[(tert-Butoxymethoxy)methyl]benzene

Base Information

Chemical Name:[(tert-Butoxymethoxy)methyl]benzene
CAS No.:66922-43-8
Molecular Formula:C₁₂H₁₈O₂
Molecular Weight:194.274
Hs Code.:
DSSTox Substance ID:DTXSID10533576
Wikidata:Q82406962

Synonyms:66922-43-8;[(tert-Butoxymethoxy)methyl]benzene;DTXSID10533576

Suppliers and Price of [(tert-Butoxymethoxy)methyl]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 [(tert-Butoxymethoxy)methyl]benzene

Chemical Property:

XLogP3:2.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:5
Exact Mass:194.130679813
Heavy Atom Count:14
Complexity:143

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(C)(C)OCOCC1=CC=CC=C1

Technology Process of [(tert-Butoxymethoxy)methyl]benzene

There total 4 articles about [(tert-Butoxymethoxy)methyl]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: 70.0%

: 30379-55-6
benzyloxyacetic acid

: 865-47-4
potassium tert-butylate

: 66922-43-8
formaldehyde benzyl t-butyl acetal

: 88920-28-9
benzyloxymethyl benzyloxyacetate

Guidance literature:: With Iodine monochloride; In tetrachloromethane; 1.) 15 min, 2.) irradiation, 18 deg C, 3 h;

Reference yield:

: 1634-04-4
tert-butyl methyl ether

: 66922-43-8
formaldehyde benzyl t-butyl acetal

Guidance literature:: Multi-step reaction with 2 steps

1: N-chloro-succinimide / CCl₄ / Irradiation

2: Et₃N / tetrahydrofuran

With N-chloro-succinimide; triethylamine; In tetrahydrofuran; tetrachloromethane;
DOI:10.1021/jo00414a037