5-Methylquinoline
- Name 5-Methylquinoline
- CAS 7661-55-4
- Purity 99%
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
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3054-95-3
acrylaldehyde diethyl acetal
-
-
108-44-1
1-amino-3-methylbenzene
-
-
612-60-2
7-methylquinoline
-
-
7661-55-4
5-methylquinoline
| Conditions | Yield |
|---|---|
|
With
hydrogenchloride;
In
water;
at 111 ℃;
for 24h;
Overall yield = 16 %;
|
-
-
108-44-1
1-amino-3-methylbenzene
-
-
504-63-2
trimethyleneglycol
-
-
612-60-2
7-methylquinoline
-
-
7661-55-4
5-methylquinoline
| Conditions | Yield |
|---|---|
|
With
tetrachloromethane; iron(III) chloride hexahydrate;
at 150 ℃;
for 8h;
Overall yield = 71 %;
Inert atmosphere;
Sealed tube;
|
7661-55-4 Upstream products
-
116060-10-7
N'-(2,5-Dimethyl-phenyl)-N,N-dimethyl-acetamidine
-
116060-11-8
N'-(2,3-Dimethyl-phenyl)-N,N-dimethyl-acetamidine
-
77515-70-9
5-methyl-2,3,4,6,7,8-hexahydroquinoline
-
23545-77-9
C17 H18 N2
7661-55-4 Downstream products
-
500595-66-4
5-methyl-2-phenylquinoline
-
85656-64-0
5-methyl-8-aminoquinoline
-
85656-77-5
2,4,6-Trimethyl-benzenesulfonate1-amino-8-formylamino-5-methyl-quinolinium;
-
11139-62-1
2-phenyl-quinoline-5-carboxylic acid
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