2367-82-0 | 1,2,3,5-Tetrafluorobenzene

Packsize	Purity	Availability	Price	Discounted Price
250mg	98%	in stock	$14.00	$10.00
1g	98%	in stock	$20.00	$14.00
5g	98%	in stock	$65.00	$45.00
25g	98%	in stock	$282.00	$198.00
100g	98%	in stock	$1,006.00	$705.00

Description

• Catalog Number: AB24336
• Chemical Name: 1,2,3,5-Tetrafluorobenzene
• CAS Number: 2367-82-0
• Molecular Formula: C6H2F4
• Molecular Weight: 150.0736928
• MDL Number: MFCD00000302
• SMILES: Fc1cc(F)c(c(c1)F)F

Computed Properties

• Complexity: 104
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 10
• Hydrogen Bond Acceptor Count: 4
• XLogP3: 2.4

Upstream Synthesis Route

1,2,3,5-Tetrafluorobenzene is a valuable compound in chemical synthesis due to its unique properties and reactivity. Its four fluorine atoms make it an excellent source of fluorine in organic reactions, allowing for the introduction of this important element into various molecules. This compound is commonly used as a precursor in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. In particular, 1,2,3,5-Tetrafluorobenzene is often employed in the preparation of fluorinated materials, which are essential in industries such as materials science and electronics. Its versatility and reliability make it a valuable building block in organic chemistry, enabling the creation of new and innovative compounds with enhanced properties.

Literature

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  Dalton transactions (Cambridge, England : 2003) 20120714

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  Organic & biomolecular chemistry 20090321

• Selective C-F bond activation of tetrafluorobenzenes by nickel(0) with a nitrogen donor analogous to N-heterocyclic carbenes.

  Angewandte Chemie (International ed. in English) 20090101

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  Organic & biomolecular chemistry 20070821

• Theoretical investigation of in-plane hydrogen-bonded complexes of ammonia with partially substituted fluorobenzenes.

  The journal of physical chemistry. A 20070412

• Dehydro[12]- and -[18]annulenes fused with tetrafluorobenzene: synthesis, electronic properties, packing structures, and reactivity in the solid state.

  The Journal of organic chemistry 20020823

• Photoreductive dehalogenation of halogenated benzene derivatives using ZnS or CdS nanocrystallites as photocatalysts.

  Environmental science & technology 20010101