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Home > Encyclopedia > Allylboronic acid pinacol ester

Allylboronic acid pinacol ester

Allylboronic acid pinacol ester structure

Allylboronic acid pinacol ester 

structure
  • CAS No:

    72824-04-5

  • Formula:

    C9H17BO2

  • Chemical Name:

    Allylboronic acid pinacol ester

  • Synonyms:

    2-(Prop-2-en-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, 2-Allyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane;Allylboronic acid pinacol ester 97%;Allylboronic acid pinacol ester2-Allyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane;1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-(2-propen-1-yl)-;(2-Propen-1-yl)-boronic acid pinacol ester;Allyl pinacol boronate Pinacolyl 2-propenylboronate;3-Hydroxy-2,3-dimethylbutan-2-yl hydrogen allylboronate;Allylboronic acid picol ester

  • Categories:

    Pharmaceutical Intermediates  >  Respiratory Tract

Description

Clear corless liquid

Allylboronic acid pinacol ester Basic Attributes

168.04

168.132156

4244068

-0

DTXSID70376784

29310095

Characteristics

18.5

2.26460

Clear colorless Liquid

0.9±0.1 g/cm3

50-53 °C5 mm Hg(lit.)

115 °F

1.424

Not miscible or difficult to mix in water.

Refrigerator

Safety Information

3

UN 1993 3/PG 3

3

10-36/37/38

26-36

Xi

Irritant

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, P501

H226

|Warning|H226 (97.96%): Flammable liquid and vapor [Warning Flammable liquids]|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|Aggregated GHS information provided by 49 companies from 9 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Allylboronic acid pinacol ester Use and Manufacturing

Reagent used for• ;Palladium-catalyzed Suzuki-Miyaura cross-coupling reactions and olefin metathesis1 • ;Intermolecular radical additions2 • ;Allylboration of aldehydes catalyzed by chiral spirobiindane diol (SPINOL) based phosphoric acids3 • ;Cobalt-catalyzed regioselective hydrovinylation of dienes with alkenes4 • ;Nucleic acid-templated energy transfer leading to a photorelease reaction5 • ;Stereoselective indium-catalyzed Hosomi-Sakurai reactions6 Reagent used in Preparation of• ;Cyclic sulfone hydroxyethylamines as BACE1 inhibitors for reduction o

Computed Properties

Molecular Weight:168.04
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:168.1321599
Monoisotopic Mass:168.1321599
Topological Polar Surface Area:18.5
Heavy Atom Count:12
Complexity:171
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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