Cyclopentylboronic Acid
Product Information
Molecular Formula
C5H11O2B
Molecular Weight
113.95
Description
Reactant involved in: Cross coupling reactions with quinones or aromatic amines; Arylation and alkylation of diphenylisoxazole; Ruphos-mediated Suzuki cross coupling reactions.
Synonyms
cyclopentylboronic acid; cyclopentylboronic acid
IUPAC Name
cyclopentylboronic acid
SMILES
B(C1CCCC1)(O)O
InChI
InChI=1S/C5H11BO2/c7-6(8)5-3-1-2-4-5/h5,7-8H,1-4H2
InChI Key
VTTDFSNKIMAQTB-UHFFFAOYSA-N
Boiling Point
235 °C at 760 mmHg
Melting Point
126 °C (dec.) (lit.)
Flash Point
Not applicable
Purity
≥ 95 %
Density
1.03 g/cm3
LogP
0.40340
Safety Information
Precautionary Statement
P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P305+P351+P338, P312, P321, P322, P330, P332+P313, P337+P313, P362, P363, P403+P233, P405, and P501
Signal Word
Warning
Computed Properties
Hydrogen Bond Donor Count
2
Hydrogen Bond Acceptor Count
2
Rotatable Bond Count
1
Exact Mass
114.0852098 g/mol
Monoisotopic Mass
114.0852098 g/mol
Topological Polar Surface Area
40.5Ų
Heavy Atom Count
8
Formal Charge
0
Complexity
68.8
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes
Patents
| Publication Number | Title | Priority Date |
|---|---|---|
| CN-113801037-A | One-step method for preparing C-N coupling product from nitroaromatic and alkyl or phenyl boric acid | 2021-08-24 |
| KR-20220018307-A | Novel compound and organic light emitting device comprising the same | 2020-08-06 |
| JP-2022021687-A | Method for Producing N-Substituted (Meta) Acrylamide | 2020-07-22 |
| WO-2022020150-A1 | Methods of extending lifespan by administering ferroptosis inhibitors | 2020-07-21 |
| WO-2022003712-A1 | Quinazolinones derivatives for treatment of non-alcoholic fatty liver disease, preparation and use thereof | 2020-06-29 |
| WO-2021182557-A1 | Polarizing film and method for manufacturing same | 2020-03-13 |
| CN-112778337-A | 3,6 diazabicyclo [3.1.1] heptane derivatives as RET kinase inhibitors | 2019-11-08 |
| WO-2021088911-A1 | 3,6-diazabicyclo[3.1.1]heptane derivative as ret kinase inhibitor | 2019-11-08 |
| JP-2021031401-A | Compounds having a fluorene skeleton and methods for producing them | 2019-08-19 |
| WO-2021020349-A1 | Polarizing film and method for producing same | 2019-07-29 |
Literatures
| PMID | Publication Date | Title | Journal |
|---|---|---|---|
| 22322664 | 2012-03-28 | Mechanism and optimisation of the homoboroproline bifunctional catalytic asymmetric aldol reaction: Lewis acid tuning through in situ esterification | Organic & biomolecular chemistry |
