(E)-14-(4-(phenyldiazenyl)phenoxy)-3,6,9,12-tetraoxatetradecan-1-oic acid

Base Information

Chemical Name:(E)-14-(4-(phenyldiazenyl)phenoxy)-3,6,9,12-tetraoxatetradecan-1-oic acid
CAS No.:1352645-85-2
Molecular Formula:C₂₂H₂₈N₂O₇
Molecular Weight:432.474
Hs Code.:

Synonyms:(E)-14-(4-(phenyldiazenyl)phenoxy)-3,6,9,12-tetraoxatetradecan-1-oic acid

Suppliers and Price of (E)-14-(4-(phenyldiazenyl)phenoxy)-3,6,9,12-tetraoxatetradecan-1-oic acid

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

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Chemical Property of (E)-14-(4-(phenyldiazenyl)phenoxy)-3,6,9,12-tetraoxatetradecan-1-oic acid

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Technology Process of (E)-14-(4-(phenyldiazenyl)phenoxy)-3,6,9,12-tetraoxatetradecan-1-oic acid

There total 1 articles about (E)-14-(4-(phenyldiazenyl)phenoxy)-3,6,9,12-tetraoxatetradecan-1-oic acid 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: 87.0%

: 1352645-84-1
(E)-ethyl 14-(4-(phenyldiazenyl)phenoxy)-3,6,9,12-tetraoxatetradecan-1-oate

: 1352645-85-2
(E)-14-(4-(phenyldiazenyl)phenoxy)-3,6,9,12-tetraoxatetradecan-1-oic acid

Guidance literature:: With sodium hydroxide; In methanol; water; at 0 - 20 ℃; Inert atmosphere;
DOI:10.1002/anie.201103707

Reference yield: 24.0%

: 1352645-85-2
(E)-14-(4-(phenyldiazenyl)phenoxy)-3,6,9,12-tetraoxatetradecan-1-oic acid

: 114459-62-0
tri-Boc-spermine

: 1352645-86-3
(E)-tert-butyl (4-((tert-butoxycarbonyl)(3-((tert-butoxycarbonyl)amino)propyl)amino)-butyl)(14-oxo-1-(4-(phenyldiazenyl)phenoxy)-3,6,9,12-tetraoxa-15-azaoctadecan-18-yl)carbamate

Guidance literature:: With benzotriazol-1-ol; triethylamine; dicyclohexyl-carbodiimide; In ethyl acetate; at 0 - 20 ℃; for 49h; Inert atmosphere;
DOI:10.1002/anie.201103707