1-Chloro-10-iododecane

Base Information

Chemical Name:1-Chloro-10-iododecane
CAS No.:57152-87-1
Molecular Formula:C10H20ClI
Molecular Weight:302.62327
Hs Code.:
DSSTox Substance ID:DTXSID30472251
Nikkaji Number:J1.337.020F
Wikidata:Q82301069

Synonyms:1-CHLORO-10-IODODECANE;57152-87-1;SCHEMBL2733952;DTXSID30472251

Suppliers and Price of 1-Chloro-10-iododecane

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 12 raw suppliers

Chemical Property of 1-Chloro-10-iododecane

Chemical Property:

XLogP3:6.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:9
Exact Mass:302.02983
Heavy Atom Count:12
Complexity:76.2

Purity/Quality:: 99.0% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C(CCCCCI)CCCCCl

Technology Process of 1-Chloro-10-iododecane

There total 4 articles about 1-Chloro-10-iododecane 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: 86.0%

: 51309-10-5
10-chlorodecanol

: 57152-87-1
1-chloro-10-iododecane

Guidance literature:: With iodine; triphenylphosphine; In dichloromethane;
DOI:10.1016/j.tetlet.2015.02.048

Reference yield:

: 2162-98-3
1,10-dichlorodecane

: 57152-87-1
1-chloro-10-iododecane

Guidance literature:: With acetone; sodium iodide;
DOI:10.1021/ja01150a087

Reference yield:

: 112-47-0
1,10-Decanediol

: 57152-87-1
1-chloro-10-iododecane

Guidance literature:: Multi-step reaction with 2 steps

1: pyridine; thionyl chloride

2: acetone; sodium iodide

With pyridine; thionyl chloride; acetone; sodium iodide;
DOI:10.1021/ja01150a087