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
Canonical 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
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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