Methyl 5-bromonicotinate
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Methyl 5-bromonicotinate ??
- ???
- 96-100 °C
- ?? ?
- 241.7±20.0 °C(Predicted)
- ??
- 1.579±0.06 g/cm3(Predicted)
- ?? ??
- Inert atmosphere,Room Temperature
- ???
- ?????(?? ???), ???(?? ???)
- ??? ??
- ??
- ??? ??
- ??? ??
- ?? ?? (pKa)
- 0.84±0.20(Predicted)
- ??
- ???
- ???
- ?? ?? ?????.
- InChI
- InChI=1S/C7H6BrNO2/c1-11-7(10)5-2-6(8)4-9-3-5/h2-4H,1H3
- InChIKey
- AAJZXPWBILCHAW-UHFFFAOYSA-N
- SMILES
- C1=NC=C(Br)C=C1C(OC)=O
- CAS ??????
- 29681-44-5(CAS DataBase Reference)
??
- ?? ? ?? ??
- ?? ? ???? ?? (GHS)
| ??? ?? | Xi | ||
|---|---|---|---|
| ?? ???? ?? | 37/38-41-36/37/38 | ||
| ????? | 26-39-37/39 | ||
| WGK ?? | 3 | ||
| ?? ?? | IRRITANT | ||
| HS ?? | 29333990 | ||
| ???? ??? | 11 - Combustible Solids | ||
| Hazard Classifications | Eye Dam. 1 Skin Irrit. 2 STOT SE 3 |
Methyl 5-bromonicotinate C??? ??, ??, ??
??? ??
white powder??
A substrate used in a microwave-assisted, palladium-catalyzed arylation of acetone as its TMS enol ether.?? ??
Methyl 5-bromonicotinate could be used to synthesize Pyridine alkaloids from Rubiaceae with various organometallic reagents by palladium-catalyzed cross-coupling reactions. This compound is a derivative of 5-bromonicotinic acid (BrnicH) which has been widely used in the last decade to obtain MOF materials with unique luminescence, magnetism, catalysis, and adsorption through assembling with lanthanide ions and transition metal ions, such as Cu(II), Co(II), Cd(II), Zn(II), and Pb(II)[1-2].Methyl 5-bromonicotinate ?? ?? ? ???
???
?? ??
2-(5-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)pyridin-3-yl)propan-2-ol
3-BroMo-5-(???-1-?-2-?)???
METHYL 5-METHYLNICOTINATE
5-Bromo-3-pyridinemethanol
Methyl 5-aminopyridine-3-carboxylate
??5-(4-(????????)??)???-3-???????
??5-(3-(????????)??)???-3-???????
??5-(???-4-?)???-3-??????
5-Bromonicotinic acid
Methyl 5-bromonicotinate ?? ??
???( 353)?? ??
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