Substance
ID:715221
Names and Identifiers
IUPAC Traditional name
3-chloro-4-fluoroaniline
IUPAC name
3-chloro-4-fluoroaniline
Synonyms
3-Chloro-4-fluoroaniline3-氯-4-氟苯胺
Registration numbers
Beilstein Number
MDL Number
EC Number
CAS Number
Properties
Safety Information
TSCA Listed
是
UN Number
UN2811
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), categories 1,2,3
Respiratory sensitization, category 1
Germ cell mutagenicity, categories 1A,1B,2
Carcinogenicity, categories 1A,1B,2
Reproductive toxicity, categories 1A,1B,2
Specific Target Organ Toxicity – Single exposure, categories 1,2
Specific Target Organ Toxicity – Repeated exposure, categories 1,2
Aspiration Hazard, category 1
GHS Precautionary statements
P260-P305+P351+P338-P361-P302+P352-P405-P501A
Safety Statements
26-28-36/37
GHS Hazard statements
H311-H302-H332-H315-H319-H373
European Hazard Symbols
Harmful (X)Risk Statements
20/21/22-33-36/38
Packing Group
III
Hazard Class
6.1
Product Information
Purity
98+%
Physical Property
Density
1.420
Flash Point
149°C(300°F)
Melting Point
44-47°C
Boiling Point
227-230°C
Molecule Details
No Data Available
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Molecular Spectra
No Data Available
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References
• Reaction with triethyl orthoformate, catalyzed by sulfuric acid, to give the N-ethyl-N-formyl derivative (method as Org. Synth. Coll., 4, 420 (1963)), is the first step in a short and efficient strategy for the synthesis of the quinoline antibiotic norfloxacin: J. Chem. Soc., Chem. Commun., 1319 (1995).