XJ735

Base Information

Chemical Name:XJ735
CAS No.:153381-95-4
Molecular Formula:C₂₃H₃₂N₈O₇
Molecular Weight:532.556
Hs Code.:
Mol file:153381-95-4.mol

Synonyms:L-Asparticacid, N-[3-(aminomethyl)benzoyl]-L-alanyl-L-arginylglycyl-, cyclic (41®1)-peptide;3,6,9,12,15-Pentaazabicyclo[15.3.1]heneicosane, cyclic peptide deriv.; 2: PN:US6056958 SEQID: 2 claimed protein; XJ 735

Suppliers and Price of XJ735

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Sigma-Aldrich
Cyclo(Ala-Arg-Gly-Asp-3-Aminomethylbenzoyl) ≥96% (HPLC)
1mg
$ 368.00

American Custom Chemicals Corporation
CYCLO(ALA-ARG-GLY-ASP-3-AMINOMETHYLBENZOYL)TRIFLUOROACETATE SALT 95.00%
50MG
$ 1904.02

American Custom Chemicals Corporation
CYCLO(ALA-ARG-GLY-ASP-3-AMINOMETHYLBENZOYL)TRIFLUOROACETATE SALT 95.00%
5MG
$ 749.60

Total 7 raw suppliers

Chemical Property of XJ735

Chemical Property:

PKA:4.02±0.10(Predicted)
PSA：282.00000
Density:1.53±0.1 g/cm3(Predicted)
LogP:0.72670
Storage Temp.:−20°C

Purity/Quality:

98%,99%, ^*data from raw suppliers

Cyclo(Ala-Arg-Gly-Asp-3-Aminomethylbenzoyl) ≥96% (HPLC) ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:
Safety Statements: 22-24/25

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of XJ735

There total 6 articles about XJ735 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:

: 1877-72-1
3-Cyanobenzoic acid

: 153381-95-4
cyclo(D-Ala-Arg-Gly-Asp-Mamb)

Guidance literature:: Multi-step reaction with 3 steps

1: 64 percent / H₂, conc. HCl / 10percent Pd/C / ethanol / 38 h

2: 64 percent / Et₃N / H₂O / Ambient temperature

3: solid-phase synthesis using p-nitrobenzophenone oxime solid resin

With hydrogenchloride; hydrogen; triethylamine; palladium on activated charcoal; In ethanol; water;
DOI:10.1021/ja00087a007

Reference yield:

: 1877-72-1
3-Cyanobenzoic acid

: 153381-95-4
cyclo(Ala-Arg-Gly-Asp-Mamb)

Guidance literature:: Multi-step reaction with 3 steps

1: 64 percent / H₂, conc. HCl / 10percent Pd/C / ethanol / 38 h

2: 64 percent / Et₃N / H₂O / Ambient temperature

3: solid-phase synthesis using p-nitrobenzophenone oxime solid resin

With hydrogenchloride; hydrogen; triethylamine; palladium on activated charcoal; In ethanol; water;
DOI:10.1021/ja00087a007

Reference yield:

: 876-03-9
3-(aminomethyl)benzoic acid hydrochloride

: 153381-95-4
cyclo(D-Ala-Arg-Gly-Asp-Mamb)

Guidance literature:: Multi-step reaction with 2 steps

1: 64 percent / Et₃N / H₂O / Ambient temperature

2: solid-phase synthesis using p-nitrobenzophenone oxime solid resin

With triethylamine; In water;
DOI:10.1021/ja00087a007