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trans-1-Propen-1-ylboronic acid

ALDRICH/576638 - ≥95.0%

Synonym: (E)-1-Propen-1-ylboronic acid; (E)-Prop-1-enylboronic acid; trans-1-Propeneboronic acid; trans-1-Propenylboronic acid; trans-Propenylboronic acid

CAS Number: 7547-97-9
Empirical Formula (Hill Notation): C3H7BO2
Molecular Weight: 85.90
MDL Number: MFCD02179501
Linear Formula: CH3CH=CHB(OH)2
Product Type: Chemical
Catalog Number PKG Qty. Price Quantity
45-576638-1G 1 g
 $1100.00
1/EA		 Add To Favorites
45-576638-5G 5 g
 $1300.00
1/EA		 Add To Favorites
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: 576638-1G

 

assay ≥95.0%
impurities ~10 wt. % cis-isomer
InChI 1S/C3H7BO2/c1-2-3-4(5)6/h2-3,5-6H,1H3/b3-2+
InChI key CBMCZKMIOZYAHS-NSCUHMNNSA-N
mp 123-127 °C (lit.)
Quality Level 100 
SMILES string [H]C(C)=C([H])B(O)O
storage temp. 2-8°C
Application: Reactant for:
• Palladium-phosphine-catalyzed Suzuki-Miyaura coupling reactions
• Cu(II)-mediated Ullmann-type coupling

Reactant for preparation of:
• Alkynylphenoxyacetic acids as DP2 receptor antagonists for treatment of allergic inflammatory diseases
• Tetrahydrobenzothiophenes as conformationally restricted enol-mimic inhibitors of type II dehydroquinase via Paal-Knorr synthesis involving Suzuki coupling
• Highly substituted benzannulated cyclooctanol derivatives by samarium diiodide-mediated cyclization
• Stereospecific dienes via nickel-catalyzed three-component reductive coupling with alkynes and enones
Application: Reactant for
• Palladium-phosphine-catalyzed Suzuki-Miyaura coupling reactions
• Cu(II)-mediated Ullmann-type coupling
• Palladium-catalyzed Sonogashira cross-coupling

Reactant for preparation of
• Alkynylphenoxyacetic acids as DP2 receptor antagonists for treatment of allergic inflammatory diseases
• Tetrahydrobenzothiophenes as conformationally restricted enol-mimic inhibitors of type II dehydroquinase via Paal-Knorr synthesis involving Suzuki coupling
• Highly substituted benzannulated cyclooctanol derivatives by samarium diiodide-mediated cyclization
• Stereospecific dienes via nickel-catalyzed three-component reductive coupling with alkynes and enones
Other Notes: Contains varying amounts of anhydride
Packaging: 1, 5 g in glass bottle
RIDADR NONH for all modes of transport
WGK Germany WGK 3
Flash Point(F) Not applicable
Flash Point(C) Not applicable
Purity ≥95.0%
mp 123-127 °C (lit.)
Storage Temp. 2-8°C
UNSPSC 12352103

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