Structure

2-Fluorobenzenesulfonyl chloride

CAS
2905-21-7
Catalog Number
ACM2905217
Category
Aryl Fluorinated Building Blocks
Molecular Weight
194.61
Molecular Formula
C7H7FN2O

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Specification

Hazard Statements
H315-H319-H335
RIDADR
UN 2811 6.1 / PGIII
Symbol
GHS07
What is the molecular formula of 2-Fluorobenzenesulfonyl chloride?

The molecular formula of 2-Fluorobenzenesulfonyl chloride is C6H4ClFO2S.

What is the molecular weight of 2-Fluorobenzenesulfonyl chloride?

The molecular weight of 2-Fluorobenzenesulfonyl chloride is 194.61 g/mol.

What is the IUPAC name of 2-Fluorobenzenesulfonyl chloride?

The IUPAC name of 2-Fluorobenzenesulfonyl chloride is 2-fluorobenzenesulfonyl chloride.

What is the InChIKey of 2-Fluorobenzenesulfonyl chloride?

The InChIKey of 2-Fluorobenzenesulfonyl chloride is ZSZKAQCISWFDCQ-UHFFFAOYSA-N.

How many hydrogen bond donor counts does 2-Fluorobenzenesulfonyl chloride have?

2-Fluorobenzenesulfonyl chloride has 0 hydrogen bond donor counts.

How many hydrogen bond acceptor counts does 2-Fluorobenzenesulfonyl chloride have?

2-Fluorobenzenesulfonyl chloride has 3 hydrogen bond acceptor counts.

What is the topological polar surface area of 2-Fluorobenzenesulfonyl chloride?

The topological polar surface area of 2-Fluorobenzenesulfonyl chloride is 42.5 Å^2.

How many rotatable bond counts does 2-Fluorobenzenesulfonyl chloride have?

2-Fluorobenzenesulfonyl chloride has 1 rotatable bond count.

Is 2-Fluorobenzenesulfonyl chloride a canonicalized compound?

Yes, 2-Fluorobenzenesulfonyl chloride is a canonicalized compound.

When was 2-Fluorobenzenesulfonyl chloride last modified?

2-Fluorobenzenesulfonyl chloride was last modified on December 23, 2023.

Upstream Synthesis Route 1

  • 2557-78-0
  • 2905-21-7

Reference: [1] Green Chemistry, 2017, vol. 19, # 9, p. 2286 - 2295

Upstream Synthesis Route 2

  • 348-54-9
  • 2905-21-7

Reference: [1] Recueil des Travaux Chimiques des Pays-Bas, 1965, vol. 84, p. 24 - 30

Downstream Synthesis Route 1

  • 2905-21-7
  • 30058-40-3

Reference: [1] Bioorganic and Medicinal Chemistry Letters, 2014, vol. 24, # 9, p. 2222 - 2225
[2] Green Chemistry, 2015, vol. 17, # 3, p. 1395 - 1399

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

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