Product

TRANS-1-PROPEN-1-YLBORONIC ACID

CAS No.：7547-97-9

Other grades of this product :

TRANS-1-PROPEN-1-YLBORONIC ACID Basic information

Product Name:	TRANS-1-PROPEN-1-YLBORONIC ACID
Synonyms:	TRANS-1-PROPEN-1-YLBORONIC ACID;[(1E)-prop-1-en-1-yl]boronic acid;Prop-1-en-1-ylboronic acid;(E)-prop-1-en-1-ylboronic acid;trans-1-Propen-1-ylboronic acid >=95.0%;(E)-1-propen-1-yl-boronicacid;(E)-Prop-1-enylboronic acid;trans-1-Propeneboronic acid
CAS:	7547-97-9
MF:	C3H7BO2
MW:	85.9
EINECS:	200-258-5
Product Categories:	BoronicAcids;Boric Acid\| Boric Acid Ester\| Potassium Trifluoroborate;blocks;Alkenyl;Boronic Acids;Boronic Acids and Derivatives
Mol File:	7547-97-9.mol

TRANS-1-PROPEN-1-YLBORONIC ACID Chemical Properties

Melting point	123-127 °C(lit.)
Boiling point	175.6±23.0 °C(Predicted)
density	0.972 g/cm3(Temp: 19 °C)
storage temp.	2-8°C
solubility	Chloroform (Very Slightly, Heated), Methanol (Very Slightly)
form	Solid
pka	9.80±0.43(Predicted)
color	Pale Beige

Safety Information

WGK Germany	3
HS Code	2931900090

MSDS Information

TRANS-1-PROPEN-1-YLBORONIC ACID Usage And Synthesis

Uses

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

TRANS-1-PROPEN-1-YLBORONIC ACID Preparation Products And Raw materials

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