222674
3-Fluoro-2-methylaniline
99%
Synonym(s):
3-Fluoro-o-toluidine
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About This Item
Linear Formula:
FC6H3(CH3)NH2
CAS Number:
Molecular Weight:
125.14
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
99%
form
liquid
refractive index
n20/D 1.542 (lit.)
bp
89-91 °C/15 mmHg (lit.)
mp
7 °C (lit.)
density
1.099 g/mL at 25 °C (lit.)
functional group
fluoro
SMILES string
Cc1c(N)cccc1F
InChI
1S/C7H8FN/c1-5-6(8)3-2-4-7(5)9/h2-4H,9H2,1H3
InChI key
SLDLVGFPFFLYBM-UHFFFAOYSA-N
Application
3-Fluoro-2-methylaniline was used in the synthesis of 2-amino-1,7,9-trimethylimidazo[4,5-g]quinoxaline.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
186.8 °F - closed cup
Flash Point(C)
86 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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I Achiwa et al.
Chemical & pharmaceutical bulletin, 42(2), 408-409 (1994-02-01)
A new mutagen, 2-amino-1,7,9-trimethylimidazo[4,5-g]quinoxaline (1), isolated from beef extract, was synthesized from 3-fluoro-2-methylaniline via an intermediate, 2,8-dimethyl-7-methylaminoquinoxaline (7a). Its 2-methylanalog (2) was also synthesized from the same intermediate. The synthetic 1 showed the same mutagenic activity as the isolated mutagen.
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