9-METHOXY-9-BORABICYCLO[3.3.1]NONANE
9-METHOXY-9-BORABICYCLO[3.3.1]NONANE
  • CAS No.:38050-71-4
Other grades of this product :
9-METHOXY-9-BORABICYCLO[3.3.1]NONANE Basic information
Product Name:9-METHOXY-9-BORABICYCLO[3.3.1]NONANE
Synonyms:9-Borabicyclo[3.3.1]nonane,9-methoxy-;9-METHOXY-9-BORABICYCLO[3.3.1]NONANE;9-Methoxy-9-borabicycL;B-METHOXY-9-BBN;B-METHOXY-9-BBN, 1.0M SOLUTION IN HEXANE S;b-methoxy-9-bbn solution;8-Methoxy-9-borabicyclo[3,3,1]nonane;9- methoxy-9-borabicyclo[3.3.1]nonane 1.0M in hexanes
CAS:38050-71-4
MF:C9H17BO
MW:152.04
EINECS:253-758-1
Product Categories:
Mol File:38050-71-4.mol
9-METHOXY-9-BORABICYCLO[3.3.1]NONANE Chemical Properties
Boiling point 57-58 °C(Press: 7 Torr)
density 0.716 g/mL at 25 °C
Fp −9 °F
InChIKeyUNGDGQYONLTNJZ-UHFFFAOYSA-N
Safety Information
Hazard Codes F,Xn,N
Risk Statements 11-20/21/22-67-65-62-51/53-48/20-38
Safety Statements 16-23-36/37/39-45-62-61-36/37
RIDADR UN 1993 3/PG 2
WGK Germany 3
MSDS Information
ProviderLanguage
SigmaAldrich English
9-METHOXY-9-BORABICYCLO[3.3.1]NONANE Usage And Synthesis
UsesPro-nucleophile and co-catalyst for indium-catalyzed allylations of methyl ethers and carbohydrate derivatives. Catalyst for preparation of linear allenes from other allenes 2 Reactant for: Stereoconvergent Suzuki cross-coupling reactions 3 B-alkyl Suzuki-Miyaura cross-coupling reactions 4 Preparation of borabicyclononanyl amino acid complexes for selective treatment of malignant melanoma 5 Asymmetric synthesis of isomerically pure allenyl boranes through insertion and borotropic rearrangement.
Uses9-Methoxy-9-borabicyclo[3.3.1]nonane is a coupling reagent used in reactions like the synthesis of (-)-brevenal a polycyclic ether.
Uses
  • Pro-nucleophile and co-catalyst for indium-catalyzed allylations of methyl ethers and carbohydrate derivatives
  • Catalyst for preparation of linear allenes from other allenes
Reactant for:
  • Stereoconvergent Suzuki cross-coupling reactions
  • B-alkyl Suzuki-Miyaura cross-coupling reactions
  • Preparation of borabicyclononanyl amino acid complexes for selective treatment of malignant melanoma
  • Asymmetric synthesis of isomerically pure allenyl boranes through insertion and borotropic rearrangement
9-METHOXY-9-BORABICYCLO[3.3.1]NONANE Preparation Products And Raw materials
Preparation Products9-BBN DIMER

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