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1-(4-chlorobutyl)-4-fluorobenzene

  • CAS No.: 54540-58-8
  • Purity: 99%
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1-(4-chlorobutyl)-4-fluorobenzene GMP Manufacturer Global Trade 54540-58-8 with Fast Delivery

  • Molecular Formula: C10H12ClF
  • Molecular Weight: 186.657
  • Vapor Pressure: 0.0291mmHg at 25°C 
  • Refractive Index: 1.495 
  • Boiling Point: 253.5 °C at 760 mmHg 
  • Flash Point: 120.2 °C 
  • PSA: 0.00000 
  • Density: 1.092 g/cm3 
  • LogP: 3.38720 

1-(4-chlorobutyl)-4-fluorobenzene(Cas 54540-58-8) Usage

General Description

1-(4-Chlorobutyl)-4-fluorobenzene is a complex organic chemical compound with the molecular formula C10H13ClF. This chemical compound consists of an aromatic benzene ring that is attached to a fluorine atom at the forth carbon position and a four-carbon aliphatic side chain at the first carbon position, and this chain substitute contains a chlorine atom. Due to the presence of reactive chloro- and fluoro- groups, it is likely used as an intermediate compound in the synthesis of other chemical substances in various chemical industries. Detailed information about its physical properties, uses, safety measures, and toxicity has not been well-documented and may vary depending on its purity and the specific conditions under which it is handled or processed.

InChI:InChI=1/C10H12ClF/c11-8-2-1-3-9-4-6-10(12)7-5-9/h4-7H,1-3,8H2

54540-58-8 Relevant articles

Structure-Kinetic Profiling of Haloperidol Analogues at the Human Dopamine D2 Receptor

Fyfe, Tim J.,Kellam, Barrie,Sykes, David A.,Capuano, Ben,Scammells, Peter J.,Lane, J. Robert,Charlton, Steven J.,Mistry, Shailesh N.

, p. 9488 - 9520 (2019/11/11)

Haloperidol is a typical antipsychotic d...

Structure-activity relationship studies of SYA 013, a homopiperazine analog of haloperidol

Peprah, Kwakye,Zhu, Xue Y.,Eyunni, Suresh V.K.,Etukala, Jagan R.,Setola, Vincent,Roth, Bryan L.,Ablordeppey, Seth Y.

scheme or table, p. 1671 - 1678 (2012/04/10)

Structure-activity relationship studies ...

Functional group tolerant Kumada-Corriu-Tamao coupling of nonactivated alkyl halides with aryl and heteroaryl nucleophiles: Catalysis by a nickel pincer complex permits the coupling of functionalized Grignard reagents

Vechorkin, Oleg,Proust, Valerie,Hu, Xile

supporting information; experimental part, p. 9756 - 9766 (2011/03/19)

A nickel(II) pincer complex [(MeNN2)NiCl...

Indole derivatives as 5-HT1A and/or 5-HT2 ligands

-

, (2008/06/13)

Pharmacologically active indole derivati...

54540-58-8 Process route

C<sub>18</sub>H<sub>16</sub>ClFO<sub>4</sub>
84648-52-2

C18 H16 ClFO4

1-(4-chlorobutyl)-4-fluorobenzene
54540-58-8

1-(4-chlorobutyl)-4-fluorobenzene

1-(but-3-en-1-yl)-4-fluorobenzene
2248-13-7

1-(but-3-en-1-yl)-4-fluorobenzene

C<sub>16</sub>H<sub>16</sub>ClF
84648-61-3

C16 H16 ClF

3-Chloro-benzoic acid 4-(4-fluoro-phenyl)-butyl ester
84648-56-6

3-Chloro-benzoic acid 4-(4-fluoro-phenyl)-butyl ester

1,3-Dichlorobenzene
541-73-1

1,3-Dichlorobenzene

Conditions
Conditions Yield
In various solvent(s); at 100 ℃; Mechanism; CIDNP, thermolyse;
4-chlorobutyl bromide
6940-78-9

4-chlorobutyl bromide

4-flourophenylmagnesium bromide
352-13-6

4-flourophenylmagnesium bromide

1-(4-chlorobutyl)-4-fluorobenzene
54540-58-8

1-(4-chlorobutyl)-4-fluorobenzene

Conditions
Conditions Yield
With N,N,N,N,-tetramethylethylenediamine; [((Me)NN2)NiCl]; In tetrahydrofuran; at 20 ℃; for 2h; Inert atmosphere;
76%

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    C18 H16 ClFO4

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    4-chlorobutyl bromide

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