ChemicalBook > CAS DataBase List > 7-Bromo-3-chloroquinoline

7-Bromo-3-chloroquinoline

Product Name
7-Bromo-3-chloroquinoline
CAS No.
1246549-62-1
Chemical Name
7-Bromo-3-chloroquinoline
Synonyms
7-Bromo-3-chloroquinoline;Quinoline, 7-bromo-3-chloro-
CBNumber
CB92538861
Molecular Formula
C9H5BrClN
Formula Weight
242.5
MOL File
1246549-62-1.mol
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7-Bromo-3-chloroquinoline Property

Boiling point:
314.5±22.0 °C(Predicted)
Density 
1.673±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
0.99±0.25(Predicted)
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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

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P321Specific treatment (see … on this label).

P332+P313IF SKIN irritation occurs: Get medical advice/attention.

P362Take off contaminated clothing and wash before reuse.

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N-Bromosuccinimide Price

TRC
Product number
B416715
Product name
7-Bromo-3-chloroquinoline
Packaging
10mg
Price
$45
Updated
2021/12/16
AK Scientific
Product number
4689AA
Product name
7-Bromo-3-chloroquinoline
Packaging
250mg
Price
$255
Updated
2021/12/16
Matrix Scientific
Product number
119850
Product name
7-Bromo-3-chloroquinoline
Purity
95+%
Packaging
250mg
Price
$468
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
HCH0368234
Product name
7-BROMO-3-CHLOROQUINOLINE
Purity
95.00%
Packaging
5MG
Price
$503.35
Updated
2021/12/16
Matrix Scientific
Product number
119850
Product name
7-Bromo-3-chloroquinoline
Purity
95+%
Packaging
1g
Price
$1170
Updated
2021/12/16
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7-Bromo-3-chloroquinoline Chemical Properties,Usage,Production

Synthesis

59278-65-8

621-62-5

1246549-62-1

General procedure for the synthesis of 7-bromo-3-chloroquinoline from 2-amino-4-bromobenzaldehyde and chloroacetaldehyde diethyl acetal: 2-chloro-1,1-diethoxyethane (4.50 mL, 30.0 mmol), 2-amino-4-bromobenzaldehyde (3.00 g, 15.0 mmol), and p-toluenesulfonic acid monohydrate (0.285 g, 1.500 mmol) were dissolved in toluene (50 mL), assembled with a Dean-Stark manifold, and heated to reflux at 110 °C for 3 hours. Upon completion of the reaction, the solvent was evaporated under reduced pressure and the residue was dissolved in ethyl acetate and washed with saturated aqueous sodium bicarbonate. The aqueous layer was then extracted with ethyl acetate, the organic phases were combined, dried over anhydrous sodium sulfate and concentrated to dryness. The crude product was purified by silica gel column chromatography with 20-50% dichloromethane/hexane as eluent to give the title compound 7-bromo-3-chloroquinoline (1.97 g, 8.12 mmol, 54% yield) as a yellow solid. Mass spectrum (ESI+) m/e 241.8/243.8 [M+H]+; 1H NMR (400 MHz, DMSO-d6) δ 7.85 (dd, J = 8.84, 2.02 Hz, 1H), 7.98 (d, J = 8.59 Hz, 1H), 8.29 (d, J = 1.77 Hz, 1H), 8.65 (d, J = 2.02 Hz, 1H), 8.94 (d, J = 2.53 Hz, 1H).

References

[1] Patent: WO2014/108858, 2014, A1. Location in patent: Page/Page column 37, 38

7-Bromo-3-chloroquinoline Preparation Products And Raw materials

Raw materials

Preparation Products

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7-Bromo-3-chloroquinoline Suppliers

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