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2-Methoxy-5-(trifluoromethyl)aniline

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2-Methoxy-5-(trifluoromethyl)aniline Basic information

Product Name:
2-Methoxy-5-(trifluoromethyl)aniline
Synonyms:
  • BUTTPARK 50\01-75
  • 3-AMINO-4-METHOXYBENZOTRIFLUORIDE
  • 6-METHOXY-ALFA,ALFA,ALFA-TRIFLUORO-M-TOLUIDINE
  • 6-METHOXY-ALPHA,ALPHA,ALPHA-TRIFLUORO-M-TOLUIDINE
  • 2-AMINO-4-TRIFLUOROMETHYLANISOLE
  • 2-METHOXY-5-(TRIFLUOROMETHYL)ANILINE
  • 2-METHOXY-5-TRIFLUOROMETHYL-PHENYLAMINE
  • 2-METHOXY-5-(TRIFLUOROMETHYL)ANILINE, 96 %
CAS:
349-65-5
MF:
C8H8F3NO
MW:
191.15
EINECS:
626-005-3
Product Categories:
  • Anilines, Aromatic Amines and Nitro Compounds
  • Miscellaneous
Mol File:
349-65-5.mol
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2-Methoxy-5-(trifluoromethyl)aniline Chemical Properties

Melting point:
58-60 °C (lit.)
Boiling point:
230.1±40.0 °C(Predicted)
Density 
1.2645 (estimate)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
pka
3.31±0.10(Predicted)
form 
Crystalline Powder
color 
Beige-gray to brown
BRN 
2835713
InChI
InChI=1S/C8H8F3NO/c1-13-7-3-2-5(4-6(7)12)8(9,10)11/h2-4H,12H2,1H3
InChIKey
RKUSRLUGUVDNKP-UHFFFAOYSA-N
SMILES
C1(N)=CC(C(F)(F)F)=CC=C1OC
CAS DataBase Reference
349-65-5(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xn,Xi
Risk Statements 
20/21/22-36/37/38
Safety Statements 
26-36-36/37/39
RIDADR 
UN2811
WGK Germany 
3
Hazard Note 
Irritant
HazardClass 
6.1
PackingGroup 
III
HS Code 
29222990

MSDS

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2-Methoxy-5-(trifluoromethyl)aniline Usage And Synthesis

Chemical Properties

Beige-greyish to brownish crystalline powder

Uses

2-Methoxy-5-(trifluoromethyl)aniline may be used in chemical synthesis.

Definition

ChEBI: 2-Methoxy-5-(trifluoromethyl)aniline is a member of (trifluoromethyl)benzenes.

Synthesis

394-25-2

349-65-5

Example 51 General procedure for the synthesis of 4-(8-methoxy-5-(trifluoromethyl)quinazolin-2-ylamino)phenyl)(morpholino)methanone (Compound 500) PP028218.0002: Step 1. Prepare a mixture of 2-methoxy-5-(trifluoromethyl)aniline A. A methanolic solution of 4-methoxy-3-nitrobenzotrifluoride and 10% Pd/C catalyst (10% loading) was stirred overnight at room temperature in a hydrogen atmosphere. Upon completion of the reaction, the mixture was filtered through a diatomaceous earth pad to remove the catalyst, and the filtrate was concentrated under reduced pressure and dried under vacuum to afford the target product 2-methoxy-5-(trifluoromethyl)aniline A in 99% yield as an off-white solid.ESI-MS m/z: 192.1 (MH+).

References

[1] Synthesis, 2006, # 19, p. 3316 - 3340
[2] Patent: WO2007/117607, 2007, A2. Location in patent: Page/Page column 363-364
[3] Journal of the American Chemical Society, 1952, vol. 74, p. 3011,3012
[4] Zhurnal Prikladnoi Khimii (Sankt-Peterburg, Russian Federation), 1955, vol. 28, p. 969,972
[5] Chem.Abstr., 1956, p. 4880

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