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464279

Sigma-Aldrich

2-(Trifluoromethoxy)aniline

95%

Synonym(s):

α,α,α-Trifluoro-o-anisidine

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About This Item

Linear Formula:
CF3OC6H4NH2
CAS Number:
1535-75-7
Molecular Weight:
177.12
Beilstein/REAXYS Number:
2803814
EC Number:
216-257-9
MDL number:
MFCD00035959
UNSPSC Code:
12352100
PubChem Substance ID:
24870157
NACRES:
NA.22

Quality Level

200

assay

95%

refractive index

n20/D 1.461 (lit.)

bp

61-63 °C/15 mmHg (lit.)

density

1.301 g/mL at 25 °C (lit.)

SMILES string

Nc1ccccc1OC(F)(F)F

InChI

1S/C7H6F3NO/c8-7(9,10)12-6-4-2-1-3-5(6)11/h1-4H,11H2

InChI key

ZFCOUBUSGHLCDT-UHFFFAOYSA-N

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Application

2-(Trifluoromethoxy)aniline may be used in the preparation of 2-amino-6-(trifluoromethoxy)benzothiazole (SKA-35).

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

129.2 °F - closed cup

flash_point_c

54 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Certificates of Analysis (COA)

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Ananthakrishnan Sankaranarayanan et al.
Molecular pharmacology, 75(2), 281-295 (2008-10-29)
Small-conductance (KCa2.1-2.3) and intermediate-conductance (KCa3.1) calcium-activated K(+) channels are critically involved in modulating calcium-signaling cascades and membrane potential in both excitable and nonexcitable cells. Activators of these channels constitute useful pharmacological tools and potential new drugs for the treatment of

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