387-45-1

  • Product Name:2-Chloro-6-fluorobenzaldehyde
  • Molecular Formula:C7H4ClFO
  • Purity:99%
  • Molecular Weight:158.56
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Product Details;

CasNo: 387-45-1

Molecular Formula: C7H4ClFO

Appearance: white to yellow solid

Top Purity Buy High Quality 2-Chloro-6-fluorobenzaldehyde 387-45-1 Efficient Shipping

  • Molecular Formula:C7H4ClFO
  • Molecular Weight:158.56
  • Appearance/Colour:white to yellow solid 
  • Vapor Pressure:0.272mmHg at 25°C 
  • Melting Point:32-35 °C(lit.) 
  • Refractive Index:1.559 
  • Boiling Point:203.8 °C at 760 mmHg 
  • Flash Point:77.1 °C 
  • PSA:17.07000 
  • Density:1.352 g/cm3 
  • LogP:2.29160 

2-Chloro-6-fluorobenzaldehyde(Cas 387-45-1) Usage

Chemical Properties

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Uses

2-Chloro-6-fluorobenzaldehyde was used in the synthesis of novel copolymers of methyl 2-cyano-3-dihalophenyl-2-propenoates and styrene.

General Description

2-Chloro-6-fluorobenzaldehyde undergoes piperidine catalyzed Knoevenagel condensation reaction with methyl cyanoacetate to yield methyl 2-cyano-3-dihalophenyl-2-propenoate.

Consumer Uses

ECHA has no public registered data indicating whether or in which chemical products the substance might be used. ECHA has no public registered data on the routes by which this substance is most likely to be released to the environment.

InChI:InChI=1/C7H4ClFO/c8-6-2-1-3-7(9)5(6)4-10/h1-4H

387-45-1 Relevant articles

Latent Nucleophilic Carbenes

Marchenko, Anatoliy,Koidan, Georgyi,Hurieva, Anastasiya,Shvydenko, Kostiantyn,Rozhenko, Alexander B.,Rusanov, Eduard B.,Kyrylchuk, Andrii A.,Kostyuk, Aleksandr

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Using DFT and ab initio calculations, we...

Monodentate Transient Directing Group Enabled Pd-Catalyzed Ortho-C-H Methoxylation and Chlorination of Benzaldehydes

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387-45-1 Process route

(2-chloro-6-fluorophenyl)methanol
56456-50-9

(2-chloro-6-fluorophenyl)methanol

2-chloro-6-fluorobenzaldehyde
387-45-1

2-chloro-6-fluorobenzaldehyde

Conditions
Conditions Yield
With 4-methyl-morpholine; chromium(VI) oxide; hydrogenchloride; In diethyl ether; chloroform; at 65 ℃; for 0.1h; microwave irradiation;
98%
With 1-methyl-1H-imidazole; [2,2]bipyridinyl; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; tetrakis(acetonitrile)copper(I)tetrafluoroborate; In acetonitrile; at 20 ℃;
98%
With dmap; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; copper diacetate; In neat (no solvent); at 80 ℃; for 18h; Green chemistry;
95%
With 1-methyl-1H-imidazole; [2,2]bipyridinyl; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; tetrakis(acetonitrile)copper(I) trifluoromethanesulfonate; In acetonitrile; at 20 - 50 ℃; for 2.5h; chemoselective reaction; Sealed tube;
94%
With 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; sodium carbonate; N-Phenylglycine; copper(ll) bromide; In water; for 8h; Reflux; Schlenk technique;
91%
With dipotassium peroxodisulfate; at 55 ℃; for 0.25h; Ionic liquid;
87%
With tert.-butylhydroperoxide; tetrabutylammomium bromide; In decane; benzene; at 40 ℃; for 24h; chemoselective reaction; Inert atmosphere; Sealed tube;
75%
N-[(2-chloro-6-fluorophenyl)methylidene]hydroxylamine
443-33-4

N-[(2-chloro-6-fluorophenyl)methylidene]hydroxylamine

2-chloro-6-fluorobenzaldehyde
387-45-1

2-chloro-6-fluorobenzaldehyde

Conditions
Conditions Yield
With iron(III) chloride; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; oxygen; In water; toluene; at 60 ℃; for 5h; under 760.051 Torr;
87%

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387-45-1 Downstream products

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    3-chlorofluorobenzene

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