Home Cart Sign in  
Chemical Structure| 613-19-4 Chemical Structure| 613-19-4
Chemical Structure| 613-19-4

2-Methylquinolin-3-ol

CAS No.: 613-19-4

4.5 *For Research Use Only !

Cat. No.: A914373 Purity: 95%

Change View

Size Price

US Stock

Global Stock

In Stock
100mg łÍͶÊÊ Inquiry Inquiry
250mg łÿ§¶ÊÊ Inquiry Inquiry
1g łÇ§î¶ÊÊ Inquiry Inquiry

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • 100mg

    łÍͶÊÊ

  • 250mg

    łÿ§¶ÊÊ

  • 1g

    łÇ§î¶ÊÊ

In Stock

- +

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of [ 613-19-4 ]

CAS No. :613-19-4
Formula : C10H9NO
M.W : 159.18
SMILES Code : OC1=CC2=CC=CC=C2N=C1C
MDL No. :MFCD02239638
InChI Key :OMQWBTOTNRMKAK-UHFFFAOYSA-N
Pubchem ID :594394

Safety of [ 613-19-4 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501

Application In Synthesis of [ 613-19-4 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 613-19-4 ]

[ 613-19-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 613-19-4 ]
  • [ 120121-01-9 ]
  • 3-(1-(3-chlorophenyl)ethoxy)-2-methylquinoline [ No CAS ]
YieldReaction ConditionsOperation in experiment
76% With triphenylphosphine; In tetrahydrofuran; at 20℃; for 18h; In a 30 mL eggplant type flask,2-methylquinolin-3-ol (160 mg, 1.0 mmol),1-Chloroethylbenzene (140 mg, 1.0 mmol),And a suspension of cesium carbonate (320 mg, 1.0 mmol) in dimethylformamide (DMF, 3 mL) was heated and stirred at 70 C. for 5 hours.The reaction solution was extracted with ethyl acetate, washed three times with water,Dried over magnesium sulfate, filtered and concentrated.The obtained residue was purified by silica gel column chromatography,The compound of the present invention (Compound No. 1-1) (200 mg) as an objective compound was obtained in a yield of 76%.
 

Historical Records

Technical Information

Categories

Related Functional Groups of
[ 613-19-4 ]

Alcohols

Chemical Structure| 666735-19-9

A327285 [666735-19-9]

2-Methyl-1,6-naphthyridin-3-ol

Similarity: 0.95

Chemical Structure| 826-81-3

A106027 [826-81-3]

2-Methyl-8-quinolinol

Similarity: 0.93

Chemical Structure| 354573-94-7

A970327 [354573-94-7]

2-Methyl-1H-indol-7-ol

Similarity: 0.88

Chemical Structure| 1121-25-1

A229033 [1121-25-1]

2-Methylpyridin-3-ol

Similarity: 0.88

Chemical Structure| 613-21-8

A382079 [613-21-8]

6-Hydroxy-2-methylquinoline

Similarity: 0.88

Related Parent Nucleus of
[ 613-19-4 ]

Quinolines

Chemical Structure| 826-81-3

A106027 [826-81-3]

2-Methyl-8-quinolinol

Similarity: 0.93

Chemical Structure| 84689-36-1

A754114 [84689-36-1]

3-Methoxy-2-methylquinoline

Similarity: 0.89

Chemical Structure| 613-21-8

A382079 [613-21-8]

6-Hydroxy-2-methylquinoline

Similarity: 0.88

Chemical Structure| 60131-25-1

A158795 [60131-25-1]

6-Bromo-2-methylquinolin-3-ol

Similarity: 0.87

Chemical Structure| 92855-35-1

A846088 [92855-35-1]

2-Methyl-3-phenoxyquinoline

Similarity: 0.87