(2-Chloro-1,1-diethoxyethyl)benzene

Base Information

Chemical Name:(2-Chloro-1,1-diethoxyethyl)benzene
CAS No.:109481-85-8
Molecular Formula:C₁₂H₁₇ClO₂
Molecular Weight:228.719
Hs Code.:
DSSTox Substance ID:DTXSID10546040
Wikidata:Q82423738
Mol file:109481-85-8.mol

Synonyms:(2-Chloro-1,1-diethoxyethyl)benzene;109481-85-8;DTXSID10546040

Suppliers and Price of (2-Chloro-1,1-diethoxyethyl)benzene

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of (2-Chloro-1,1-diethoxyethyl)benzene

Chemical Property:

XLogP3:2.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:6
Exact Mass:228.0917075
Heavy Atom Count:15
Complexity:161

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC(CCl)(C1=CC=CC=C1)OCC

Technology Process of (2-Chloro-1,1-diethoxyethyl)benzene

There total 3 articles about (2-Chloro-1,1-diethoxyethyl)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: 77.0%

: 929618-08-6
(E)-2-chloro-1-ethoxystyrene

: 64-17-5
ethanol

: 109481-85-8
phenacyl chloride diethyl acetal

Guidance literature:: With hydrogenchloride; at 20 ℃; for 0.166667h;
DOI:10.1002/ejoc.200600863

Reference yield:

: 591-51-5
phenyllithium

: 109481-85-8
phenacyl chloride diethyl acetal

Guidance literature:: Multi-step reaction with 2 steps

1: DME / diethyl ether / 0.25 h / -60 °C

2: 77 percent / HCl / 0.17 h / 20 °C

With hydrogenchloride; 1,2-dimethoxyethane; In diethyl ether;
DOI:10.1002/ejoc.200600863