y10112;EN300-1425761;A862507;2-fluorophenylboronic acid, pinacol ester, AldrichCPR;Z1336745114;1-Fluoro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene;2-(2-Fluorophenyl)-4 pound not4 pound not5 pound not5-tetramethyl-1 pound not3 pound not2-dioxaborolane

Suppliers and Price of 2-(2-Fluorophenyl)-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
2-Fluorophenylboronicacid,pinacolester
250mg
$ 55.00

TCI Chemical
2-(2-Fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane >98.0%(GC)(T)
5g
$ 131.00

TCI Chemical
2-(2-Fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane >98.0%(GC)(T)
25g
$ 393.00

SynQuest Laboratories
2-(2-Fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
10 g
$ 944.00

J&W Pharmlab
2-(2-Fluoro-phenyl)-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane 96%
5g
$ 105.00

J&W Pharmlab
2-(2-Fluoro-phenyl)-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane 96%
1g
$ 34.00

J&W Pharmlab
2-(2-Fluoro-phenyl)-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane 96%
25g
$ 340.00

Crysdot
2-(2-Fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 97%
25g
$ 293.00

Crysdot
2-(2-Fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 97%
1g
$ 21.00

Crysdot
2-(2-Fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 97%
5g
$ 94.00

Total 44 raw suppliers

Chemical Property of 2-(2-Fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Chemical Property:

Vapor Pressure:0.005mmHg at 25°C
Refractive Index:1.4830 to 1.4870
Boiling Point:284.63oC at 760 mmHg
Flash Point:125.94oC
PSA：18.46000
Density:1.058g/cm3
LogP:2.12490
Storage Temp.:2-8°C
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:222.1227381
Heavy Atom Count:16
Complexity:252

Purity/Quality:

97% ^*data from raw suppliers

2-Fluorophenylboronicacid,pinacolester ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:Xn
Statements: 22

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:B1(OC(C(O1)(C)C)(C)C)C2=CC=CC=C2F

Technology Process of 2-(2-Fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

There total 14 articles about 2-(2-Fluorophenyl)-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:

Reference yield: 61.0%

: 876062-39-4
2-(2-fluorophenyl)-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane

Guidance literature:: In diethyl ether; at 20 ℃; for 4h;

Reference yield:

: 462-06-6
fluorobenzene

: 73183-34-3
bis(pinacol)diborane

: 876062-39-4
2-(2-fluorophenyl)-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane

: 936618-92-7
2-(3-fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Guidance literature:: With (^iPrPNP)CoCH₂SiMe₃; In neat (no solvent); at 80 ℃; for 24h; Overall yield = 95 %; Overall yield = 0.049 g; Inert atmosphere; Glovebox;
DOI:10.1021/ja500712z