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9-Borabicyclo[3.3.1]nonane solution_Molecular_structure_CAS_280-64-8)
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9-Borabicyclo[3.3.1]nonane solution

Catalog No. 151076 Name Sigma Aldrich
CAS Number 280-64-8 Website http://www.sigmaaldrich.com
M. F. C8H15B Telephone 1-800-521-8956
M. W. 122.0157 Fax
Purity Email
Storage Chembase ID: 140672

SYNONYMS

Title
9-硼双环[3.3.1]壬烷 溶液
IUPAC name
(1s,5s)-9-borabicyclo[3.3.1]nonane
IUPAC Traditional name
(1s,5s)-9-borabicyclo[3.3.1]nonane
Synonyms
9-BBN

DATABASE IDS

CAS Number 280-64-8
PubChem SID 24849089
Beilstein Number 605509
MDL Number MFCD00074742

PROPERTIES

Concentration 0.5 M in THF
Empirical Formula (Hill Notation) C8H15B
Density 0.894 g/mL at 25 °C
Flash Point -17 °C
Flash Point 1.4 °F
GHS Pictograms GHS02
GHS Pictograms GHS07
GHS Signal Word Danger
GHS Hazard statements H225-H260-H319-H335
European Hazard Symbols Flammable Flammable (F)
European Hazard Symbols Irritant Irritant (Xi)
MSDS Link Download
GHS Precautionary statements P210-P223-P231 + P232-P261-P370 + P378-P422
RID/ADR UN 3399 4.3/PG 1
Risk Statements 11-14/15-19-36/37
Safety Statements 16-26-43
Supplemental Hazard Statements May form explosive peroxides.
Hazard Class 4.3
UN Number 3399
Packing Group 1
German water hazard class 3

DETAILS

Description (English)
Application
Differentiation of symmetrical diols by reduction of the corresponding cyclic acetals with 9-BBN.6
Selective hydroboration reduction reagent.
Protecting group for alkenes†Reactant for:
• Linear SPPS synthesis of ubiquitin derivatives1
• Copper-catalyzed cross-coupling reactions of organoboron compounds with primary alkyl halides and pseudohalides2
• Intramolecular insertion of alkenes into palladium-nitrogen bonds3
• Preparation of (phosphonoacetyl)ornithine to study effect on arginine biosynthetic genes in yeast4
• Hetero-Diels-Alder reaction for synthesis of spirocyclic alkaloids5
Packaging
4×25, 100, 800 mL in Sure/Seal™
8, 18 L in Kilo-Lab™
View returnable container options.
Description (简体中文)
Application
使用 9-BBN 对相应环状缩醛进行还原以鉴别对称二醇。6
选择性硼氢化还原试剂。
Protecting group for alkenes†Reactant for:
• Linear SPPS synthesis of ubiquitin derivatives1
• Copper-catalyzed cross-coupling reactions of organoboron compounds with primary alkyl halides and pseudohalides2
• Intramolecular insertion of alkenes into palladium-nitrogen bonds3
• Preparation of (phosphonoacetyl)ornithine to study effect on arginine biosynthetic genes in yeast4
• Hetero-Diels-Alder reaction for synthesis of spirocyclic alkaloids5
包装
4×25, 100, 800 mL in Sure/Seal™
8, 18 L in Kilo-Lab™
View returnable container options.

REFERENCES