2-CHLOROQUINAZOLIN-4-AMINE
- Product Name
- 2-CHLOROQUINAZOLIN-4-AMINE
- CAS No.
- 59870-43-8
- Chemical Name
- 2-CHLOROQUINAZOLIN-4-AMINE
- Synonyms
- Nsc75185;IFLAB-BB F2108-0111;2-CHLOROQUINAZOLIN-4-AMINE;2-chloro-4-Quinazolinamine;4-Amino-2-chloroquinazoline;4-Quinazolinamine,2-chloro-;2-Chloro-4-aminoquinazoline;2-Chloroquinazolin-4-ylamine
- CBNumber
- CB7329616
- Molecular Formula
- C8H6ClN3
- Formula Weight
- 179.61
- MOL File
- 59870-43-8.mol
2-CHLOROQUINAZOLIN-4-AMINE Property
- storage temp.
- 2-8°C(protect from light)
- Appearance
- White to off-white Solid
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- C895655
- Product name
- 2-Chloroquinazolin-4-amine
- Packaging
- 50mg
- Price
- $130
- Updated
- 2021/12/16
- Product number
- C895655
- Product name
- 2-Chloroquinazolin-4-amine
- Packaging
- 100mg
- Price
- $200
- Updated
- 2021/12/16
- Product number
- 8921AB
- Product name
- 2-Chloroquinazolin-4-amine
- Packaging
- 100mg
- Price
- $103
- Updated
- 2021/12/16
- Product number
- 8921AB
- Product name
- 2-Chloroquinazolin-4-amine
- Packaging
- 250mg
- Price
- $130
- Updated
- 2021/12/16
- Product number
- HCH0142857
- Product name
- 2-CHLOROQUINAZOLIN-4-AMINE
- Purity
- 98.00%
- Packaging
- 5MG
- Price
- $500.7
- Updated
- 2021/12/16
2-CHLOROQUINAZOLIN-4-AMINE Chemical Properties,Usage,Production
Synthesis
607-68-1
59870-43-8
General procedure for the synthesis of 2-chloroquinazolin-4-amine using 2,4-dichloroquinazoline as starting material: 2,4-dichloroquinazoline (2.0 g, 10 mmol) was dissolved in tetrahydrofuran (THF, 10 mL), followed by addition of ammonia (28-30%, 18 mL). The reaction mixture was stirred at room temperature overnight. After completion of the reaction, the reaction mixture was diluted with ethyl acetate (EtOAc) and washed sequentially with saturated sodium bicarbonate (NaHCO3) solution, water and brine. The organic phase was dried with anhydrous sodium sulfate (Na2SO4), filtered and concentrated under reduced pressure. The resulting crude product was washed with ethyl acetate (EtOAc) to afford 2-chloroquinazolin-4-amine (1.3 g, 72% yield) as a white solid. The structure of the product was confirmed by 1H NMR (400 MHz, DMSO-d6): δ 7.52-7.48 (m, 1H), 7.6-7.58 (m, 1H), 7.8-7.76 (m, 1H), 8.22-8.20 (m, 1H), 8.32 (bs, 2H).
References
[1] Bioorganic and Medicinal Chemistry Letters, 2000, vol. 10, # 11, p. 1175 - 1179
[2] Bioorganic and Medicinal Chemistry Letters, 2005, vol. 15, # 10, p. 2565 - 2569
[3] Patent: US2008/306053, 2008, A1. Location in patent: Page/Page column 65
[4] Journal of the American Chemical Society, 1948, vol. 70, p. 4264
[5] Journal of Medicinal Chemistry, 2008, vol. 51, # 24, p. 7855 - 7865
2-CHLOROQUINAZOLIN-4-AMINE Preparation Products And Raw materials
Raw materials
Preparation Products
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