88496-88-2 Buntane-2-boronic acid

Min.Order / FOB Price:Get Latest Price

1 Kilogram	FOB Price: USD 1000.0000

1 Kilogram

FOB Price: USD 1000.0000

Min.Order :1 Kilogram
Purity: 99%
Payment Terms : L/C,T/T

Keywords

88496-88-2 Buntane-2-boronic acid C4H11BO2

Quick Details

Appearance:white powder
Application:pharma
PackAge:as clients needs
ProductionCapacity:1|Metric Ton|Day
Storage:RT
Transportation:sea

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Our company was built in 2009 with an ISO certificate.In the past 6 years, we have grown up as a famous fine chemicals supplier in China and we had established stable business relationships with Samsung,LG,Merck,Thermo Fisher Scientific and so on.Our main business covers the fields below:

1.Noble Metal Catalysts (Pt.Pd...)

2.Organic Phosphine Ligands (Tert-butyl-phosphine.Cyclohexyl-phosphine...)

3.OLED intermediates (Fluorene,Carbazole,Boric acid...)

4.Customs Synthesis

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Details:

Buntane-2-boronic acid Basic information
Product Name: Buntane-2-boronic acid
Synonyms: 2-(But-2-yl)boronic acid;Butane-2-boronic acid sec-Butylboronic acid;Butane-2-boronic acid;BUNTANE-2-BORONIC ACID;sec-Butylboronic acid;n-Butane-2-boronic acid;n-Buntane-2-boronic acid;2-Butaneboronic acid
CAS: 88496-88-2
MF: C4H11BO2
MW: 101.94
EINECS:
Product Categories: Boronic Acids and Derivatives;Chemical Synthesis;Organometallic Reagents;Heterocyclic Compounds;Alkyl;Boronic Acids;Boronic Acids and Derivatives;Organoborons;Alkyl Boronic Acids;Boronic Acids
Mol File: 88496-88-2.mol
Buntane-2-boronic acid Chemical Properties
Melting point 85-89 °C
storage temp. 2-8°C
Safety Information
MSDS Information
Buntane-2-boronic acid Usage And Synthesis
Uses Reactant for:• ;Preparation of alkyl- and aryl quinones via silver nitrate-catalyzed coupling with quinones1• ;Preparation of arenes by coupling reactions with aryl bromides and chlorides in the presence of palladium complexes of a (pentaphenylferrocenyl)di(tert-butyl)phosphine2
Uses suzuki reaction
Purification Methods Purify the acid by recrystallisation from *C6H6/pet ether and dry in vacuo. [McCusker et al. J Am Chem Soc 79 5179 1957, Beilstein 4 IV 4386.]

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