| Identification | More | [Name]
BORANE-N,N-DIETHYLANILINE COMPLEX | [CAS]
13289-97-9 | [Synonyms]
BORANE-N,N-DIETHYLANILINE
BORANE-N,N-DIETHYLANILINE COMPLEX
N,N-DIETHYLANILINE BORANE
n,n-diethylanilineborane,deanb
n-diethylbenzenamine)trihydro-((beta-4)-boro
(N,N-diethylaniline)trihydroboron | [EINECS(EC#)]
236-305-2 | [Molecular Formula]
C10H18BN | [MDL Number]
MFCD00013187 | [Molecular Weight]
163.07 | [MOL File]
13289-97-9.mol |
| Safety Data | Back Directory | [Risk Statements ]
R10:Flammable.
R14:Reacts violently with water. | [Safety Statements ]
S16:Keep away from sources of ignition-No smoking .
S33:Take precautionary measures against static discharges .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
S43:In case of fire, use ... (indicate in the space the precise type of fire-fighting equipment. If water increases the risk add-Never use water) . | [RIDADR ]
UN 3398 4.3/PG 2
| [WGK Germany ]
3
| [HazardClass ]
3.1 | [PackingGroup ]
II | [HS Code ]
29299090 |
| Hazard Information | Back Directory | [Chemical Properties]
clear colorless to amber liquid | [Uses]
Reactant for:
- Diastereoselective reduction of prochiral enone intermediates
- Borylation of aryl halides
- Reductions of ketones, acids, esters, amides, and nitriles
- Investigations of borane source on enantioselectivity in enantiopure oxazaborolidine-catalyzed asymmetric borane reduction of ketones
Reactant for synthesis of:
- Chromanol derivatives as CETP inhibitors for the treatment of cardiovascular disease
- Allylic alcohols via enantioselective reductions
- Pinacolboranes for one-pot synthesis of unsymmetrical biaryls
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