2-Phenyl-ethanesulfonyl chloride

• CAS: 4025-71-2
• Catalog Number: ACM4025712
• Category: Other Products
• Molecular Weight: 204.67
• Molecular Formula: C₈H₉ClO₂S
• Synonyms: 2-PHENYL-ETHANESULFONYL CHLORIDE;2-Phenyl-ethanesulfonyl chloride ,95%;2-phenylethane-1-sulfonyl chloride

Custom Q&A

What is the molecular formula of 2-Phenyl-ethanesulfonyl chloride?

The molecular formula of 2-Phenyl-ethanesulfonyl chloride is C8H9ClO2S.

When was 2-Phenyl-ethanesulfonyl chloride created and modified in PubChem?

2-Phenyl-ethanesulfonyl chloride was created on July 19, 2005, and last modified on December 30, 2023.

What is the molecular weight of 2-Phenyl-ethanesulfonyl chloride?

The molecular weight of 2-Phenyl-ethanesulfonyl chloride is 204.67 g/mol.

What is the IUPAC name for 2-Phenyl-ethanesulfonyl chloride?

The IUPAC name for 2-Phenyl-ethanesulfonyl chloride is 2-phenylethanesulfonyl chloride.

What is the InChIKey for 2-Phenyl-ethanesulfonyl chloride?

The InChIKey for 2-Phenyl-ethanesulfonyl chloride is LKFNLHZZPHHFEC-UHFFFAOYSA-N.

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

2-Phenyl-ethanesulfonyl chloride has 2 hydrogen bond acceptor counts.

What is the exact mass of 2-Phenyl-ethanesulfonyl chloride?

The exact mass of 2-Phenyl-ethanesulfonyl chloride is 204.0011784 g/mol.

How many rotatable bond counts does 2-Phenyl-ethanesulfonyl chloride have?

2-Phenyl-ethanesulfonyl chloride has 3 rotatable bond counts.

Is 2-Phenyl-ethanesulfonyl chloride a canonicalized compound?

Yes, 2-Phenyl-ethanesulfonyl chloride is a canonicalized compound according to PubChem.

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

The topological polar surface area of 2-Phenyl-ethanesulfonyl chloride is 42.5 Ų.

Synthetic Use

Upstream Synthesis Route 1

• 4410-99-5

• 4025-71-2

Reference: [1] Bioorganic and Medicinal Chemistry Letters, 2002, vol. 12, # 8, p. 1181 - 1184

Upstream Synthesis Route 2

• 103-63-9

• 4025-71-2

Reference: [1] Bioorganic and Medicinal Chemistry, 2017, vol. 25, # 14, p. 3861 - 3870

Upstream Synthesis Route 3

• 6326-49-4

• 4025-71-2

Reference: [1] Synthesis (Germany), 2013, vol. 45, # 12, p. 1675 - 1682
[2] Synlett, 2013, vol. 24, # 16, p. 2165 - 2169

Downstream Synthesis Route 1

• 4025-71-2

• 2924-68-7

Reference: [1]Journal of the American Chemical Society,1963,vol. 85,p. 997 - 1000

Downstream Synthesis Route 2

• 91-21-4
• 4025-71-2

• 143769-81-7

Reference: [1]Journal of Heterocyclic Chemistry,1992,vol. 29,p. 859 - 866

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