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3-METHOXY-4-METHYLANILINE


  • CAS
  • Purity
  • 16452-01-0
  • 99%
Inquiry

Chinese factory supply 3-METHOXY-4-METHYLANILINE 16452-01-0 in stock with high standard

  • Molecular Formula: C8H11NO
  • Molecular Weight: 137.181
  • Appearance/Colour: Brown chunky solid 
  • Vapor Pressure: 0.021mmHg at 25°C 
  • Melting Point: 56-60 °C 
  • Refractive Index: 1.549 
  • Boiling Point: 251 °C at 760mmHg 
  • PKA: 4.61±0.10(Predicted) 
  • Flash Point: 109.6 °C 
  • PSA: 35.25000 
  • Density: 1.039 g/cm3 
  • LogP: 2.16700 

3-METHOXY-4-METHYLANILINE(Cas 16452-01-0) Usage

Air & Water Reactions

Sensitive to prolonged exposure to air. Insoluble in water.

Reactivity Profile

3-METHOXY-4-METHYLANILINE neutralizes acids in weakly exothermic reactions to form salts plus water. May be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. May generate hydrogen, a flammable gas, in combination with strong reducing agents such as hydrides. Reacts with oxidizing agents .

Fire Hazard

3-METHOXY-4-METHYLANILINE is probably combustible.

InChI:InChI=1/C8H11NO/c1-6-3-4-7(9)5-8(6)10-2/h3-5H,9H2,1-2H3

16452-01-0 Relevant articles

Preparation method of 6-tert-butyl-3 ', 3', 3-trimethyl pyran [3, 2-a] carbazole

-

Paragraph 0009-0010; 0027-0028, (2020/11/05)

The invention provides a preparation met...

Development of 2-thioxoquinazoline-4-one derivatives as dual and selective inhibitors of dynamin-related protein 1 (Drp1) and puromycin-sensitive aminopeptidase (PSA)

Numadate, Akiyoshi,Mita, Yusuke,Matsumoto, Yotaro,Fujii, Shinya,Hashimoto, Yuichi

, p. 979 - 988 (2015/02/19)

An established inhibitor ot dynamin-rela...

Efficient construction of pyrano [3, 2-a]carbazoles: Application to a biomimetic total synthesis of cyclized monoterpenoid pyrano [3, 2-a]carbazole Alkaloids

Hesse, Ronny,Gruner, Konstanze K.,Kataeva, Olga,Schmidt, Arndt W.,Kn?lker, Hans-Joachim

supporting information, p. 14098 - 14111 (2013/11/06)

We have developed a highly efficient rou...

Iron-mediated total synthesis of 2,7-dioxygenated carbazole alkaloids

Krahl, Micha P.,Kataeva, Olga,Schmidt, Arndt W.,Knoelker, Hans-Joachim

, p. 59 - 64 (2013/02/22)

We describe the efficient iron-mediated ...

16452-01-0 Process route

2-methyl-5-nitroanisole
13120-77-9

2-methyl-5-nitroanisole

ortho-cresidine
16452-01-0

ortho-cresidine

Conditions
Conditions Yield
With iron; acetic acid; at 45 ℃; for 3.5h; Inert atmosphere;
100%
With palladium 10% on activated carbon; hydrogen; In methanol; for 10h; under 3750.38 Torr;
99%
With hydrogen; palladium on activated carbon; In ethanol; water; for 3h; under 2585.81 Torr;
98%
With 5%-palladium/activated carbon; hydrogen; In tetrahydrofuran; for 5h;
98%
With hydrogen; palladium 10% on activated carbon; In ethanol; at 18 - 22 ℃; for 6.5h; under 760.051 Torr;
97%
With palladium 10% on activated carbon; hydrogen; In methanol; at 20 ℃;
97%
With palladium 10% on activated carbon; hydrogen; In methanol; at 20 ℃; for 5.5h; under 750.075 Torr;
95%
With ethanol; nickel; Hydrogenation;
With sodium disulfide;
With hydrogenchloride; ethanol; tin(ll) chloride;
With iron; acetic acid; at 100 ℃; for 2h;
With hydrogen; Ni-Raney; In methanol; at 20 ℃; under 760.051 Torr;
With palladium 10% on activated carbon; hydrogen; In ethyl acetate; for 5h;
With hydrogen; Ni-Raney; In methanol; at 20 ℃; under 760.051 Torr;
With hydrogen; In methanol; at 20 ℃; under 760.051 Torr;
1.86 g
tin(II)chloride dihydrate

tin(II)chloride dihydrate

2-methyl-5-nitroanisole
13120-77-9

2-methyl-5-nitroanisole

ortho-cresidine
16452-01-0

ortho-cresidine

Conditions
Conditions Yield
In ethanol; ethyl acetate;
86%

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