2-fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyri
CAS : 452972-14-4
Ref. 3D-FF105642
| 1g | Arrêté | ||
| 2g | Arrêté | ||
| 5g | Arrêté | ||
| 10g | Arrêté | ||
| 25g | Arrêté |
Informations sur le produit
Nom :
2-fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyri
Synonymes :
- 2-(2-Fluoro-3-pyridyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
- 2-Fluoro-3-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Pyridine
- 2-Fluoro-3-(tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
- Pyridine, 2-Fluoro-3-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)-
Description :
The cross-coupling reaction is a chemical reaction that involves the coupling of two or more unsaturated molecules. The cross-coupling of boronic acids with organohalides has been extensively studied, and this reaction has become a popular method for the synthesis of complex organic molecules. This type of cross-coupling reaction is usually carried out in an inert atmosphere to prevent oxidation of the product. The experimental optimization algorithm is used to maximize the yield and minimize the time required to produce desired products. The implemented algorithm uses real-time measurement to optimize the parameters, complicating the process by maximizing product yield without compromising on time.
Avis:
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Marque:
Biosynth
Stockage à long terme :
Notes :
Propriétés chimiques
Masse moléculaire :
223.05 g/mol
Formule :
C11H15BFNO2
Degré de pureté :
Min. 95%
InChI :
InChI=1S/C11H15BFNO2/c1-10(2)11(3,4)16-12(15-10)8-6-5-7-14-9(8)13/h5-7H,1-4H3
Code InChI :
InChIKey=YYOZFGQOPNTVGM-UHFFFAOYSA-N
SMILES :
CC1(C)OB(c2cccnc2F)OC1(C)C
MDL:
Point de fusion :
Point d'ébullition :
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Code SH :
