568155
4,4,5,5,-Tetramethyl-2-phenylsulfanylmethyl-1,3,2-dioxaborolane
97%
Sign Into View Organizational & Contract Pricing
All Photos(1)
About This Item
Recommended Products
Assay
97%
refractive index
n20/D 1.5280 (lit.)
bp
105-108 °C/0.1 mmHg (lit.)
density
1.059 g/mL at 25 °C (lit.)
SMILES string
CC1(C)OB(CSc2ccccc2)OC1(C)C
InChI
1S/C13H19BO2S/c1-12(2)13(3,4)16-14(15-12)10-17-11-8-6-5-7-9-11/h5-9H,10H2,1-4H3
InChI key
DGPGLPBMZOKGON-UHFFFAOYSA-N
Application
4,4,5,5,-Tetramethyl-2-phenylsulfanylmethyl-1,3,2-dioxaborolane is used to prepare aryl/heteroaryl derivatives via the formation of C-C and C-hetero bonds.
It can also be used as:
It can also be used as:
- A starting material in the synthesis of α-aminoboronic acids as serine proteases inhibitors.
- A substrate in the coupling reactions with carbonyl compounds under Ir-catalyzed photoredox conditions.
Storage Class Code
10 - Combustible liquids
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.
A Photoredox Coupling Reaction of Benzylboronic Esters and Carbonyl Compounds in Batch and Flow
Organic Letters, 21(15), 6140-6144 (2019)
Synthesis of boronic acid analogues of α-amino acids by introducing side chains as electrophiles
The Journal of Organic Chemistry, 66(19), 6375-6380 (2001)
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