568155
4,4,5,5,-Tetramethyl-2-phenylsulfanylmethyl-1,3,2-dioxaborolane
97%
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
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
10 - Combustible liquids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves
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Articles
The synthesis of biaryl compounds via the Suzuki–Miyaura coupling reaction has become more commonplace now that many arylboronic acids are readily available.
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