eledoisin (6-11)

Base Information

Chemical Name:eledoisin (6-11)
CAS No.:4575-63-7
Molecular Formula:C₃₁H₅₁N₇O₆S
Molecular Weight:649.855
Hs Code.:
Mol file:4575-63-7.mol

Synonyms:(2S,3S)-2-[(S)-2-((S)-2-Amino-propionylamino)-3-phenyl-propionylamino]-3-methyl-pentanoic acid {[(S)-1-((S)-1-carbamoyl-3-methylsulfanyl-propylcarbamoyl)-3-methyl-butylcarbamoyl]-methyl}-amide;

Suppliers and Price of eledoisin (6-11)

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 eledoisin (6-11)

Chemical Property:

Melting Point:250 °C (decomp)
Boiling Point:1035.9±65.0 °C(Predicted)
PKA:13.37±0.46(Predicted)
PSA：239.91000
Density:1.175±0.06 g/cm3(Predicted)
LogP:3.31740

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of eledoisin (6-11)

There total 6 articles about eledoisin (6-11) 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:

: 21853-73-6
Boc-Ala-Phe-Ile-Gly-Leu-Met-NH₂

: 4575-63-7
L-Alanyl-L-phenylalanyl-L-isoleucyl-glycyl-L-leucyl-L-methioninamid

Guidance literature:: With trifluoroacetic acid;

Reference yield:

: 2578-84-9
N-benzyloxycarbonyl-L-phenylalanine p-nitrophenyl ester

: 4575-63-7
L-Alanyl-L-phenylalanyl-L-isoleucyl-glycyl-L-leucyl-L-methioninamid

Guidance literature:: Multi-step reaction with 4 steps

1: (i) HBr, AcOH, (ii) /BRN= 2572134/, Et₃N, DMF

2: (i) HBr, AcOH, (ii) /BRN= 1892073/, Et₃N, DMF

3: (i) aq. NaOH, EtOH, (ii) /BRN= 4164279/, DCC, Py

4: CF₃CO₂H

With trifluoroacetic acid;

Reference yield:

: 2131-00-2
leucyl-methionine amide hydrochloride

: 4575-63-7
L-Alanyl-L-phenylalanyl-L-isoleucyl-glycyl-L-leucyl-L-methioninamid

Guidance literature:: Multi-step reaction with 2 steps

1: (i) aq. NaOH, EtOH, (ii) /BRN= 4164279/, DCC, Py

2: CF₃CO₂H

With trifluoroacetic acid;