All Photos(1)
About This Item
Empirical Formula (Hill Notation):
C6H13BO2
CAS Number:
Molecular Weight:
127.98
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
≥95%
form
powder
SMILES string
OB(O)C1CCCCC1
InChI
1S/C6H13BO2/c8-7(9)6-4-2-1-3-5-6/h6,8-9H,1-5H2
InChI key
XDRVAZAFNWDVOE-UHFFFAOYSA-N
Related Categories
Application
Reactant involved in:
- HF-free synthesis of tetrabutylammonium trifluoroborates
- Cross-coupling with aromatic amines
- Suzuki cross-coupling reactions
- Arylation and alkylation of diphenylisoxazole
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
Mirei Shou et al.
Chirality, 27(7), 417-421 (2015-05-23)
Three aldohexoses, glucose, galactose, and mannose, and three aldopentoses, arabinose, xylose, and ribose, were derivatized with L-tryptophanamide (L-TrpNH2 ) under alkaline conditions. Using a basic mobile phase (pH 9.2), the three aldohexoses or the three aldopentoses were simultaneously enantioseparated, respectively, but
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service