2-Diallylaminomethyl-phenol

Base Information

Chemical Name:2-Diallylaminomethyl-phenol
CAS No.:60405-97-2
Molecular Formula:C13H17NO
Molecular Weight:203.284
Hs Code.:
DSSTox Substance ID:DTXSID00398671
Wikidata:Q82200783

Synonyms:2-diallylaminomethyl-phenol;60405-97-2;2-[(diprop-2-en-1-ylamino)methyl]phenol;SCHEMBL4942839;DTXSID00398671;GGCJPFXOYISGOD-UHFFFAOYSA-N;STK029545;AKOS005380752

Suppliers and Price of 2-Diallylaminomethyl-phenol

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
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Total 0 raw suppliers

Chemical Property of 2-Diallylaminomethyl-phenol

Chemical Property:

XLogP3:2.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:6
Exact Mass:203.131014166
Heavy Atom Count:15
Complexity:193

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C=CCN(CC=C)CC1=CC=CC=C1O

Technology Process of 2-Diallylaminomethyl-phenol

There total 2 articles about 2-Diallylaminomethyl-phenol 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: 82.0%

: 177780-96-0
2-[N-(prop-2'-enyl)aminomethyl]phenol

: 106-95-6
allyl bromide

: 60405-97-2
2-((diallylamino)methyl)phenol

Guidance literature:: With potassium carbonate; In acetonitrile; at 20 ℃;
DOI:10.1021/ol017240j

Reference yield: 73.0%

: 951164-80-0
N-allyl-N-(methoxymethyl)prop-2-en-1-amine

: 108-95-2,27073-41-2
phenol

: 60405-97-2
2-((diallylamino)methyl)phenol

Guidance literature:: With trifluoroacetic acid; In dichloromethane; at 25 ℃; for 12h; chemoselective reaction; Inert atmosphere; Molecular sieve;
DOI:10.1039/d1ob00820j