2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11-icosafluoroundecanoyl Chloride

Base Information

• Chemical Name: 2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11-icosafluoroundecanoyl Chloride
• CAS No.: 2248-93-3
• Molecular Formula: C11H Cl F20 O
• Molecular Weight: 564.55
• Hs Code.: 2915900090
• DSSTox Substance ID: DTXSID90380060
• Nikkaji Number: J1.060.114B
• Wikidata: Q82170088
• Mol file: 2248-93-3.mol

Synonyms:2248-93-3;11H-Perfluoroundecanoyl chloride;11h-eicosafluoroundecanoyl chloride;2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11-icosafluoroundecanoyl Chloride;SCHEMBL5705237;DTXSID90380060;LFSNWCISDMSHBB-UHFFFAOYSA-N;11H-PERFLUOROUNDECANOYLCHLORIDE;AKOS016016010;FT-0607221;A816229;2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11-eicosafluoroundecanoyl chloride;2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11-Icosafluoroundecanoic acid chloride;2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11-icosakis(fluoranyl)undecanoyl chloride;Undecanoyl chloride,2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11-eicosafluoro-

Chemical Property of 2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11-icosafluoroundecanoyl Chloride

Chemical Property:

• Melting Point: 54-56°C
• Boiling Point: 209.3°Cat760mmHg
• Flash Point: 80.4°C
• PSA: 17.07000
• Density: 1.719g/cm³
• LogP: 6.73460
• Sensitive.: Moisture Sensitive
• XLogP3: 7.7
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 21
• Rotatable Bond Count: 10
• Exact Mass: 563.9396556
• Heavy Atom Count: 33
• Complexity: 753

Purity/Quality:

99% ^*data from raw suppliers

11H-Eicosafluoroundecanoyl chloride 92% ^*data from reagent suppliers

Safty Information:

• Hazard Codes: C
• Statements: 34
• Safety Statements: 26-36/37/39-45

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C(C(C(C(C(C(C(C(C(C(C(=O)Cl)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F

Technology Process of 2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11-icosafluoroundecanoyl Chloride

There total 1 articles about 2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11-icosafluoroundecanoyl 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:

→ 11H-perfluoroundecanoyl chloride (2248-93-3)

Guidance literature:

SOCl2, Saeure;

Reference yield:

11H-perfluoroundecanoyl chloride (2248-93-3) + benzene (71-43-2,26181-88-4,54682-86-9,13967-78-7,174973-66-1) → <10-H-perfluor-decyl>-benzol (1691-50-5)

Guidance literature:

tetracarbonyl nickel; at 150 ℃; for 8h;

DOI:10.1021/ja01504a025

Reference yield:

11H-perfluoroundecanoyl chloride (2248-93-3) → Perfluornonan-1.9-dicarbonsaeuredimethylester (22116-91-2)

Guidance literature:

Multi-step reaction with 2 steps

1: NO₂, Cl₂

2: (esterification)

With chlorine; Nitrogen dioxide;

DOI:10.1016/S0040-4039(00)75950-8

Downstream raw materials:

<10-H-perfluor-decyl>-benzol

11H-Eicosafluor-1-phenyl-undecan-1-on

Perfluornonan-1.9-dicarbonsaeuredimethylester