Name: | 2-FLUOROPHENYLBORONIC ACID |
CAS: | 1993-03-9 ;1193-03-9 ;34-03-7 |
Synonyms: | 2-FLUOROPHENYL BORONIC ACID ; BENZENEBORONIC ACID, O-FLUORO- ; BORONIC ACID, (2-FLUOROPHENYL)- ; O-FLUORO-BENZENEBORONIC ACID ; 2-FLUOROBENZENEBORONIC ACID ; BORONIC ACID, B-(2-FLUOROPHENYL)- ; O-FLUOROPHENYLBORONIC ACID ; B-(2-FLUOROPHENYL)-BORONIC ACID ; 2-FLUOROPHENYLBORONIC ACID(I) ; 2-FLUOROPHENYLBORONIC ACID ; (2-FLUOROPHENYL)BORANEDIOL ; 4-PIPERIDINAMINE,1-METHYL-, HYDROCHLORIDE (1:2) |
MDL.: | MFCD00674013 |
H bond acceptor: | 2 |
H bond donor: | 2 |
Smile: | B(c1ccccc1F)(O)O |
InChi: | InChI=1S/C6H6BFO2/c8-6-4-2-1-3-5(6)7(9)10/h1-4,9-10H |
InChiKey: | InChIKey=QCSLIRFWJPOENV-UHFFFAOYSA-N |
Property |
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Melting Point: | 101-110 DEG C(LIT) |
Comments: | APPLICATION: REACTANT FOR: PREPARATION OF PHENYLBORONIC CATECHOL ESTERS AS PROMISING ANION RECEPTORS FOR POLYMER ELECTROLYTES. DIASTEREOSELECTIVE SYNTHESIS OF TRISUBSTITUTED ALLYLIC ALCOHOLS VIA RHODIUM-CATALYZED ARYLATION. SITE-SELECTIVE SUZUKI-MIYAURA ARYLATION REACTIONS. RH-CATALYZED ENANTIOSELECTIVE ADDITION REACTIONS. RHODIUM- AND PALLADIUM-CATALYZED SUBSTITUTION REACTIONS APPLICATION: USED FOR THE PREPARATION OF BIOLOGICALLY ACTIVE BIPHENYLS AND ARYLBORON DIFLUORIDE LEWIS ACIDS OTHER NOTES: CONTAINS VARYING AMOUNTS OF ANHYDRIDE UNSPSC: 12352103 WGK: 3 |
Safety information |
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WGK Germany: | 3 |
2-FLUOROPHENYLBORONIC ACID
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