4-Fluorobenzenesulfonyl chloride

• CAS: 349-88-2
• Catalog Number: ACM349882
• Category: Aryl Fluorinated Building Blocks
• Molecular Weight: 194.61
• Molecular Formula: C₇H₇FN₂S
• Hazard Statements: H302-H312-H315-H319-H332-H335
• RIDADR: UN 2811 6.1 / PGIII
• Symbol: GHS07

Custom Q&A

What is the chemical formula of 4-Fluorobenzenesulfonyl chloride?

The chemical formula of 4-Fluorobenzenesulfonyl chloride is C6H4ClFO2S.

What is the molecular weight of 4-Fluorobenzenesulfonyl chloride?

The molecular weight of 4-Fluorobenzenesulfonyl chloride is 194.61 g/mol.

What is the IUPAC name of 4-Fluorobenzenesulfonyl chloride?

The IUPAC name of 4-Fluorobenzenesulfonyl chloride is 4-fluorobenzenesulfonyl chloride.

What is the InChI of 4-Fluorobenzenesulfonyl chloride?

The InChI of 4-Fluorobenzenesulfonyl chloride is
InChI=1S/C6H4ClFO2S/c7-11(9,10)6-3-1-5(8)2-4-6/h1-4H.

What is the InChIKey of 4-Fluorobenzenesulfonyl chloride?

The InChIKey of 4-Fluorobenzenesulfonyl chloride is BFXHJFKKRGVUMU-UHFFFAOYSA-N.

What is the CAS number of 4-Fluorobenzenesulfonyl chloride?

The CAS number of 4-Fluorobenzenesulfonyl chloride is 349-88-2.

What is the European Community (EC) Number of 4-Fluorobenzenesulfonyl chloride?

The European Community (EC) Number of 4-Fluorobenzenesulfonyl chloride is 206-493-0.

What is the UNII of 4-Fluorobenzenesulfonyl chloride?

The UNII of 4-Fluorobenzenesulfonyl chloride is 2M9GLL38TN.

What is the molecular weight of 4-Fluorobenzenesulfonyl chloride computed by PubChem?

The molecular weight of 4-Fluorobenzenesulfonyl chloride computed by PubChem is 194.61 g/mol.

Is 4-Fluorobenzenesulfonyl chloride a canonicalized compound?

Yes, 4-Fluorobenzenesulfonyl chloride is a canonicalized compound.

Synthetic Use

Downstream Synthesis Route 1

• 462-06-6
• 349-88-2

• 383-29-9

Reference: [1] Tetrahedron Letters, 2004, vol. 45, # 7, p. 1499 - 1501
[2] Chemische Berichte, 1953, vol. 86, p. 172,180

Downstream Synthesis Route 2

• 349-88-2

• 371-42-6

Reference: [1] Journal of Sulfur Chemistry, 2012, vol. 33, # 2, p. 179 - 185
[2] Synthetic Communications, 2012, vol. 42, # 16, p. 2432 - 2439
[3] Acta Chimica Academiae Scientiarum Hungaricae, 1954, vol. 4, p. 111,115
[4] Chemische Berichte, 1953, vol. 86, p. 172,180
[5] Collection of Czechoslovak Chemical Communications, 1975, vol. 40, # 3, p. 719 - 737

Downstream Synthesis Route 3

• 349-88-2

• 352-33-0
• 383-29-9
• 398-23-2
• 404-38-6

Reference: [1] Tetrahedron Letters, 2005, vol. 46, # 42, p. 7125 - 7128

Downstream Synthesis Route 4

• 462-06-6
• 349-88-2

• 383-29-9

Reference: [1]Tetrahedron Letters,2004,vol. 45,p. 1499 - 1501
[2]Chemische Berichte,1953,vol. 86,p. 172,180

Downstream Synthesis Route 5

• 349-88-2
• 402-46-0

• 1495-58-5

Reference: [1]Collection of Czechoslovak Chemical Communications,1996,vol. 61,p. 1205 - 1214
[2]Zhurnal Obshchei Khimii,1959,vol. 29,p. 3602,3605; engl. Ausg. S. 3563, 3565

Downstream Synthesis Route 6

• 349-88-2

• 402-46-0

Reference: [1]Liebigs Annales,1997,p. 141 - 154

* For details of the synthesis route, please refer to the original source to ensure accuracy.