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73624-47-2

73624-47-2 Structure

73624-47-2 Structure
IdentificationBack Directory
[Name]

B-ISOPINOCAMPHEYL-9-BORABICYCLO[3.3.1]NONANE
[CAS]

73624-47-2
[Synonyms]

R-ALPINE-BORANE
R-ALPINE-BORANE(R)
R-Alpine-Borane®
R-ALPINE-BORANE 97%
r-alpine-borane tm solution
R-Alpine-Borane(R) solution
R-ALPINE-BORANE 0.5 M in THF
R-Alpine-Borane? solution
R-alpine-borane (0.5M soln. in thf)
R-Alpine-Borane(R) solution 0.5 M in THF
B-ISOPINOCAMPHEYL-9-BORABICYCLO[3.3.1]NONANE
(R)-B-isopinocampheyl-9-borabicyclo[3.3.1]nonane
R-2,7,7-trimethylnorpinanborabicyclo(3.3.1)nonane
b-isopinocampheyl-9-borabicyclo[3.3.1]nonane solution
9-Borabicyclo[3.3.1]nonane, 9-(2,6,6-trimethylbicyclo[3.1.1]hept-3-yl)-
9-(2,6,6-Trimethylbicyclo[3.1.1]Heptan-3-yl)-9-borabicyclo[3.3.1]Nonane
R-Alpine-Borane solution,B-Isopinocampheyl-9-borabicyclo[3.3.1]nonane solution
9-[(1R,3R,4S,5R)-4,6,6-trimethyl-3-bicyclo[3.1.1]heptanyl]-9-borabicyclo[3.3.1]nonane
R-Alpine-Borane? (R)-2,6,6-trimethyl-4-(9-borabicyclo[3.3.1]nonan-9-yl)bicyclo[3.1.1]heptane
[Molecular Formula]

C18H31B
[MDL Number]

MFCD00074776
[MOL File]

73624-47-2.mol
[Molecular Weight]

258.25
Chemical PropertiesBack Directory
[alpha ]

-3 º (NEAT)
[Boiling point ]

>55 °C(lit.)
[density ]

0.896 g/mL at 25 °C
[Fp ]

1 °F
[optical activity]

[α]21/D -22°, c = 12 in THF
Safety DataBack Directory
[Hazard Codes ]

F,Xn
[Risk Statements ]

11-19-22-36/37/38-17-40-36/37
[Safety Statements ]

16-26-27-36/37/39-24-6-36/37
[RIDADR ]

UN 1993 3/PG 2
[WGK Germany ]

3
[HazardClass ]

4.3
[PackingGroup ]

III
Hazard InformationBack Directory
[Uses]

R-Alpine-Borane? solution may be used to prepare:
  • (R)-5-(Benzyloxy)pent-3-y-2-ol, an intermediate for the stereoselective total synthesis of (-)-stagonolide D.
  • (R)-1-(p-Tolyl)-1-pentyn-3-ol, an intermediate for the enatioselective synthesis of (R)-incrustoporin.
  • N-(tert-Butyloxycarbonyl)-(4S)-[4-2H]-1-L-homoserine tert-butyl ester, an intermediate for synthesizing (4S)-[4-2H]-L-homoserine.
[General Description]

R-Alpine-Borane? is a chiral reducing agent, synthesized from (+)-α-pinene via hydroboration.
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