| Identification | More | [Name]
Bis(hexylene glycolato)diboron | [CAS]
230299-21-5 | [Synonyms]
4,4,4',4',6,6'-HEXAMETHYL-2,2'-BI-1,3,2-DIOXABORINANE
4,4,6-TRIMETHYL-2-(4,4,6-TRIMETHYL-1,3,2-DIOXABORINAN-2-YL)-1,3,2-DIOXABORINANE
BIS(1,3,3-TRIMETHYL-1,3-PROPANEDIOLATO)DIBORON
BIS(2-METHYL-2,4-PENTANEDIOLATO)DIBORON
BIS(HEXYLENE GLYCOLATO)DIBORON
Bis(hexyleneglycolato)diboron,99%
Bis(diisopropyl-L-tartrate glycolato)diboron | [Molecular Formula]
C12H24B2O4 | [MDL Number]
MFCD06246008 | [Molecular Weight]
253.94 | [MOL File]
230299-21-5.mol |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S37/39:Wear suitable gloves and eye/face protection .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . | [WGK Germany ]
3
| [TSCA ]
No | [HazardClass ]
IRRITANT | [HS Code ]
29349990 |
| Hazard Information | Back Directory | [Chemical Properties]
White crystalline powde | [Uses]
Bis(hexylene glycolato)diboron can be used as a reagent:
- To prepare aryl boronate esters via metal-catalyzed direct C-H borylation of aryl compounds.
- In the chemoselective synthesis of C?C coupling products via nickel catalyzed coupling of primary and secondary alkyl halides.
- In the nickel-catalyzed regioselective arylboration of terminal nonactivated alkenes to yield alkyl boranes.
| [Uses]
suzuki reaction |
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