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METHYL 6-QUINOLINEACETATE

Product Name
METHYL 6-QUINOLINEACETATE
CAS No.
5622-36-6
Chemical Name
METHYL 6-QUINOLINEACETATE
Synonyms
Methyl 2-(quinolin-6-yl);METHYL 6-QUINOLINEACETATE;methyl quinolin-6-ylacetate;Methyl 2-quinolin-6-ylacetate;Methyl 6-quinolineacetate ,95%;6-Quinolineacetic acid methyl ester;Quinolin-6-Yl-Acetic Acid Methyl Ester
CBNumber
CB0121284
Molecular Formula
C12H11NO2
Formula Weight
201.22
MOL File
5622-36-6.mol
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METHYL 6-QUINOLINEACETATE Property

Boiling point:
196-200 °C(Press: 13 Torr)
Density 
1.186±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
4.82±0.10(Predicted)
Appearance
Light yellow to brown Liquid
CAS DataBase Reference
5622-36-6
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

Precautionary statements

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

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N-Bromosuccinimide Price

TRC
Product number
M320988
Product name
Methyl2-(Quinolin-6-yl)acetate
Packaging
500mg
Price
$105
Updated
2021/12/16
AK Scientific
Product number
X7063
Product name
Methyl6-quinolineacetate
Packaging
10g
Price
$652
Updated
2021/12/16
AK Scientific
Product number
X7063
Product name
Methyl6-quinolineacetate
Packaging
25g
Price
$1226
Updated
2021/12/16
Labseeker
Product number
SC-27553
Product name
Methyl6-Quinolineacetate
Purity
95
Packaging
25g
Price
$1467
Updated
2021/12/16
Ambeed
Product number
A221429
Product name
Methyl2-(quinolin-6-yl)acetate
Purity
98%
Packaging
100mg
Price
$22
Updated
2021/12/16
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METHYL 6-QUINOLINEACETATE Chemical Properties,Usage,Production

Uses

Methyl 2-(Quinolin-6-yl)acetate is a reactuant to prepare triazolopyridazines as tyrosine kinase modulators.

Synthesis

67-56-1

5622-34-4

5622-36-6

Example 1. Preparation of methyl quinoline-6-acetate: Concentrated sulfuric acid (206 mL, 3.868 mol) was slowly added dropwise to a solution of 6-quinolineacetic acid (Compound 1001, 658.2 g, 3.516 mol, Okeanos Tech Co., Catalog No. OK-J-05024) dissolved in 6.5 L of methanol as shown in step i of Scheme 1. A slight exotherm was observed during the dropwise addition. After dropwise addition, the reaction mixture was stirred under reflux conditions for 4 hours. After completion of the reaction, it was cooled to room temperature and the volatile solvent was removed by distillation under reduced pressure. The residue was diluted with 4 L of ethyl acetate and cooled in an ice bath. Subsequently, the pH was adjusted to 4 with 2 N NaOH solution (2.1 L, 1.2 eq.) and then with saturated sodium bicarbonate solution to 8. The organic and aqueous layers were separated and the aqueous layer was extracted twice with ethyl acetate. The combined organic phases were washed sequentially with saturated sodium bicarbonate solution, water and brine, and then dried with anhydrous MgSO4. After filtration, the solvent was evaporated under reduced pressure to give methyl quinoline-6-acetate (compound 1002, 696.8 g, 98% yield) as a clear brown oil: ESMS (M + 1), 202.14; 1H NMR (300.0 MHz, DMSO-d6) δ 8.90 (1H, dd, J = 1.7, 4.2 Hz), 8.14-8.10 (1H , m), 8.08 (1H, d, J = 8.7 Hz), 7.72 (1H, d, J = 1.4 Hz), 7.65 (1H, dd, J = 2.0, 8.7 Hz), 7.40 (1H, dd, J = 4.2, 8.3 Hz), 3.83 (2H, s), 3.73 (3H, s).

References

[1] Patent: WO2010/59668, 2010, A1. Location in patent: Page/Page column 20-21
[2] Patent: WO2016/8011, 2016, A1. Location in patent: Page/Page column 67
[3] Patent: WO2013/19682, 2013, A1. Location in patent: Page/Page column 117
[4] Patent: WO2008/144767, 2008, A1. Location in patent: Page/Page column 110; 115
[5] Journal of Medicinal Chemistry, 2013, vol. 56, # 17, p. 6651 - 6665

METHYL 6-QUINOLINEACETATE Preparation Products And Raw materials

Raw materials

Preparation Products

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METHYL 6-QUINOLINEACETATE Suppliers

Accela ChemBio Inc.
Tel
+1(858) 699-3322
Fax
+1(858) 876-1948
Email
marketing@accelachem.com
Country
United States
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6024
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Alchem Pharmtech,Inc.
Tel
8485655694
Email
sales@alchempharmtech.com
Country
United States
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Aladdin Scientific
Tel
Email
tp@aladdinsci.com
Country
United States
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57505
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Synthonix Inc
Tel
--
Fax
--
Email
info@synthonix.com
Country
United States
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6872
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Aagile Labs Division of Tyger Scientific
Tel
--
Fax
--
Email
tygersci@yahoo.com
Country
United States
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APAC Pharmaceutical, LLC
Tel
--
Fax
--
Email
sales@apacpharma.com
Country
United States
ProdList
6322
Advantage
38

5622-36-6, METHYL 6-QUINOLINEACETATERelated Search:


  • METHYL 6-QUINOLINEACETATE
  • Quinolin-6-Yl-Acetic Acid Methyl Ester
  • Methyl 6-quinolineacetate ,95%
  • Methyl 2-quinolin-6-ylacetate
  • 6-Quinolineacetic acid methyl ester
  • Methyl 2-(quinolin-6-yl)
  • methyl quinolin-6-ylacetate
  • 5622-36-6
  • pharmacetical
  • Heterocycles
  • Acids and Derivatives