2,4-Heptadiyn-1-ol, 6-methoxy-6-methyl-

Base Information

Chemical Name:2,4-Heptadiyn-1-ol, 6-methoxy-6-methyl-
CAS No.:60214-11-1
Molecular Formula:C9H12O2
Molecular Weight:152.193
Hs Code.:
DSSTox Substance ID:DTXSID70433684
Wikidata:Q82247888

Synonyms:2,4-Heptadiyn-1-ol, 6-methoxy-6-methyl-;60214-11-1;SCHEMBL9251583;DTXSID70433684;MOIUWGZCJWCQNM-UHFFFAOYSA-N;6-methoxy-6-methyl-2,4-heptadiyn-1-ol

Suppliers and Price of 2,4-Heptadiyn-1-ol, 6-methoxy-6-methyl-

Supply Marketing:

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

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of 2,4-Heptadiyn-1-ol, 6-methoxy-6-methyl-

Chemical Property:

XLogP3:0.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:152.083729621
Heavy Atom Count:11
Complexity:238

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C#CC#CCO)OC

Technology Process of 2,4-Heptadiyn-1-ol, 6-methoxy-6-methyl-

There total 1 articles about 2,4-Heptadiyn-1-ol, 6-methoxy-6-methyl- 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:

: 2060-25-5
3-bromoprop-2-yn-1-ol

: 13994-57-5
3-methoxy-3-methylbut-1-yne

: 60214-11-1
3-methoxy-3-methyl-2,4-heptadiyn-1-ol

Guidance literature:: With hydroxylamine hydrochloride; isopropylamine; copper(l) chloride; In methanol;

Reference yield:

: 60214-11-1
3-methoxy-3-methyl-2,4-heptadiyn-1-ol

: N-ethyl-N-(6-methoxy-6-methyl-2,4-heptadiynyl)-3-<((2-methylphenyl)dimethylsilyl)methoxy>benzylamine

Guidance literature:: Multi-step reaction with 2 steps

1: 100 percent / triethylamine / tetrahydrofuran / 1 h / Ambient temperature

2: triethylamine / dimethylformamide / 15 h / Ambient temperature

With triethylamine; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1021/jm00017a004