3-(Trifluoromethyl)aniline

3-(Trifluoromethyl)aniline
Names
	IUPAC name 3-(trifluoromethyl)aniline
	Other names 3-Aminobenzotrifluoride; m-ABTF; m-Trifluoromethylaniline, 3-(Trifluoromethyl)phenyl-1-amine
Identifiers
CAS Number	98-16-8 ;
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL1162293 ;
ChemSpider	7097 ;
ECHA InfoCard	100.002.404
PubChem CID	7375;
UNII	Z1RWM538YN ;
CompTox Dashboard (EPA)	DTXSID9024512 ;
	InChI InChI=1S/C7H6F3N/c8-7(9,10)5-2-1-3-6(11)4-5/h1-4H,11H2 Key: VIUDTWATMPPKEL-UHFFFAOYSA-N ; InChI=1/C7H6F3N/c8-7(9,10)5-2-1-3-6(11)4-5/h1-4H,11H2 Key: VIUDTWATMPPKEL-UHFFFAOYAM;
	SMILES FC(F)(F)c1cc(N)ccc1;
Properties
Chemical formula	C7H6F3N
Molar mass	161.12 g/mol
Density	1.29 g/cm3
Melting point	5 to 6 °C (41 to 43 °F; 278 to 279 K)
Boiling point	187 to 188 °C (369 to 370 °F; 460 to 461 K)
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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	Infobox references

3-(Trifluoromethyl)aniline is a compound with the molecular formula CF₃C₆H₄NH₂. It is an aromatic amine.

Drugs

3-(Trifluoromethyl)aniline is used in the production of:

the herbicide fluometuron.[1] It is synthesized from benzotrifluoride via nitration followed by reduction to meta-H₂NC₆H₄CF₃. 3-(Trifluoromethyl)aniline is then converted to the urea, fluometuron.
Flufenamic acid
Morniflumate
Ufenamate
Flubanilate
Salfluverine
Colfenamate

Siegemund, Günter "Aromatic Compounds with Fluorinated Side-Chains" in Ullmann's Encyclopedia of Industrial Chemistry 2005, Wiley-VCH. doi:10.1002/14356007.a11_349.

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