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Sodium triacetoxyborohydride_Molecular_structure_CAS_56553-60-7)
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Sodium triacetoxyborohydride

Catalog No. B22060 Name Alfa Aesar
CAS Number 56553-60-7 Website
M. F. C6H9BNaO6 Telephone
M. W. 210.93283 Fax
Purity 95% Email
Storage Chembase ID: 85625

SYNONYMS

Title
三乙酰氧基硼氢化钠
IUPAC name
sodium bis(acetyloxy)boranuidyl acetate
IUPAC Traditional name
sodium bis(acetyloxy)boranuidyl acetate
Synonyms
STAB

DATABASE IDS

CAS Number 56553-60-7
EC Number 000-000-0
Beilstein Number 4047608
MDL Number MFCD00012211

PROPERTIES

Purity 95%
Melting Point ca 110°C dec.
GHS Pictograms GHS02
GHS Pictograms GHS05
GHS Pictograms GHS07
GHS Hazard statements H261-H228-H318-H315-H335
European Hazard Symbols Irritant Irritant (Xi)
European Hazard Symbols Flammable Flammable (F)
GHS Precautionary statements P210-P231+P232-P241-P305+P351+P338-P405-P501A
Risk Statements 11-15-37/38-41
Safety Statements 7/8-26-33-37/39-43-60
Storage Warning Moisture Sensitive
TSCA Listed
Hazard Class 4.3
UN Number UN3396
Packing Group III

DETAILS

REFERENCES

  • Selective reducing agent; review: Org. Prep. Proced. Int., 17, 317 (1985). Reduces aldehydes in the presence of ketones: J. Chem. Soc., Chem. Commun., 535 (1975). For stereoselective reduction of ketones in AcOH, see: Tetrahedron Lett., 273 (1983). Reduces ?-hydroxy ketones diastereoselectively to anti-diols: J. Am. Chem. Soc., 110, 3560 (1988), and cyclic ?-enamino esters selectively to the cis-amino esters: J. Org. Chem., 59, 5328 (1994); Tetrahedron: Asymmetry, 5, 1455 (1994).
  • Excellent reagent for reductive amination of aldehydes and ketones with a wide variety of amines: J. Org. Chem., 61, 3849 (1996); Tetrahedron Lett., 37, 3977 (1996); review: A.C.S. Symp. Ser., 641, 201 (1996).