ChemicalBook > CAS DataBase List > ETHYL 6-BROMOQUINOLINE-3-CARBOXYLATE

ETHYL 6-BROMOQUINOLINE-3-CARBOXYLATE

Product Name
ETHYL 6-BROMOQUINOLINE-3-CARBOXYLATE
CAS No.
481054-89-1
Chemical Name
ETHYL 6-BROMOQUINOLINE-3-CARBOXYLATE
Synonyms
ETHYL 6-BROMOQUINOLINE-3-CARBOXYLATE;6-BroMoquinoline-3-carboxylic acid ethyl ester;3-Quinolinecarboxylic acid, 6-bromo-, ethyl ester
CBNumber
CB02465054
Molecular Formula
C12H10BrNO2
Formula Weight
280.12
MOL File
481054-89-1.mol
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ETHYL 6-BROMOQUINOLINE-3-CARBOXYLATE Property

storage temp. 
Sealed in dry,Room Temperature
Appearance
Light yellow to yellow Solid
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H314Causes severe skin burns and eye damage

Precautionary statements

P260Do not breathe dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

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

P301+P330+P331IF SWALLOWED: Rinse mouth. Do NOT induce vomiting.

P303+P361+P353IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower.

P363Wash contaminated clothing before reuse.

P405Store locked up.

P501Dispose of contents/container to..…

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N-Bromosuccinimide Price

TRC
Product number
E900820
Product name
Ethyl6-bromoquinoline-3-carboxylate
Packaging
1g
Price
$415
Updated
2021/12/16
ChemScene
Product number
CS-0061591
Product name
Ethyl6-bromoquinoline-3-carboxylate
Purity
99.12%
Packaging
5g
Price
$448
Updated
2021/12/16
ChemScene
Product number
CS-0061591
Product name
Ethyl6-bromoquinoline-3-carboxylate
Purity
99.12%
Packaging
1g
Price
$112
Updated
2021/12/16
AK Scientific
Product number
3261AQ
Product name
ETHYL6-BROMOQUINOLINE-3-CARBOXYLATE
Packaging
5g
Price
$1146.8
Updated
2021/12/16
ChemScene
Product number
CS-0061591
Product name
Ethyl6-bromoquinoline-3-carboxylate
Purity
99.12%
Packaging
10g
Price
$780
Updated
2021/12/16
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ETHYL 6-BROMOQUINOLINE-3-CARBOXYLATE Chemical Properties,Usage,Production

Synthesis

10601-80-6

20357-20-4

481054-89-1

Step 1: Synthesis of ethyl 6-bromoquinoline-3-carboxylate To a solution of 5-bromo-2-nitrobenzaldehyde (2 g, 9 mmol) in ethanol (46 mL) was sequentially added tin(II) chloride dihydrate (7.95 g, 35.2 mmol) and ethyl 3,3-diethoxypropionate (4.2 mL, 22 mmol). The reaction mixture was heated to 90 °C and maintained for 16 hours. Upon completion of the reaction, it was cooled to room temperature and stirring was continued overnight. Subsequently, the reaction mixture was concentrated and the residue was dissolved in ethyl acetate. The solution was poured into a saturated aqueous sodium bicarbonate solution to form an emulsion. The emulsion was filtered through diatomaceous earth and the diatomaceous earth was rinsed with ethyl acetate. The organic and aqueous layers were separated and the aqueous phase was further extracted with ethyl acetate. All organic phases were combined, washed with brine, dried over magnesium sulfate, filtered and concentrated. Finally, purification by fast column chromatography (eluent: 0-50% ethyl acetate/heptane gradient) gave ethyl 6-bromoquinoline-3-carboxylate (1.41 g, 60% yield) as a solid.

References

[1] Journal of Organic Chemistry, 2010, vol. 75, # 10, p. 3488 - 3491
[2] Patent: US2012/270893, 2012, A1. Location in patent: Page/Page column 32

ETHYL 6-BROMOQUINOLINE-3-CARBOXYLATE Preparation Products And Raw materials

Raw materials

Preparation Products

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ETHYL 6-BROMOQUINOLINE-3-CARBOXYLATE Suppliers

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481054-89-1, ETHYL 6-BROMOQUINOLINE-3-CARBOXYLATERelated Search:


  • 6-BroMoquinoline-3-carboxylic acid ethyl ester
  • ETHYL 6-BROMOQUINOLINE-3-CARBOXYLATE
  • 3-Quinolinecarboxylic acid, 6-bromo-, ethyl ester
  • 481054-89-1