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3-Methoxyquinoline

Product Name
3-Methoxyquinoline
CAS No.
6931-17-5
Chemical Name
3-Methoxyquinoline
Synonyms
3-Methoxyquinoline;Quinoline, 3-methoxy-;3-Methoxyquinoline ISO 9001:2015 REACH
CBNumber
CB92222551
Molecular Formula
C10H9NO
Formula Weight
159.18
MOL File
6931-17-5.mol
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3-Methoxyquinoline Property

storage temp. 
Sealed in dry,Room Temperature
Appearance
Colorless to light yellow Liquid
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Safety

HS Code 
2933499090
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

TRC
Product number
M219375
Product name
3-Methoxyquinoline
Packaging
10mg
Price
$45
Updated
2021/12/16
AK Scientific
Product number
W7911
Product name
3-Methoxyquinoline
Packaging
1g
Price
$123
Updated
2021/12/16
AK Scientific
Product number
W7911
Product name
3-Methoxyquinoline
Packaging
5g
Price
$305
Updated
2021/12/16
Matrix Scientific
Product number
074647
Product name
3-Methoxyquinoline
Purity
95+%
Packaging
1g
Price
$225
Updated
2021/12/16
Matrix Scientific
Product number
074647
Product name
3-Methoxyquinoline
Purity
95+%
Packaging
5g
Price
$695
Updated
2021/12/16
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3-Methoxyquinoline Chemical Properties,Usage,Production

Synthesis

5332-24-1

124-41-4

6931-17-5

Step 1: Under nitrogen protection, 3-bromoquinoline (6.5 mL, 48 mmol) was dissolved in anhydrous dimethylformamide (80 mL), followed by the addition of 30% sodium methanol solution (16 mL, 54 mmol) and copper iodide (458 mg, 2.4 mmol). The reaction mixture was heated to reflux with continuous stirring for 16 hours. After completion of the reaction, the mixture was cooled to room temperature and hydrolyzed by adding water. The reaction mixture was extracted with ether (Et2O) and the organic layer was separated. The organic layer was washed sequentially with water and saturated brine and dried over anhydrous magnesium sulfate. After filtration, the organic phase was concentrated under reduced pressure to give 3-methoxyquinoline as a colorless oil in 94% yield. The product was confirmed by 1H NMR (300 MHz, CDCl3) and mass spectrometry (APCI, pos. 30V): 1H NMR δ 8.45 (d, 1H, J=2.9 Hz), 7.85 (dd, 1H, J=8.1, 1.2 Hz), 7.49 (dd, 1H, J=8.1, 1.2 Hz), 7.36-7.25 (m, 2H) , 7.12 (d, 1H, J=2.9 Hz), 3.67 (s, 3H); MS m/z: [M+H]+ 160.

References

[1] European Journal of Medicinal Chemistry, 2017, vol. 127, p. 621 - 631
[2] Tetrahedron, 2002, vol. 58, # 6, p. 1125 - 1129

3-Methoxyquinoline Preparation Products And Raw materials

Raw materials

Preparation Products

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3-Methoxyquinoline Suppliers

Shanghai Longsheng chemical Co.,Ltd.
Tel
021-58099652-8005 13585536065
Fax
021-58099609
Email
bin.wu@shlschem.com
Country
China
ProdList
9883
Advantage
59
Shanghai Hanhong Scientific Co.,Ltd.
Tel
021-54306202 13764082696
Email
info@hanhongsci.com
Country
China
ProdList
42934
Advantage
64
China DongFan Chemical Co.,LTD
Tel
86-0571-85151182
Fax
86-0571-85151182
Country
China
ProdList
5691
Advantage
66
Shandong Xiya Chemical Co., Ltd
Tel
4009903999 13355009207
Fax
0539-6365991
Email
3007715519@qq.com
Country
China
ProdList
18729
Advantage
57
Chengdu Forest Science and Technology Development Co., Ltd.
Tel
18030648795
Fax
028-61777050
Email
sales@cdforestchem.com
Country
China
ProdList
1998
Advantage
58
Shanghai Topbiochem Technology Co., Ltd
Tel
+86-21-60341587
Fax
+86-21-61294319
Email
sales@topbiochem.com
Country
China
ProdList
6175
Advantage
58
SynAsst Chemical.
Tel
021-60343070
Fax
021-35122006
Country
China
ProdList
12740
Advantage
55
Runpharm Technology Limited
Tel
18171398856 2968382473
Fax
0086-21-50758330
Email
service@runpharm.com
Country
China
ProdList
716
Advantage
55
HBCChem, Inc.
Tel
+1-510-219-6317
Fax
+1-650-486-1361
Email
sales@hbcchem.com
Country
United States
ProdList
10648
Advantage
60
Bide Pharmatech Ltd.
Tel
400-164-7117 13681763483
Fax
+86-21-61629029
Email
product02@bidepharm.com
Country
China
ProdList
39966
Advantage
60
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View Lastest Price from 3-Methoxyquinoline manufacturers

Career Henan Chemical Co
Product
3-Methoxyquinoline 6931-17-5
Price
US $1.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
KG/T
Release date
2019-12-20