2-Chloro-6-fluorobenzaldehyde
2-Chloro-6-fluorobenzaldehyde
  • CAS No.:387-45-1
Other grades of this product :
2-Chloro-6-fluorobenzaldehyde Basic information
Product Name:2-Chloro-6-fluorobenzaldehyde
Synonyms:2-Choro-6-Fluoro Benzaldehyde;2-Chloro-6-fluorobenzaldehyde,min.96%;2-CHLORO-6-FLUOROBENZALDEHYDE,99%;2-Chloro-6-fluorobenzaldehyde97%;2-Chlor-6-fluorbenzaldehyd;4-Chloro-6-fluorobenzaldehyde;2-Chloro-6 Florobenzaldehyde;2-fluoro-6-chlorobenzene Methylal
CAS:387-45-1
MF:C7H4ClFO
MW:158.56
EINECS:206-860-5
Product Categories:Aldehydes;C7;Carbonyl Compounds;Aryl Fluorinated Building Blocks;Building Blocks;Carbonyl Compounds;FINE Chemical & INTERMEDIATES;Aromatic Aldehydes & Derivatives (substituted);Aromatics;Intermediates;Chemical Synthesis;Fluorinated Building Blocks;Organic Building Blocks;Organic Fluorinated Building Blocks;Benzaldehyde;Fluorobenzene;Other Fluorinated Organic Building Blocks;Fluorine series
Mol File:387-45-1.mol
2-Chloro-6-fluorobenzaldehyde Chemical Properties
Melting point 32-35 °C(lit.)
Boiling point 92 °C (10 mmHg)
density 1.3310 (estimate)
Fp 215 °F
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility Chloroform (Slightly), Ethyl Acetate (Slightly)
form Crystalline Solid
color White to yellow
Water Solubility Insoluble
Sensitive Air Sensitive
BRN 2245530
CAS DataBase Reference387-45-1(CAS DataBase Reference)
EPA Substance Registry SystemBenzaldehyde, 2-chloro-6-fluoro- (387-45-1)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-37/39-36
WGK Germany 1
TSCA T
HazardClass IRRITANT
HS Code 29130000
MSDS Information
ProviderLanguage
2-Chloro-6-fluorobenzaldehyde English
ACROS English
SigmaAldrich English
ALFA English
2-Chloro-6-fluorobenzaldehyde Usage And Synthesis
Chemical Propertieswhitetoyellowcrystallinesoli
Uses2-Chloro-6-fluorobenzaldehyde was used in the synthesis of novel copolymers of methyl 2-cyano-3-dihalophenyl-2-propenoates and styrene.
General Description2-Chloro-6-fluorobenzaldehyde undergoes piperidine catalyzed Knoevenagel condensation reaction with methyl cyanoacetate to yield methyl 2-cyano-3-dihalophenyl-2-propenoate.

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