Ethyl 7-bromoisoquinoline-3-carboxylate
- Product Name
- Ethyl 7-bromoisoquinoline-3-carboxylate
- CAS No.
- 660830-62-6
- Chemical Name
- Ethyl 7-bromoisoquinoline-3-carboxylate
- Synonyms
- Ethyl 7-bromoisoquinoline-3-carboxylate;7-Bromo-isoquinoline-3-carboxylic acid ethyl ester;3-Isoquinolinecarboxylic acid, 7-bromo-, ethyl ester;Ethyl 7-bromoisoquinoline-3-carboxylate ISO 9001：2015 REACH
- CBNumber
- CB42471406
- Molecular Formula
- C12H10BrNO2
- Formula Weight
- 280.12
- MOL File
- 660830-62-6.mol
Ethyl 7-bromoisoquinoline-3-carboxylate Property
- Boiling point:
- 406.4±25.0 °C(Predicted)
- Density
- 1.495±0.06 g/cm3(Predicted)
- storage temp.
- Keep in dark place,Sealed in dry,Room Temperature
- pka
- 2.01±0.33(Predicted)
- Appearance
- Off-white to light yellow Solid
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
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
- 0148AC
- Product name
- Ethyl7-bromoisoquinoline-3-carboxylate
- Packaging
- 250mg
- Price
- $277
- Updated
- 2021/12/16
- Product number
- HCH0369036
- Product name
- ETHYL-7-BROMOISOQUINOLINE-3-CARBOXYLATE
- Purity
- 95.00%
- Packaging
- 5MG
- Price
- $503.99
- Updated
- 2021/12/16
- Product number
- 0148AC
- Product name
- Ethyl7-bromoisoquinoline-3-carboxylate
- Packaging
- 1g
- Price
- $617
- Updated
- 2021/12/16
- Product number
- A375605
- Product name
- Ethyl7-bromoisoquinoline-3-carboxylate
- Purity
- 98%
- Packaging
- 100mg
- Price
- $113
- Updated
- 2021/12/16
- Product number
- A375605
- Product name
- Ethyl7-bromoisoquinoline-3-carboxylate
- Purity
- 98%
- Packaging
- 250mg
- Price
- $185
- Updated
- 2021/12/16
Ethyl 7-bromoisoquinoline-3-carboxylate Chemical Properties,Usage,Production
Synthesis
13209-32-0
13433-00-6
660830-62-6
To a stirred solution of 4-bromophthalaldehyde (1.6 g, 7.74 mmol, 1.0 eq.) in ethanol (20 mL) was added diethyl aminomalonate hydrochloride (1.63 g, 7.74 mmol, 1.0 eq.) and sodium ethanolate (3.9 mL, 11.61 mmol, 1.5 eq.) in turn, and the reaction mixture was stirred at 80 °C under nitrogen protection for 4 for 4 hours. After completion of the reaction, the mixture was cooled to room temperature and the reaction was quenched with saturated ammonium chloride solution. Subsequently, the reaction mixture was extracted with ethyl acetate (2 x 50 mL), the organic phases were combined and dried over anhydrous sodium sulfate. The organic phase was concentrated under reduced pressure to give the crude product. The crude products from the two experiments were combined and purified by fast column chromatography on silica gel, the eluent being a 15-25% ethyl acetate/hexane solvent mixture. The target fractions were collected and concentrated under reduced pressure to afford ethyl 7-bromoisoquinoline-3-carboxylate (1.2 g, 28% yield) as a brown solid. The product was characterized by 1H NMR (400 MHz, CDCl3): δ 1.49 (t, J=7.2Hz, 3H), 4.51-4.57 (m, 2H), 7.86 (s, 2H), 8.24 (s, 1H), 8.56 (s, 1H), 9.28 (s, 1H).
References
[1] Patent: WO2018/15879, 2018, A1. Location in patent: Page/Page column 85
Ethyl 7-bromoisoquinoline-3-carboxylate Preparation Products And Raw materials
Raw materials
Preparation Products
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