89634-75-3

  • Product Name2-CHLORO-5-FLUOROBENZOTRIFLUORIDE
  • Molecular FormulaC7H3ClF4
  • Molecular Weight198.547
  • Purity99%
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Quick Details

  • CasNo: 89634-75-3
  • Molecular Formula: C7H3ClF4
  • Purity: 99%

Trustworthy Factory Supply Top Purity 99% 2-CHLORO-5-FLUOROBENZOTRIFLUORIDE 89634-75-3 with Safe Delivery

  • Molecular Formula:C7H3ClF4
  • Molecular Weight:198.547
  • Boiling Point:152.1±35.0℃ (760 Torr) 
  • Flash Point:50.8±19.4℃ 
  • PSA:0.00000 
  • Density:1.427±0.06 g/cm3 (20 oC 760 Torr) 
  • LogP:3.49790 

89634-75-3 Relevant articles

A Novel, Base-induced Fragmentation of Hantzsch-type 4-Aryl-1,4-dihydropyridines

McInally, Thomas,Tinker, Alan C.

, p. 1837 - 1844 (2007/10/02)

Hantzsch-type 1,4-dihydropyridine deriva...

Antihypertensive 2-phenyl Hantzsch dihydropyridines

-

, (2008/06/13)

There are described compounds of formula...

89634-75-3 Process route

2-(2-bromoethyl)isoindoline-1,3-dione
574-98-1

2-(2-bromoethyl)isoindoline-1,3-dione

3-methyl 5-(1-methylethyl) 4-(3-chloro-6-fluoro-2-(trifluoromethyl)phenyl)-2-(fluoromethyl)-1,4-dihydro-6-methyl-3,5-pyridinedicarboxylate
95445-79-7

3-methyl 5-(1-methylethyl) 4-(3-chloro-6-fluoro-2-(trifluoromethyl)phenyl)-2-(fluoromethyl)-1,4-dihydro-6-methyl-3,5-pyridinedicarboxylate

N-vinylphthalimide
3485-84-5,26809-43-8

N-vinylphthalimide

1-chloro-4-fluoro-2-(trifluoromethyl)benzene
89634-75-3

1-chloro-4-fluoro-2-(trifluoromethyl)benzene

3-methyl 5-(1-methylethyl) 2-(fluoromethyl)-6-methylpyridine-3,5-dicarboxylate
117751-90-3

3-methyl 5-(1-methylethyl) 2-(fluoromethyl)-6-methylpyridine-3,5-dicarboxylate

3-methyl 5-(1-methylethyl) 2-<fluoro-(2,3,5,9b-tetrahydro-5-oxo-oxazolo<2,3-a>isoindol-9b-yl)methyl>-6-methylpyridine-3,5-dicarboxylate
117752-00-8,117752-02-0

3-methyl 5-(1-methylethyl) 2-isoindol-9b-yl)methyl>-6-methylpyridine-3,5-dicarboxylate

Conditions
Conditions Yield
With sodium hydride; Yield given. Multistep reaction. Further byproducts given; 1.) DMF, 0 deg C, 2.) DMF, 20 deg C, 3 h;
61%
48%
53%
2-(2-bromoethyl)isoindoline-1,3-dione
574-98-1

2-(2-bromoethyl)isoindoline-1,3-dione

3-methyl 5-(1-methylethyl) 4-(3-chloro-6-fluoro-2-(trifluoromethyl)phenyl)-2-(fluoromethyl)-1,4-dihydro-6-methyl-3,5-pyridinedicarboxylate
95445-79-7

3-methyl 5-(1-methylethyl) 4-(3-chloro-6-fluoro-2-(trifluoromethyl)phenyl)-2-(fluoromethyl)-1,4-dihydro-6-methyl-3,5-pyridinedicarboxylate

N-vinylphthalimide
3485-84-5,26809-43-8

N-vinylphthalimide

1-chloro-4-fluoro-2-(trifluoromethyl)benzene
89634-75-3

1-chloro-4-fluoro-2-(trifluoromethyl)benzene

3-methyl 5-(1-methylethyl) 2-(fluoromethyl)-6-methylpyridine-3,5-dicarboxylate
117751-90-3

3-methyl 5-(1-methylethyl) 2-(fluoromethyl)-6-methylpyridine-3,5-dicarboxylate

3-methyl 5-(1-methylethyl) 2-(fluoromethyl)-6-<(2,3,5,9b-tetrahydro-5-oxo-oxazolo<2,3-a>isoindol-9b-yl)methyl>-pyridine-3,5-dicarboxylate
117752-01-9

3-methyl 5-(1-methylethyl) 2-(fluoromethyl)-6-<(2,3,5,9b-tetrahydro-5-oxo-oxazolo<2,3-a>isoindol-9b-yl)methyl>-pyridine-3,5-dicarboxylate

Conditions
Conditions Yield
With sodium hydride; Yield given. Multistep reaction. Further byproducts given; 1.) DMF, 0 deg C, 2.) DMF, 20 deg C, 3 h;
61%
48%
53%

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;