641571-11-1

  • Product Name:3-(4-Methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)aniline
  • Molecular Formula:C11H10F3N3
  • Purity:99%
  • Molecular Weight:241.216
Inquiry

Product Details

Reputable Factory Supply Top Purity 3-(4-Methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)aniline 641571-11-1 with Efficient Shipping

  • Molecular Formula:C11H10F3N3
  • Molecular Weight:241.216
  • Vapor Pressure:0mmHg at 25°C 
  • Melting Point:124-126°C 
  • Refractive Index:1.553 
  • Boiling Point:379.805 °C at 760 mmHg 
  • Flash Point:183.5 °C 
  • PSA:43.84000 
  • Density:1.35 g/cm3 
  • LogP:3.36290 

3-(4-Methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)aniline(Cas 641571-11-1) Usage

Chemical Properties

Beige Solid

InChI:InChI=1/C11H10F3N3/c1-7-5-17(6-16-7)10-3-8(11(12,13)14)2-9(15)4-10/h2-6H,15H2,1H3

641571-11-1 Relevant articles

High Turnover Pd/C Catalyst for Nitro Group Reductions in Water. One-Pot Sequences and Syntheses of Pharmaceutical Intermediates

Gallou, Fabrice,Li, Xiaohan,Lipshutz, Bruce H.,Takale, Balaram S.,Thakore, Ruchita R.

supporting information, p. 8114 - 8118 (2021/10/25)

Commercially available Pd/C can be used ...

SYNTHESIS OF 6-METHYL-N1-(4-(PYRIDIN-3-YL)PYRIMIDIN-2-YL)BENZENE-1,3-DIAMINE

-

Page/Page column 40, (2021/04/23)

Processes and useful intermediates for t...

SUBSTITUTED ARYLUREA COMPOUNDS FOR INDUCING APOPTOSIS AND COMPOSITION FOR ANTICANCER COMPRISING THE SAME

-

Paragraph 0141-0145, (2021/08/17)

The present invention relates to a subst...

Method for synthesizing 3-(4-methyl-1H-imidazole-1-yl)-5-(trifluoromethyl) aniline

-

Page/Page column 6-8, (2020/10/14)

The invention relates to a method for sy...

641571-11-1 Process route

3-(4-methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)benzohydrazide

3-(4-methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)benzohydrazide

3-(4-methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)aniline
641571-11-1

3-(4-methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)aniline

Conditions
Conditions Yield
3-(4-methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)benzohydrazide; With sulfuric acid; sodium nitrite; In methanol; at 15 - 25 ℃; for 0.416667h;
In methanol; at 55 - 75 ℃; for 0.416667h; Concentration; Reagent/catalyst; Temperature;
90%
N-(3-amino-5-(trifluoromethyl)phenyl)acetamide
455279-96-6

N-(3-amino-5-(trifluoromethyl)phenyl)acetamide

formaldehyd
50-00-0,30525-89-4,61233-19-0

formaldehyd

2-oxopropanal
78-98-8

2-oxopropanal

3-(4-methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)aniline
641571-11-1

3-(4-methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)aniline

Conditions
Conditions Yield
N-(3-amino-5-(trifluoromethyl)phenyl)acetamide; With ammonium chloride; In ethanol; acetone; at 0 - 20 ℃;
formaldehyd; 2-oxopropanal; In ethanol; water; acetone; at 65 - 70 ℃;
85.4%

641571-11-1 Upstream products

  • 822-36-6
    822-36-6

    4-methyl-1H-imidazole

  • 54962-75-3
    54962-75-3

    [3-bromo-5-(trifluoromethyl)phenyl]amine

  • 916975-92-3
    916975-92-3

    4-methyl-1-(3-nitro-5-(trifluoromethyl)-phenyl)-1H-imidazole

  • 917391-26-5
    917391-26-5

    3-(4-methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)aniline hydrochloride

641571-11-1 Downstream products

  • 895519-92-3
    895519-92-3

    6-methyl-N-{3-(4-methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)phenyl}-5-[4-(pyrid-3-yl)pyrimid-2-yl-amino]nicotinamide

  • 926922-18-1
    926922-18-1

    3-iodo-4-methyl-N-[3-(4-methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)phenyl]benzamide

  • 641571-10-0
    641571-10-0

    nilotinib

  • 1072710-70-3
    1072710-70-3

    6-[[(1,1-dimethylethyl)diphenylsilyl]oxy]-N-[3-(4-methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)phenyl]-1-naphthalenecarboxamide