9-Borabicyclo[3.3.1]nonane - 0.5 M in THF , CAS No.280-64-8

CAS: 280-64-8 Cat. No.: B130058 Molecular Weight: 122.02 Beilstein Registry Number: 605509 EC Number: 206-000-9 PubChem CID: 6327450
AVAILABLE TO ORDER
GRADE & PURITY 0.5 M in THF
Synonyms
AKOS015833689 | 9-borabicyclo [3.3,1 ]nonane | 9-borabicyclo[3, 3,1]nonane | EINECS 206-000-9 | DTXSID10167572 | FT-0657566 | Q-101083 | 1,1-diallyl-2-oxohydrazine | 9-Borabicyclo(3.3.1)nonane | 1H-Indole-3-acetic acid, 1-benzoyl-2-methyl- | 9-BBN
Storage
Room temperature,Argon charged
Shipped In
Normal
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Size
Status
Price
Qty
100ml
B130058-100ml
≥10
$28.90
500ml
B130058-500ml
3
$99.90
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Why this grade

0.5 M in THF for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature,Argon charged Ships Normal Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Differentiation of symmetrical diols by reduction of the corresponding cyclic acetals with 9-BBN.
Selective hydroboration reduction reagent.
Protecting group for alkenes
Reactant for: 
• Linear SPPS synthesis of ubiquitin derivatives
• Copper-catalyzed cross-coupling reactions of organoboron compounds with primary alkyl halides and pseudohalides
• Intramolecular insertion of alkenes into palladium-nitrogen bonds
• Preparation of (phosphonoacetyl)ornithine to study effect on arginine biosynthetic genes in yeast
• Hetero-Diels-Alder reaction for synthesis of spirocyclic alkaloids

9-Borabicyclo[3.3.1]nonane is an organic compound, which is generally used as a hydroborating agent. It is thermally stable, less sensitive to oxygen and water when compared to other dialkyl boranes. It is commonly used to prepare aldehydes from alkynes.



application:

9-BBN monomer acts as a selective hydroboration reagent in synthetic organic chemistry. It is employed in Suzuki reactions as well as in the preparation of terminal alcohols by the region selective addition of alkenes followed by oxidative cleavage using hydrogen peroxide. It is also used in copper-catalyzed cross-coupling reactions of organoboron compounds with primary alkyl halides and pseudohalides. It acts as a protecting group for alkenes. Further, it is used as a reactant for Hetero-Diels-Alder reaction for the synthesis of spirocyclic alkaloids. In addition to this, it is used in intramolecular insertion of alkenes into palladium-nitrogen bonds.

Specifications

Synonyms
AKOS015833689 | 9-borabicyclo [3.3, 1 ]nonane | 9-borabicyclo[3, 3, 1]nonane | EINECS 206-000-9 | DTXSID10167572 | FT-0657566 | Q-101083 | 1, 1-diallyl-2-oxohydrazine | 9-Borabicyclo(3.3.1)nonane | 1H-Indole-3-acetic acid, 1-benzoyl-2-methyl- | 9-BBN
Specifications & Purity
0.5 M in THF
Storage
Room temperature, Argon charged
Shipped In
Normal
Names and Identifiers
Pubchem Sid504764050
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504764050
Canonical Smiles[B]1C2CCCC1CCC2
InChIKeyAMKGKYQBASDDJB-UHFFFAOYSA-N
INCHI1S/C8H14B/c1-3-7-5-2-6-8(4-1)9-7/h7-8H,1-6H2
Isomeric SMILES [B]1C2CCCC1CCC2
WGK Germany 3
PubChem CID 6327450
Molecular Weight 122.02
Beilstein 605509

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

3D Structure
Interactive Chemical Structure Model





Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

12 results found

Lot NumberCertificate TypeDateItem
G2201335Certificate of AnalysisApr 03, 2026 B130058
G2201336Certificate of AnalysisApr 03, 2026 B130058
D2615625Certificate of AnalysisMar 11, 2026 B130058
D2615626Certificate of AnalysisMar 11, 2026 B130058
D2615627Certificate of AnalysisMar 11, 2026 B130058
D2509312Certificate of AnalysisApr 01, 2025 B130058
D2509313Certificate of AnalysisApr 01, 2025 B130058
H2527197Certificate of AnalysisApr 01, 2025 B130058
H2527198Certificate of AnalysisApr 01, 2025 B130058
H2527199Certificate of AnalysisApr 01, 2025 B130058
E2416024Certificate of AnalysisMay 28, 2022 B130058
G2201337Certificate of AnalysisMay 28, 2022 B130058

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Chemical and Physical Properties
SolubilityMiscible with ether, hexane, benzene, toluene, carbon tetrachloride, chloroform, dimethylsulfide and dichloromethane. Slightly miscible with cyclohexane, dimethoxyethane, diglyme and dioxane.
SensitivityAir & Moisture Sensitive
Flash Point(°F)-2°F
Flash Point(°C)-19℃
Molecular Weight121.010 g/mol
XLogP3
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count0
Rotatable Bond Count0
Exact Mass121.119 Da
Monoisotopic Mass121.119 Da
Topological Polar Surface Area0.000 Ų
Heavy Atom Count9
Formal Charge0
Complexity80.700
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Documents & Articles
Citations of This Product
References
1. Kun Zhang, Xiaoni Wang, Minggang Tian, Zhiming Gou, Yujing Zuo.  (2021)  The diversity of the coordination bond generated a POSS-based fluorescent probe for the reversible detection of Cu(II), Fe(III) and amino acids.  Journal of Materials Chemistry B,  (47): (9744-9753).  [PMID:34787631] [10.1039/D1TB01947C]
2. HuaQing Liang, QiHua Zhou, YongJiang Long, WanChu Wei, Shuo Feng, GuoDong Liang, FangMing Zhu.  (2018)  Synthesis and self-assembly of a novel amphiphilic diblock copolymer consisting of isotactic polystyrene and 1,4-trans-polybutadiene-graft-poly(ethylene oxide).  RSC Advances,  (23): (12752-12759).  [PMID:35541237] [10.1039/C8RA01288A]
Solution Calculators
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