5-Bromonicotinonitrile
5-Bromonicotinonitrile Basic information
- Product Name:
- 5-Bromonicotinonitrile
- Synonyms:
-
- AKOS BBS-00003122
- 3-Bromo-5-cyanopyridine 97%
- 5-Bromo-3-cyanopyridine,97%
- 5-Bromonicotinonitrile,98%
- 3-Cyano-5-broMopyridine
- 5-BroMo-3-pyridinecarbonitrile
- 3-Bromo-5-cyanopyridine, 5-Bromopyridine-3-carbonitrile
- 5-Bromonicotinonitrile 97%
- CAS:
- 35590-37-5
- MF:
- C6H3BrN2
- MW:
- 183.01
- Product Categories:
-
- Boronic Acid
- C6Heterocyclic Building Blocks
- Halogenated Heterocycles
- Heterocyclic Building Blocks
- Pyridine
- Organohalides
- Nucleotides and Nucleosides
- Bases & Related Reagents
- Nucleotides
- blocks
- Bromides
- Carboxes
- Pyridines
- Mol File:
- 35590-37-5.mol
5-Bromonicotinonitrile Chemical Properties
- Melting point:
- 103-107 °C(lit.)
- Boiling point:
- 228.8±20.0 °C(Predicted)
- Density
- 1.72±0.1 g/cm3(Predicted)
- storage temp.
- Inert atmosphere,Room Temperature
- solubility
- Chloroform (Heated), Ethyl Acetate (Slightly), Methanol (Slightly)
- form
- Solid
- pka
- -0.57±0.20(Predicted)
- color
- Pale Yellow to Yellow
- InChI
- InChI=1S/C6H3BrN2/c7-6-1-5(2-8)3-9-4-6/h1,3-4H
- InChIKey
- FTFFHWWIPOQCBC-UHFFFAOYSA-N
- SMILES
- C1=NC=C(Br)C=C1C#N
- CAS DataBase Reference
- 35590-37-5(CAS DataBase Reference)
Safety Information
- Hazard Codes
- Xi,Xn
- Risk Statements
- 36/37/38-20/21/22
- Safety Statements
- 26-36-36/37/39
- RIDADR
- 3276
- WGK Germany
- 3
- Hazard Note
- Irritant
- HazardClass
- 6.1
- PackingGroup
- III
- HS Code
- 29333990
MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ALFA
5-Bromonicotinonitrile Usage And Synthesis
Chemical Properties
White crystalline powder
Synthesis
625-92-3
35590-37-5
General procedure for the synthesis of 3-cyano-5-bromopyridine from 3,5-dibromopyridine: iPrMgCl (2M in THF, 4.1 mL) and THF (5 mL) were added to a flask containing dry LiCl (0.35 g, 8.24 mmol) at 15 °C. After stirring for 15 min, a solution of 3-bromo-1-benzylnitrile (1.46 g, 8.03 mmol) in THF (1 mL) was slowly added to the reaction mixture and stirring was continued for 15 min. Subsequently, DMF (1.3 mL, 12 mmol) was added dropwise at 0 °C and the mixture was stirred for 2 hours. Upon completion of the reaction, aqueous NH3 (7 mL, 28-30%) and I2 (4.06 g, 16 mmol) were added to the mixture. After stirring for 2 h at room temperature, the reaction mixture was poured into saturated aqueous Na2SO3 solution and extracted with CHCl3 (3 x 30 mL). The organic layers were combined, dried with Na2SO4 and filtered. After removing the solvent under reduced pressure, the residue was purified by silica gel short column chromatography (eluent: hexane/ethyl acetate = 9:1, v/v) to afford pure 3-cyano-5-bromopyridine (0.73 g) in 71% yield. Most of the nitrile compounds involved in this study were commercially available and were identified by comparison with real samples.
References
[1] Tetrahedron, 2013, vol. 69, # 5, p. 1462 - 1469
5-BromonicotinonitrileSupplier
- Tel
- 15369111890
- sjzqiyuekeji@163.com
- Tel
- 18210857532; 18210857532
- jkinfo@jkchemical.com
- Tel
- 4006356688 18621169109
- market03@meryer.com
- Tel
- 821-50328103-801 18930552037
- 3bsc@sina.com
- Tel
- 400-6106006
- saleschina@alfa-asia.com
5-Bromonicotinonitrile(35590-37-5)Related Product Information
- 3-Cyanopyridine
- 3-Hydroxypyridine
- 2-Chloro-3-cyanopyridine
- 3-Bromo-5-methylpyridine
- ETHYL 2-CYANOACRYLATE
- 4-Cyanopyridine
- DBDCB
- 1-Hexadecylpyridinium bromide
- 3-Aminopyridine
- Chlorfenapyr
- 3-Bromoanisole
- methyl 3-bromopicolinate
- 3-BROMO-5-NITROPYRIDINE
- 3-Bromo-5-iodo-pyridine
- 3-BROMO-4-FLUOROPYRIDINE
- 3-Bromo-5-chloropyridine
- 3-BROMOPYRIDINE-2-CARBOXYLIC ACID
- 3-Bromo-5-hydroxypyridine