Oxirane, 3-[5-(4-azido-2-nitrophenoxy)-3-methyl-3-pentenyl]-2,2-dimeth yl-, (E)-.+/-.-

Base Information

Chemical Name:Oxirane, 3-[5-(4-azido-2-nitrophenoxy)-3-methyl-3-pentenyl]-2,2-dimeth yl-, (E)-.+/-.-
CAS No.:106929-47-9
Molecular Formula:C16H20 N4 O4
Molecular Weight:0
Hs Code.:
Mol file:106929-47-9.mol

Synonyms:Oxirane,3-[5-(4-azido-2-nitrophenoxy)-3-methyl-3-pentenyl]-2,2-dimethyl-, (E)- (9CI);Oxirane, 3-[5-(4-azido-2-nitrophenoxy)-3-methyl-3-pentenyl]-2,2-dimethyl-,(E)-(?à)-

Suppliers and Price of Oxirane, 3-[5-(4-azido-2-nitrophenoxy)-3-methyl-3-pentenyl]-2,2-dimeth yl-, (E)-.+/-.-

Supply Marketing:

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

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Chemical Property of Oxirane, 3-[5-(4-azido-2-nitrophenoxy)-3-methyl-3-pentenyl]-2,2-dimeth yl-, (E)-.+/-.-

Chemical Property:

PSA：117.33000
LogP:4.79526

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of Oxirane, 3-[5-(4-azido-2-nitrophenoxy)-3-methyl-3-pentenyl]-2,2-dimeth yl-, (E)-.+/-.-

There total 3 articles about Oxirane, 3-[5-(4-azido-2-nitrophenoxy)-3-methyl-3-pentenyl]-2,2-dimeth yl-, (E)-.+/-.- 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: 58.0%

: 106929-46-8
p-azido-o-nitrophenyl geranyl ether

: 106929-47-9
(2E)-1-(4-azido-2-nitrophenoxy)-6,7-epoxy-3,7-dimethyl-2-octene

Guidance literature:: With 3-chloro-benzenecarboperoxoic acid; In chloroform; at -5 ℃; for 3h;

Reference yield:

: 106-24-1
Geraniol

: 106929-47-9
(2E)-1-(4-azido-2-nitrophenoxy)-6,7-epoxy-3,7-dimethyl-2-octene

Guidance literature:: Multi-step reaction with 2 steps

1: 76 percent / t-BuOK / tetrahydrofuran / 14 h / Ambient temperature

2: 58 percent / 85percent m-chloroperbenzoic acid / CHCl₃ / 3 h / -5 °C

With potassium tert-butylate; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; chloroform;

Reference yield:

: 28166-06-5
4-fluoro-3-nitrophenylazide

: 106929-47-9
(2E)-1-(4-azido-2-nitrophenoxy)-6,7-epoxy-3,7-dimethyl-2-octene

Guidance literature:: Multi-step reaction with 2 steps

1: 76 percent / t-BuOK / tetrahydrofuran / 14 h / Ambient temperature

2: 58 percent / 85percent m-chloroperbenzoic acid / CHCl₃ / 3 h / -5 °C

With potassium tert-butylate; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; chloroform;