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METHYL 6-BROMOQUINOLINE-2-CARBOXYLATE

CAS No.
623583-88-0
Chemical Name:
METHYL 6-BROMOQUINOLINE-2-CARBOXYLATE
Synonyms
methyl 2-bromoquinoline-6-carboxylate;METHYL 6-BROMOQUINOLINE-2-CARBOXYLATE;6-Bromo-quinoline-2-carboxylic acid methyl ester;2-Quinolinecarboxylic acid, 6-bromo-, methyl ester
CBNumber:
CB3814044
Molecular Formula:
C11H8BrNO2
Molecular Weight:
266.09
MDL Number:
MFCD08436465
MOL File:
623583-88-0.mol
MSDS File:
SDS
Last updated:2025-07-24 18:13:51

METHYL 6-BROMOQUINOLINE-2-CARBOXYLATE Properties

Boiling point 374.6±22.0 °C(Predicted)
Density 1.557±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
pka 1.18±0.43(Predicted)
Appearance Off-white to pink Solid

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P305+P351+P338

METHYL 6-BROMOQUINOLINE-2-CARBOXYLATE price More Price(8)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
American Custom Chemicals Corporation HCH0356046 METHYL-6-BROMOQUINOLINE-2-CARBOXYLATE 95.00% 623583-88-0 5MG $505.92 2021-12-16 Buy
AK Scientific 4318AJ Methyl6-bromoquinoline-2-carboxylate 623583-88-0 5g $2397 2021-12-16 Buy
Chemenu CM123373 methyl6-bromoquinoline-2-carboxylate 97% 623583-88-0 1g $306 2021-12-16 Buy
Crysdot CD11087141 Methyl6-bromoquinoline-2-carboxylate 97% 623583-88-0 1g $324 2021-12-16 Buy
Chemenu CM123373 methyl6-bromoquinoline-2-carboxylate 97% 623583-88-0 5g $916 2021-12-16 Buy
Product number Packaging Price Buy
HCH0356046 5MG $505.92 Buy
4318AJ 5g $2397 Buy
CM123373 1g $306 Buy
CD11087141 1g $324 Buy
CM123373 5g $916 Buy

METHYL 6-BROMOQUINOLINE-2-CARBOXYLATE Chemical Properties,Uses,Production

Synthesis

Methanol

67-56-1

6-Bromoquinoline-2-carboxylic acid

65148-10-9

METHYL 6-BROMOQUINOLINE-2-CARBOXYLATE

623583-88-0

1c) Synthesis of methyl 6-bromo-2-quinolinecarboxylate A mixture of 6-bromo-2-quinolinecarboxylic acid (331 g, multiple batches, 1.31 mol) and methanesulfonic acid (22 mL, 33 g, 0.34 mol) in methanol (2 L) was refluxed for 6 hours. Upon completion of the reaction, the reaction mixture was neutralized with an aqueous solution of sodium bicarbonate (29 g, 0.34 mol) (350 mL). The resulting suspension was slowly cooled to 20 °C and stirred continuously overnight. The solid product was collected by filtration and the filter cake was washed with water (1 L). The solid product was dried in a vacuum oven at 50 °C for 3 days to give methyl 6-bromo-2-quinolinecarboxylate (294 g, 85% yield). 1H NMR (400 MHz, DMSO-d6) δ 8.52 (d, J = 9 Hz, 1H), 8.40 (d, J = 2 Hz, 1H), 8.14 (d, J = 9 Hz, 1H), 8.08 (d, J = 9 Hz, 1H), 7.97 (m, 1H), 3.93 (s, 3H). ES-LCMS m/z 267 (M + H)+.

References

[1] Patent: US2008/96921, 2008, A1. Location in patent: Page/Page column 32
[2] Tetrahedron, 2014, vol. 70, # 42, p. 7686 - 7690
[3] Patent: WO2011/127643, 2011, A1. Location in patent: Page/Page column 38

67-56-1
65148-10-9
623583-88-0
Synthesis of METHYL 6-BROMOQUINOLINE-2-CARBOXYLATE from Methanol and 6-Bromoquinoline-2-carboxylic acid
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METHYL 6-BROMOQUINOLINE-2-CARBOXYLATE 6-Bromo-quinoline-2-carboxylic acid methyl ester 2-Quinolinecarboxylic acid, 6-bromo-, methyl ester methyl 2-bromoquinoline-6-carboxylate 623583-88-0