H-ASP-PHE-NH2

Base Information

Chemical Name:H-ASP-PHE-NH2
CAS No.:5241-71-4
Molecular Formula:C13H17N3O4
Molecular Weight:279.296
Hs Code.:
Mol file:5241-71-4.mol

Synonyms:L-α-Aspartyl-L-phenylalaninamide;

Suppliers and Price of H-ASP-PHE-NH2

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

Biosynth Carbosynth
H-Asp-Phe-NH2
500 mg
$ 300.00

Biosynth Carbosynth
H-Asp-Phe-NH2
250 mg
$ 175.00

Biosynth Carbosynth
H-Asp-Phe-NH2
1 g
$ 525.00

American Custom Chemicals Corporation
L-ASPARTIC ACID-L-PHENYLALANINE AMIDE 98.00%
5G
$ 1934.63

American Custom Chemicals Corporation
L-ASPARTIC ACID-L-PHENYLALANINE AMIDE 98.00%
1G
$ 1149.23

AK Scientific
H-Asp-phe-NH2
500mg
$ 455.00

Total 18 raw suppliers

Chemical Property of H-ASP-PHE-NH2

Chemical Property:

Boiling Point:647 °C at 760 mmHg
Flash Point:345.1 °C
PSA：135.51000
Density:1.326 g/cm³
LogP:0.79270
Storage Temp.:-15°C

Purity/Quality:

99% ^*data from raw suppliers

H-Asp-Phe-NH2 ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of H-ASP-PHE-NH2

There total 11 articles about H-ASP-PHE-NH2 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: 100.0%

: 110575-50-3
(S)-3-tert-Butoxycarbonylamino-N-((S)-1-carbamoyl-2-phenyl-ethyl)-succinamic acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester

: 5241-71-4
Asp-Phe-NH₂

Guidance literature:: With trifluorormethanesulfonic acid; methyl-phenyl-thioether; diphenyl sulfide; In trifluoroacetic acid; at 0 ℃; for 2h;