Cyclohexanesulfonyl chloride

• CAS: 4837-38-1
• Catalog Number: ACM4837381
• Category: Other Products
• Molecular Weight: 182.67
• Molecular Formula: C₆H₁₁ClO₂S
• Synonyms: Cyclohexanesulphonyl chloride 90%;Cyclohexanesulphonylchloride90%;Cyclohexanesulfonyl chloride;Cyclohexylsulfonyl chloride;Cyclohexanesulfonyl chloride,Cyclohexylsulfonyl chloride;(Chlorosulphonyl)cyclohexane;Cyclohexanesulfonyl chloride 90%
• Flash Point: >230°F
• Density: 1.259g/mL at 25°C
• Hazard Statements: C
• Safety Description: 26-36/37/39-45
• Supplemental Hazard Statements: H314
• Symbol: GHS05

Custom Q&A

What is the molecular formula of Cyclohexanesulfonyl chloride?

The molecular formula of Cyclohexanesulfonyl chloride is C6H11ClO2S.

What is the molecular weight of Cyclohexanesulfonyl chloride?

The molecular weight of Cyclohexanesulfonyl chloride is 182.67 g/mol.

What is the IUPAC name of Cyclohexanesulfonyl chloride?

The IUPAC name of Cyclohexanesulfonyl chloride is cyclohexanesulfonyl chloride.

What is the InChI key of Cyclohexanesulfonyl chloride?

The InChI key of Cyclohexanesulfonyl chloride is MJWVCJUSRGLHFO-UHFFFAOYSA-N.

How many hydrogen bond acceptor counts are there in Cyclohexanesulfonyl chloride?

There are 2 hydrogen bond acceptor counts in Cyclohexanesulfonyl chloride.

How many rotatable bond counts are there in Cyclohexanesulfonyl chloride?

There is 1 rotatable bond count in Cyclohexanesulfonyl chloride.

What is the topological polar surface area of Cyclohexanesulfonyl chloride?

The topological polar surface area of Cyclohexanesulfonyl chloride is 42.5 Ų.

Is Cyclohexanesulfonyl chloride a canonicalized compound?

Yes, Cyclohexanesulfonyl chloride is a canonicalized compound.

What is the CAS number of Cyclohexanesulfonyl chloride?

The CAS number of Cyclohexanesulfonyl chloride is 4837-38-1.

What is the exact mass and monoisotopic mass of Cyclohexanesulfonyl chloride?

The exact mass and monoisotopic mass of Cyclohexanesulfonyl chloride are both 182.0168285 g/mol.

Synthetic Use

Upstream Synthesis Route 1

• 110-82-7

• 4837-38-1

Reference: [1]Khanna, Vibha; Tamilselvan, Pitchiah; Kalra, Swinder Jeet Singh; Iqbal, Javed
[Tetrahedron Letters, 1994, vol. 35, # 32, p. 5935 - 5938]
[2]Current Patent Assignee: Du Pont de Nemours & Co. - US2174509, 1938, A
[3]Schneider
[United States Atomic Energy Commission, ANL-5863<1958>41]

Upstream Synthesis Route 2

• 2550-40-5

• 4837-38-1

Reference: [1]Synlett,2009,p. 2773 - 2776

Upstream Synthesis Route 3

• 10039-63-1

• 4837-38-1

Reference: [1]Nishiguchi, Atsuko; Maeda, Kazuhiro; Miki, Shokyo
[Synthesis, 2006, # 24, p. 4131 - 4134]
[2]Bordwell; Hewett
[Journal of Organic Chemistry, 1957, vol. 22, p. 980]

Downstream Synthesis Route 1

• 7664-41-7
• 4837-38-1

• 2438-38-2

Reference: [1] Patent: WO2008/101979, 2008, A1, . Location in patent: Page/Page column 88

Downstream Synthesis Route 2

• 4837-38-1

• 2438-38-2

Reference: [1] Bioorganic and Medicinal Chemistry, 2014, vol. 22, # 11, p. 3030 - 3054

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