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5-Methylquinoline

  • Name 5-Methylquinoline
  • CAS 7661-55-4
  • Purity 99%
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Product Details

Manufacturer supply 5-Methylquinoline 7661-55-4 with sufficient stock and high standard

  • Molecular Formula: C10H9 N
  • Molecular Weight: 143.188
  • Vapor Pressure: 0.0175mmHg at 25°C 
  • Melting Point: 19°C 
  • Refractive Index: 1.6219 
  • Boiling Point: 262.7°Cat760mmHg 
  • PKA: 5.2(at 20℃) 
  • Flash Point: 104.4°C 
  • PSA: 12.89000 
  • Density: 1.076g/cm3 
  • LogP: 2.54320 

5-Methylquinoline(Cas 7661-55-4) Usage

General Description

5-Methylquinoline, also known as 5-methyl-1-azanaphthalene, is a heterocyclic aromatic compound with the chemical formula C10H9N. It is a derivative of quinoline and is commonly used as a building block in the synthesis of pharmaceuticals, agrochemicals, and dyes. 5-Methylquinoline is a yellowish liquid with a distinct odor, and it is mainly produced through the Friedl?nder synthesis or through the methylation of quinoline. It is used in the production of antimalarial drugs, as well as in the synthesis of dyes and pigments. Additionally, 5-Methylquinoline has been studied for its potential use in the treatment of various diseases, including cancer and neurodegenerative disorders. However, it is important to handle 5-Methylquinoline with care as it is toxic and can cause skin and eye irritation when in contact.

InChI:InChI=1/C10H9N/c1-8-4-2-6-10-9(8)5-3-7-11-10/h2-7H,1H3

7661-55-4 Relevant articles

Transition metal eight-coordination. IV. Tetrakis(5,7-disubstituted-8-quinolinolato)tungsten(V) salts

Archer, Ronald D.,Bonds Jr., Wesley D.,Pribush, Robert A.

, p. 1550 - 1555 (1972)

Violet, paramagnetic [WQ4]+ ions have be...

Using Data Science To Guide Aryl Bromide Substrate Scope Analysis in a Ni/Photoredox-Catalyzed Cross-Coupling with Acetals as Alcohol-Derived Radical Sources

Doyle, Abigail G.,Gandhi, Shivaani S.,Jiang, Shutian,Kariofillis, Stavros K.,Martinez Alvarado, Jesus I.,?urański, Andrzej M.

supporting information, p. 1045 - 1055 (2022/01/19)

Ni/photoredox catalysis has emerged as a...

Catalytic Aerobic Dehydrogenatin of N-Heterocycles by N-Hydoxyphthalimide

Chen, Weidong,Tang, Hao,Wang, Weilin,Fu, Qiang,Luo, Junfei

supporting information, p. 3905 - 3911 (2020/08/10)

Catalytic methods for the aerobic dehydr...

Method for preparation of quinoline compounds

-

Paragraph 0046-0048, (2020/11/12)

The invention discloses a green preparat...

A methylation platform of unconventional inert aryl electrophiles: Trimethylboroxine as a universal methylating reagent

Feng, Boya,Yang, Yudong,You, Jingsong

, p. 6031 - 6035 (2020/07/10)

Methylation is one of the most fundament...

7661-55-4 Process route

acrylaldehyde diethyl acetal
3054-95-3

acrylaldehyde diethyl acetal

1-amino-3-methylbenzene
108-44-1

1-amino-3-methylbenzene

7-methylquinoline
612-60-2

7-methylquinoline

5-methylquinoline
7661-55-4

5-methylquinoline

Conditions
Conditions Yield
With hydrogenchloride; In water; at 111 ℃; for 24h; Overall yield = 16 %;
1-amino-3-methylbenzene
108-44-1

1-amino-3-methylbenzene

trimethyleneglycol
504-63-2

trimethyleneglycol

7-methylquinoline
612-60-2

7-methylquinoline

5-methylquinoline
7661-55-4

5-methylquinoline

Conditions
Conditions Yield
With tetrachloromethane; iron(III) chloride hexahydrate; at 150 ℃; for 8h; Overall yield = 71 %; Inert atmosphere; Sealed tube;

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