2-Pyrrolylboronic acid

Base Information

Chemical Name:2-Pyrrolylboronic acid
CAS No.:763120-43-0
Molecular Formula:C4H6 B N O2
Molecular Weight:110.908
Hs Code.:2933990090
DSSTox Substance ID:DTXSID80400625
Nikkaji Number:J2.130.564B
Wikidata:Q72505737
Mol file:763120-43-0.mol

Synonyms:2-Pyrrolylboronic acid;763120-43-0;1H-pyrrol-2-ylboronic Acid;PYRROLE-2-BORONIC ACID;Boronic acid, 1H-pyrrol-2-yl-;(1H-pyrrol-2-yl)boronic acid;2-Pyrrolylboronicacid;SCHEMBL488858;1H-pyrrol-2-yl-2-boronic acid;DTXSID80400625;WADSQZHEAXPENM-UHFFFAOYSA-N;MFCD03095055;AKOS006278865;AB13435;CS-0377022;FT-0691108;A838669

Suppliers and Price of 2-Pyrrolylboronic acid

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

Crysdot
2-Pyrrolylboronicacid 95+%
1g
$ 580.00

American Custom Chemicals Corporation
2-PYRROLYL BORONIC ACID 95.00%
1G
$ 975.45

Alichem
Pyrrole-2-boronicacid
10g
$ 3098.53

Alichem
Pyrrole-2-boronicacid
1g
$ 938.40

Total 28 raw suppliers

Chemical Property of 2-Pyrrolylboronic acid

Chemical Property:

Vapor Pressure:1.1E-05mmHg at 25°C
Boiling Point:356oC at 760 mmHg
PKA:8.85±0.53(Predicted)
Flash Point:169.1oC
PSA：56.25000
Density:1.28g/cm3
LogP:-1.30550
Storage Temp.:Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:111.0491586
Heavy Atom Count:8
Complexity:78.4

Purity/Quality:

98% ^*data from raw suppliers

2-Pyrrolylboronicacid 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:
Statements: 36/37/38
Safety Statements: 26-36/37/39

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:B(C1=CC=CN1)(O)O

Technology Process of 2-Pyrrolylboronic acid

There total 1 articles about 2-Pyrrolylboronic acid 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: 13.0%

: 16851-82-4
N-phenylsulfonylpyrrole

: 763120-43-0
pyrrole-2-boronic acid

Guidance literature:: N-phenylsulfonylpyrrole; With isopropylmagnesium bromide; diisopropylamine; In tetrahydrofuran; at 50 ℃; for 16h;

With Trimethyl borate; In tetrahydrofuran; at 50 ℃;
DOI:10.1021/ol036288p

Reference yield: 83.3%

: 4-bromo-N-(inden-5-yl)benzenesulfonamide

: 763120-43-0
pyrrole-2-boronic acid

: C₁₉H₁₆N₂O₂S

Guidance literature:: With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In tetrahydrofuran; Inert atmosphere; Reflux;

Reference yield: 58.0%

: 3-(3-(4-(2-bromo-4-fluorophenyl)piperazin-1-yl)propyl)-5-fluoro-1H-indole

: 763120-43-0
pyrrole-2-boronic acid

: C₂₅H₂₆F₂N₄*ClH

Guidance literature:: 3-(3-(4-(2-bromo-4-fluorophenyl)piperazin-1-yl)propyl)-5-fluoro-1H-indole; pyrrole-2-boronic acid; With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; sodium carbonate; In 1,4-dioxane; water; at 80 ℃; for 12h; Inert atmosphere;

With hydrogenchloride; In ethyl acetate;