Perfluorocyclohexanecarbonyl chloride

Base Information

• Chemical Name: Perfluorocyclohexanecarbonyl chloride
• CAS No.: 58816-79-8
• Molecular Formula: C7Cl F11 O
• Molecular Weight: 344.512
• Hs Code.: 2916200090
• European Community (EC) Number: 671-786-6
• DSSTox Substance ID: DTXSID70380760
• Nikkaji Number: J3.118.266B
• Wikidata: Q82171195
• Mol file: 58816-79-8.mol

Synonyms:58816-79-8;Perfluorocyclohexanecarbonyl chloride;1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclohexane-1-carbonyl Chloride;undecafluorocyclohexanecarbonyl chloride;perfluorocyclohexyl carboxylic acid chloride;SCHEMBL8448028;DTXSID70380760;JBOWALSHDVHATH-UHFFFAOYSA-N;MFCD00156086;AKOS005173370;FT-0683459;Undecafluorocyclohexanecarboxylic acid chloride;A832031;A937791;1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclohexanecarbonyl chloride;1,2,2,3,3,4,4,5,5,6,6-undecafluoro-1-cyclohexanecarbonyl chloride;1,2,2,3,3,4,4,5,5,6,6-undecakis(fluoranyl)cyclohexane-1-carbonyl chloride

Chemical Property of Perfluorocyclohexanecarbonyl chloride

Chemical Property:

• Vapor Pressure: 6.53mmHg at 25°C
• Boiling Point: 95-96°C
• Flash Point: 37.9°C
• PSA: 17.07000
• Density: 1.77g/cm³
• LogP: 3.65020
• XLogP3: 4.1
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 12
• Rotatable Bond Count: 1
• Exact Mass: 343.9462021
• Heavy Atom Count: 20
• Complexity: 426

Purity/Quality:

98%Min ^*data from raw suppliers

Perfluorocyclohexanecarbonylchloride 97% ^*data from reagent suppliers

Safty Information:

• Hazard Codes: C
• Statements: 34
• Safety Statements: 26-28-36/37/39

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C(=O)(C1(C(C(C(C(C1(F)F)(F)F)(F)F)(F)F)(F)F)F)Cl
• Uses: Undecafluorocyclohexanecarbonyl Chloride is used in preparation of Ester group-connected Vinyl Ether-terminated Organofluorine cation monomer.

Technology Process of Perfluorocyclohexanecarbonyl chloride

There total 3 articles about Perfluorocyclohexanecarbonyl chloride which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclohexanecarbonyl fluoride (6588-63-2) → 1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclohexanecarbonyl chloride (58816-79-8)

Guidance literature:

With zinc(II) chloride; at 185 ℃;

DOI:10.1021/jo00875a007

Reference yield:

→ 1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclohexanecarbonyl chloride (58816-79-8)

Guidance literature:

/BRN= 63039/ (Py.), Cl2C=O (86-120grad, 10h);

Reference yield:

→ Epilupinin (486-70-4,486-71-5,486-72-6,7635-60-1,10159-79-2,10248-30-3,112065-89-1)

Guidance literature:

1-Carbethoxy-4-chinolizidon (23), Red.;

DOI:10.1016/S0040-4020(01)97140-6

upstream raw materials:

1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclohexanecarbonyl fluoride

Downstream raw materials:

N'-perfluorocyclohexancarbonyl-perfluorocyclohexancarbohydrazide

3-oxo-2-(pyrrolidin-(2Z)-ylidene)-3-undecafluorocyclohexylpropionitrile