Isopropenylboronic Acid Pinacol Ester
Product Information
Molecular Formula
C9H17O2B
Molecular Weight
168.04
Description
Reagent used for: Palladium-catalyzed Suzuki-Miyaura cross-coupling processes ; Inverse-electron-demand Diels-Alder reaction; Simmons-Smith Cyclopropanation Reaction ; Polyene cyclization ; Stereoselective aldol reactions ; Grubbs cross-metathesis reaction ; Intramolecular Suzuki-Miyaura reaction ; Stereoselective cross-metathesis ; Dipolar cycloaddition; Iodosulfonylation ; Asymmetric conjugate addition and intramolecular hydroacylation Reagent used in preparation of various therapeutic kinase and enzymatic inhibitors 9 Reagent used for; Palladium-catalyzed Suzuki-Miyaura cross-coupling reactions ; Inverse-electron-demand Diels-Alder reaction ; Simmons-Smith Cyclopropanation Reaction ; Polyene cyclization ; Stereoselective aldol reactions ; Grubbs cross-metathesis reaction ; Intramolecular Suzuki-Miyaura reaction ; Stereoselective cross-metathesis ; Dipolar cycloaddition; Iodosulfonylation ; Asymmetric conjugate addition and intramolecular hydroacylation Reagent used in preparation of various therapeutic kinase and enzymatic inhibitors.
Synonyms
4,4,5,5-tetramethyl-2-(1-methylethenyl)-1,3,2-dioxaborolane; 4,4,5,5-tetramethyl-2-prop-1-en-2-yl-1,3,2-dioxaborolane
IUPAC Name
4,4,5,5-tetramethyl-2-prop-1-en-2-yl-1,3,2-dioxaborolane
SMILES
B1(OC(C(O1)(C)C)(C)C)C(=C)C
InChI
InChI=1S/C9H17BO2/c1-7(2)10-11-8(3,4)9(5,6)12-10/h1H2,2-6H3
InChI Key
SVSUYEJKNSMKKW-UHFFFAOYSA-N
Boiling Point
47-49 °C / 9 mbar
Flash Point
107.6 °F
Purity
95 %
Density
0.894 g/mL at 25 °C
Storage
2-8 °C
Refractive Index
n20/D 1.4320
LogP
2.19390
Safety Information
Hazards
H226 - H315 - H317 - H319 - H335
Precautionary Statement
P210, P233, P240, P241, P242, P243, P261, P264, P271, P280, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P370+P378, P403+P233, P403+P235, P405, and P501
Signal Word
Warning
Computed Properties
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
2
Rotatable Bond Count
1
Exact Mass
168.1321599 g/mol
Monoisotopic Mass
168.1321599 g/mol
Topological Polar Surface Area
18.5Ų
Heavy Atom Count
12
Formal Charge
0
Complexity
193
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-114085458-A | High-strength high-toughness flame-retardant polypropylene composite material and preparation method thereof | 2021-12-08 |
| CN-114042069-A | 5-substituted pyridazine-4-amine derivative, preparation method and application | 2021-10-22 |
| CN-113666865-A | Synthetic method of 2-isopropyl-3-amino-4-methylpyridine | 2021-09-07 |
| CN-113735888-A | Synthetic method of isopropenyl pinacol borate | 2021-09-06 |
| CN-113402461-A | Method for preparing guaiazupyridine type sesquiterpene alkaloid | 2021-06-21 |
| CN-113185228-A | Processing method of aluminum silicate wall heat-insulating material | 2021-05-10 |
| EP-3915971-A1 | Phenyl-s(o)n-phenylamidines and the use thereof as fungicides | 2020-12-16 |
| CN-112266386-A | 2-chloroadenine derivative, preparation method and application | 2020-10-20 |
| WO-2022053567-A1 | Pesticidally active heterocyclic derivatives with sulfur containing substituents | 2020-09-09 |
| WO-2022053967-A1 | Heterocyclic compounds as cbp/ep300 bromodomain inhibitors | 2020-09-09 |
