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3-CHLORO-4-ISOPROPOXYPHENYLBORONIC ACID

3-CHLORO-4-ISOPROPOXYPHENYLBORONIC ACID Struktur
480438-56-0
CAS-Nr.
480438-56-0
Englisch Name:
3-CHLORO-4-ISOPROPOXYPHENYLBORONIC ACID
Synonyma:
3-Chloro-4-isopropoxybenzeneboronic acid;[3-chloro-4-(propan-2-yloxy)phenyl]boronic acid;3-Chloro-4-(1-methylethyl)oxyphenylboronic acid;(3-Chloro-4-isopropoxyphenyl)boronic acid - [C2206];Boronic acid, B-[3-chloro-4-(1-methylethoxy)phenyl]-;Boronic acid, [3-chloro-4-(1-methylethoxy)phenyl]- (9CI)
CBNumber:
CB7499924
Summenformel:
C9H12BClO3
Molgewicht:
214.45
MOL-Datei:
480438-56-0.mol

3-CHLORO-4-ISOPROPOXYPHENYLBORONIC ACID Eigenschaften

Schmelzpunkt:
140-145 °C(lit.)
Siedepunkt:
357.1±52.0 °C(Predicted)
Dichte
1.23±0.1 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
7.75±0.18(Predicted)
Aussehen
White to off-white Solid
InChI
InChI=1S/C9H12BClO3/c1-6(2)14-9-4-3-7(10(12)13)5-8(9)11/h3-6,12-13H,1-2H3
InChIKey
PJBWTULFEPFOEB-UHFFFAOYSA-N
SMILES
B(C1=CC=C(OC(C)C)C(Cl)=C1)(O)O

Sicherheit

WGK Germany  3
HS Code  2931900090

3-CHLORO-4-ISOPROPOXYPHENYLBORONIC ACID Chemische Eigenschaften,Einsatz,Produktion Methoden

Verwenden

Reactant for:• ;Preparation of alkyl- and aryl quinones via silver nitrate-catalyzed coupling with quinones1• ;Rhodium-catalyzed asymmetric arylation of alkenylheterocycles2• ;Stereoselective and regioselective rhodium-catalyzed carbometalation of ynamides3

3-CHLORO-4-ISOPROPOXYPHENYLBORONIC ACID Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte

3-CHLORO-4-ISOPROPOXYPHENYLBORONIC ACID Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Global( 82)Lieferanten
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  • 3-Chloro-4-(1-methylethyl)oxyphenylboronic acid
  • 3-Chloro-4-isopropoxybenzeneboronic acid
  • [3-chloro-4-(propan-2-yloxy)phenyl]boronic acid
  • Boronic acid, [3-chloro-4-(1-methylethoxy)phenyl]- (9CI)
  • Boronic acid, B-[3-chloro-4-(1-methylethoxy)phenyl]-
  • (3-Chloro-4-isopropoxyphenyl)boronic acid - [C2206]
  • 480438-56-0
  • ClC6HOCHCH3CH3
  • Aryl
  • Boronic Acids
  • Boronic Acids and Derivatives
  • Aryl Boronic Acids
  • Boronic Acids
  • Boronic Acids and Derivatives
  • Chemical Synthesis
  • Disubstituted Aryl Boronic Acids
  • Organometallic Reagents
  • BORONICACID
  • blocks
  • BoronicAcids
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