poly(oxyimidocarbonyloxy-p-phenylene(2-(hexyloxycarbonyl)ethylene)imino(2-(1-(benzyloxy)formamido)-1-oxotrimethylene)-p-phenylene)

Base Information

Chemical Name:poly(oxyimidocarbonyloxy-p-phenylene(2-(hexyloxycarbonyl)ethylene)imino(2-(1-(benzyloxy)formamido)-1-oxotrimethylene)-p-phenylene)
CAS No.:106755-33-3
Molecular Formula:C₃₄H₃₆N₄O₇
Molecular Weight:612.682
Hs Code.:
Mol file:106755-33-3.mol

Synonyms:poly(oxyimidocarbonyloxy-p-phenylene(2-(hexyloxycarbonyl)ethylene)imino(2-(1-(benzyloxy)formamido)-1-oxotrimethylene)-p-phenylene)

Suppliers and Price of poly(oxyimidocarbonyloxy-p-phenylene(2-(hexyloxycarbonyl)ethylene)imino(2-(1-(benzyloxy)formamido)-1-oxotrimethylene)-p-phenylene)

Supply Marketing:

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

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Chemical Property of poly(oxyimidocarbonyloxy-p-phenylene(2-(hexyloxycarbonyl)ethylene)imino(2-(1-(benzyloxy)formamido)-1-oxotrimethylene)-p-phenylene)

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
Density:1.227g/cm³

Purity/Quality:

Safty Information:

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Technology Process of poly(oxyimidocarbonyloxy-p-phenylene(2-(hexyloxycarbonyl)ethylene)imino(2-(1-(benzyloxy)formamido)-1-oxotrimethylene)-p-phenylene)

There total 4 articles about poly(oxyimidocarbonyloxy-p-phenylene(2-(hexyloxycarbonyl)ethylene)imino(2-(1-(benzyloxy)formamido)-1-oxotrimethylene)-p-phenylene) 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: 78.0%

: 506-68-3
bromocyane

: 106231-84-9
N-(N-benzyloxycarbonyl-L-tyrosyl)-L-tyrosine hexyl ester

: 104549-44-2,106755-33-3
Z-Tyr-Tyr-Hex-dicyanate

Guidance literature:: In ethyl acetate; at -10 - 10 ℃;
DOI:10.1021/ja00237a030

Reference yield:

: 1164-16-5
Z-L-Tyr-OH

: 104549-44-2,106755-33-3
Z-Tyr-Tyr-Hex-dicyanate

Guidance literature:: Multi-step reaction with 2 steps

1: carbodiimide

2: 78 percent / ethyl acetate / -10 - 10 °C

With carbodiimide; In ethyl acetate;
DOI:10.1021/ja00237a030

Reference yield:

: 60-18-4,18875-48-4,25619-78-7,30704-25-7
L-tyrosine

: 104549-44-2,106755-33-3
Z-Tyr-Tyr-Hex-dicyanate

Guidance literature:: Multi-step reaction with 3 steps

1: 94 percent / SOCl₂ / 12 h / 70 °C

2: carbodiimide

3: 78 percent / ethyl acetate / -10 - 10 °C

With thionyl chloride; carbodiimide; In ethyl acetate;
DOI:10.1021/ja00237a030