2-AMINO-5-BROMOBENZONITRILE
- Product Name
- 2-AMINO-5-BROMOBENZONITRILE
- CAS No.
- 39263-32-6
- Chemical Name
- 2-AMINO-5-BROMOBENZONITRILE
- Synonyms
- 4-Bromo-2-cyanoaniline;5-Bromoanthranilonitrile;2-AMINO-5-BROMBENZONITRILE;2-amino-5-bromobenzoltrile;2-AMINO-5-BROMOBENZONITRILE;Benzonitrile, 2-amino-5-bromo-;2-Amino-5-bromobenzonitrile >2-AMINO-5-BROMOBENZONITRILE 97%;2-Amino-5-bromobenzonitrile,97%;2-Amino-5-bromobenzonitrile ,99%
- CBNumber
- CB9453843
- Molecular Formula
- C7H5BrN2
- Formula Weight
- 197.03
- MOL File
- 39263-32-6.mol
2-AMINO-5-BROMOBENZONITRILE Property
- Melting point:
- 96-100 °C(lit.)
- Boiling point:
- 288.4±25.0 °C(Predicted)
- Density
- 1.6480 (rough estimate)
- refractive index
- 1.5500 (estimate)
- storage temp.
- Keep in dark place,Inert atmosphere,Room temperature
- solubility
- Soluble in methanol.
- pka
- 1.11±0.10(Predicted)
- form
- Crystalline Powder
- color
- Off-white to pale brown
- InChI
- InChI=1S/C7H5BrN2/c8-6-1-2-7(10)5(3-6)4-9/h1-3H,10H2
- InChIKey
- OATYCBHROMXWJO-UHFFFAOYSA-N
- SMILES
- C(#N)C1=CC(Br)=CC=C1N
- CAS DataBase Reference
- 39263-32-6(CAS DataBase Reference)
Safety
- Hazard Codes
- Xn,Xi
- Risk Statements
- 20/21/22-43-36/37/38
- Safety Statements
- 36/37-36/37/39-26-22
- RIDADR
- 3439
- WGK Germany
- 3
- Hazard Note
- Irritant
- HazardClass
- 6.1
- PackingGroup
- III
- HS Code
- 29269090
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H301Toxic if swalloed
H302Harmful if swallowed
H312Harmful in contact with skin
H315Causes skin irritation
H317May cause an allergic skin reaction
H319Causes serious eye irritation
H331Toxic if inhaled
H332Harmful if inhaled
H335May cause respiratory irritation
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P264Wash hands thoroughly after handling.
P264Wash skin thouroughly after handling.
P270Do not eat, drink or smoke when using this product.
P280Wear protective gloves/protective clothing/eye protection/face protection.
P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
P405Store locked up.
P501Dispose of contents/container to..…
N-Bromosuccinimide Price
- Product number
- A1960
- Product name
- 2-Amino-5-bromobenzonitrile
- Purity
- >98.0%(GC)
- Packaging
- 1g
- Price
- $37
- Updated
- 2025/07/31
- Product number
- A1960
- Product name
- 2-Amino-5-bromobenzonitrile
- Purity
- >98.0%(GC)
- Packaging
- 5g
- Price
- $102
- Updated
- 2025/07/31
- Product number
- 30454
- Product name
- 2-Amino-5-bromo-benzonitrile
- Packaging
- 500mg
- Price
- $32
- Updated
- 2024/03/01
- Product number
- 30454
- Product name
- 2-Amino-5-bromo-benzonitrile
- Packaging
- 1g
- Price
- $50
- Updated
- 2024/03/01
- Product number
- A602505
- Product name
- 2-Amino-5-bromobenzonitrile
- Packaging
- 5g
- Price
- $60
- Updated
- 2021/12/16
2-AMINO-5-BROMOBENZONITRILE Chemical Properties,Usage,Production
Description
2-Amino-5-bromo-benzonitrile is a heterocyclic building block. It has been used in the synthesis of copper-ligand coordination complexes and 4-amino-3-benzimidazol-2-ylhydroquinolin-2-one-based multi-targeted receptor tyrosine kinase (RTK) inhibitors with anticancer activity.
Chemical Properties
white to light yellow crystal powder
Uses
2-Amino-5-bromobenzonitrile can react with Oxalic acid dimethyl ester to get 5-Bromo-N-methylanthranilonitrile.
Synthesis
1885-29-6
39263-32-6
The general procedure for the synthesis of 2-amino-5-bromobenzonitrile from 2-aminobenzonitrile was as follows: 2-aminobenzonitrile (11.8 g, 0.1 mol) was dissolved in acetic acid (120 ml) and ammonium bromide (10.3 g, 0.105 mol) and hydrogen peroxide (10.2 ml, 35% aqueous solution, 0.105 mol) were added sequentially. The reaction mixture was stirred at room temperature for about 1 hour, followed by continued stirring for 24 hours until LCMS analysis confirmed the completion of the reaction. Upon completion of the reaction, the acetic acid was removed by concentration and the residue was stirred with 30% aqueous sodium hydroxide solution to alkaline. The resulting solid was collected by filtration, washed with water and dried. The dried solid was dissolved in an excess of dichloromethane, the solution was concentrated until a precipitate began to appear and left to crystallize completely. The crystals were collected by filtration and washed with a small amount of dichloromethane to afford the target compound 2-amino-5-bromobenzonitrile as an off-white crystalline solid (19.2 g, 97% yield).1HNMR data: δ 7.61 (1H, d, J=2.5 Hz), 7.43 (1H, dd, J=9,2.5 Hz), 6.75 (1H, d, J=9 Hz), 6.28 ( 2H, br s); LC-MS retention time: 2.24 min.
References
[1] Canadian Journal of Chemistry, 2009, vol. 87, # 2, p. 440 - 447
[2] Patent: WO2007/80401, 2007, A1. Location in patent: Page/Page column 26
[3] Synthetic Communications, 2010, vol. 40, # 6, p. 868 - 876
[4] Synthetic Communications, 2010, vol. 40, # 21, p. 3226 - 3232
[5] Molecular Crystals and Liquid Crystals (1969-1991), 1991, vol. 206, p. 205 - 221
2-AMINO-5-BROMOBENZONITRILE Preparation Products And Raw materials
Raw materials
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View Lastest Price from 2-AMINO-5-BROMOBENZONITRILE manufacturers
- Product
- 2-AMINO-5-BROMOBENZONITRILE 39263-32-6
- Price
- US $1.00/KG
- Min. Order
- 1KG
- Purity
- 99%
- Supply Ability
- 100kg
- Release date
- 2019-07-11