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3-AMINO-4-METHYLQUINOLINE

Product Name
3-AMINO-4-METHYLQUINOLINE
CAS No.
50878-90-5
Chemical Name
3-AMINO-4-METHYLQUINOLINE
Synonyms
4-Methylquinolin-3-amine;4-Methyl-3-quinolinamine;3-AMINO-4-METHYLQUINOLINE;3-Quinolinamine, 4-methyl-;4-METHYL-QUINOLIN-3-YLAMINE
CBNumber
CB2836825
Molecular Formula
C10H10N2
Formula Weight
158.2
MOL File
50878-90-5.mol
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3-AMINO-4-METHYLQUINOLINE Property

storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
R262064
Product name
4-METHYL-QUINOLIN-3-YLAMINE
Purity
Aldrich<sup>CPR</sup>
Packaging
1 unit
Price
$30.7
Updated
2025/07/31
Sigma-Aldrich
Product number
R262064
Product name
4-METHYL-QUINOLIN-3-YLAMINE
Purity
AldrichCPR
Packaging
50MG
Price
$29.8
Updated
2024/03/01
AK Scientific
Product number
Y9270
Product name
4-Methylquinolin-3-amine
Packaging
250mg
Price
$253
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
CHM0010252
Product name
3-AMINO-4-METHYLQUINOLINE
Purity
95.00%
Packaging
5MG
Price
$502.39
Updated
2021/12/16
Matrix Scientific
Product number
188747
Product name
4-Methylquinolin-3-amine
Packaging
1g
Price
$660
Updated
2021/12/16
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3-AMINO-4-METHYLQUINOLINE Chemical Properties,Usage,Production

Synthesis

79965-62-1

50878-90-5

4-Methyl-3-nitroquinoline (500 mg, 2.66 mmol) was used as raw material, which was dissolved in concentrated hydrochloric acid (10 mL) and heated to 50 °C. Subsequently, tin(II) chloride dihydrate (1.5 g, 6.6 mmol) was added to the reaction system. The reaction temperature was maintained at 50 °C with continuous stirring overnight. Upon completion of the reaction, the reaction mixture was diluted with water (20 mL) and the pH was adjusted to 9 with 5 N aqueous sodium hydroxide solution. the mixture was cooled to 4 °C and extracted twice with ethyl acetate (30 mL). The organic phases were combined, washed with ice-cold water (40 mL), dried over anhydrous Na2SO4, filtered and concentrated to give 3-amino-4-methylquinoline (340 mg, 80% yield) as a yellow solid. The product was characterized by 1H NMR (400 MHz, CDCl3): δ 8.42 (s, 1H), 7.89-7.91 (m, 1H), 7.79-7.82 (m, 1H), 7.44-7.38 (m, 2H), 3.77 (br s, 2H), 2.37 (s, 3H).

References

[1] Patent: WO2013/14569, 2013, A1. Location in patent: Page/Page column 35
[2] Monatshefte fuer Chemie, 1949, vol. 80, p. 607,615
[3] Journal of the Chemical Society, 1951, p. 2992,2994
[4] Monatshefte fuer Chemie, 1949, vol. 80, p. 607,615
[5] Journal of the Chemical Society, 1953, p. 1915,1918

3-AMINO-4-METHYLQUINOLINE Preparation Products And Raw materials

Raw materials

Preparation Products

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3-AMINO-4-METHYLQUINOLINE Suppliers

A.J Chemicals
Tel
--
Fax
--
Email
sales@ajchem.in
Country
India
ProdList
6100
Advantage
58

50878-90-5, 3-AMINO-4-METHYLQUINOLINERelated Search:


  • 3-AMINO-4-METHYLQUINOLINE
  • 4-Methyl-3-quinolinamine
  • 4-Methylquinolin-3-amine
  • 3-Quinolinamine, 4-methyl-
  • 4-METHYL-QUINOLIN-3-YLAMINE
  • 50878-90-5
  • API intermediates