716235
2-Bromomethylphenylboronic acid pinacol ester
95%
Synonym(s):
2-(2-(Bromomethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
About This Item
Recommended Products
Quality Level
assay
95%
form
solid
mp
82-86 °C
functional group
bromo
SMILES string
CC1(C)OB(OC1(C)C)c2ccccc2CBr
InChI
1S/C13H18BBrO2/c1-12(2)13(3,4)17-14(16-12)11-8-6-5-7-10(11)9-15/h5-8H,9H2,1-4H3
InChI key
ROIXSNLOYHDYBP-UHFFFAOYSA-N
Related Categories
1 of 4
This Item | 62320 | 1368201 | PHR2561 |
|---|---|---|---|
| assay ≥99% (titration) | assay ≥98.0% (HPLC) | assay - | assay - |
| form powder | form solid | form - | form powder |
| Quality Level 200 | Quality Level 200 | Quality Level - | Quality Level 300 |
| solubility ethanol: soluble 50 mg/mL | solubility water: 0.87 g/L at 22 °C | solubility - | solubility - |
| biological source synthetic | biological source - | biological source - | biological source - |
| description Oxidized form | description - | description - | description Pharmaceutical Secondary Standard; Certified Reference Material |
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk_germany
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
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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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