4-tert-Butyl-1,2-bis(3-chloropropoxy)benzene

Base Information

Chemical Name:4-tert-Butyl-1,2-bis(3-chloropropoxy)benzene
CAS No.:83557-02-2
Molecular Formula:C16H24Cl2O2
Molecular Weight:319.271
Hs Code.:
DSSTox Substance ID:DTXSID50535413
Wikidata:Q82409713

Synonyms:4-tert-Butyl-1,2-bis(3-chloropropoxy)benzene;83557-02-2;SCHEMBL10989919;DTXSID50535413

Suppliers and Price of 4-tert-Butyl-1,2-bis(3-chloropropoxy)benzene

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 1 raw suppliers

Chemical Property of 4-tert-Butyl-1,2-bis(3-chloropropoxy)benzene

Chemical Property:

XLogP3:5.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:9
Exact Mass:318.1153354
Heavy Atom Count:20
Complexity:253

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C)C1=CC(=C(C=C1)OCCCCl)OCCCCl

Technology Process of 4-tert-Butyl-1,2-bis(3-chloropropoxy)benzene

There total 3 articles about 4-tert-Butyl-1,2-bis(3-chloropropoxy)benzene 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: 76.0%

: 83557-01-1
1,2-bis(3-hydroxypropoxy)-4-t-butylbenzene

: 83557-02-2
1,2-Bis(3-chloropropoxy)-4-t-butylbenzene

Guidance literature:: With thionyl chloride; In pyridine; benzene; for 10h; Heating;
DOI:10.1246/bcsj.57.1976

Reference yield:

: 98-29-3
4-tert-Butylcatechol

: 83557-02-2
1,2-Bis(3-chloropropoxy)-4-t-butylbenzene

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) powdered potassium carbonate; 2.) KI / 1.) 70 deg C, 24 h, DMF; 2.) 70 deg C, 24 h

2: 76 percent / thionyl chloride / benzene; pyridine / 10 h / Heating

With thionyl chloride; potassium carbonate; potassium iodide; In pyridine; benzene;
DOI:10.1246/bcsj.57.1976