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1,3,5-Phenyltriboronic acid, tris(pinacol) ester

ALDRICH/900989 - ≥97%

Synonym: 1,3,5-Tris(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene

CAS Number: 365564-05-2
Empirical Formula (Hill Notation): C24H39B3O6
Molecular Weight: 456.00
MDL Number: MFCD17167305
Linear Formula: C24H39B3O6
Product Type: Chemical
Catalog Number PKG Qty. Price Quantity
45-900989-1G 1 g
 $100.00
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This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: 900989-1G.

 

assay ≥97%
form powder or crystals
InChI 1S/C24H39B3O6/c1-19(2)20(3,4)29-25(28-19)16-13-17(26-30-21(5,6)22(7,8)31-26)15-18(14-16)27-32-23(9,10)24(11,12)33-27/h13-15H,1-12H3
InChI key VKOLBYNBPONPAE-UHFFFAOYSA-N
mp 286-287 °C
Quality Level 100 
SMILES string CC1(C)OB(OC1(C)C)C2=CC(B3OC(C)(C)C(C)(C)O3)=CC(B4OC(C)(C)C(C)(C)O4)=C2
Application: 1,3,5-Phenyltriboronic acid, tris(pinacol) ester can undergo Suzuki–Miyaura cross-coupling polycondensation reaction with 4,7-dibromobenzo[c][1,2,5]thiadiazole to afford conjugated polybenzothiadiazoles. It may also be used as a crosslinker for synthesizing conjugated microporous polymer (CMP) nanoparticles. This product was previously listed as BML00299.
Other Notes: Molecular engineering of conjugated polybenzothiadiazoles for enhanced hydrogen production by photosynthesis 

Conjugated microporous polymer nanoparticles with enhanced dispersibility and water compatibility for photocatalytic applications 
RIDADR NONH for all modes of transport
WGK Germany WGK 3
Flash Point(F) Not applicable
Flash Point(C) Not applicable
Purity ≥97%
mp 286-287 °C
UNSPSC 12352106

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