AMINO ACID HYDROXAMATES DL-PHENYLALANINE HYDROXAMATE

Base Information

Chemical Name:AMINO ACID HYDROXAMATES DL-PHENYLALANINE HYDROXAMATE
CAS No.:36207-44-0
Molecular Formula:C9H12 N2 O2
Molecular Weight:180.206
Hs Code.:2924299090
Mol file:36207-44-0.mol

Synonyms:Benzenepropanamide,a-amino-N-hydroxy-, (?à)-; DL-Phenylalanine hydroxamicacid

Suppliers and Price of AMINO ACID HYDROXAMATES DL-PHENYLALANINE HYDROXAMATE

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

American Custom Chemicals Corporation
AMINO ACID HYDROXAMATES-DL-PHENYLALANINE HYDROXAMATE 95.00%
5MG
$ 496.68

Total 3 raw suppliers

Chemical Property of AMINO ACID HYDROXAMATES DL-PHENYLALANINE HYDROXAMATE

Chemical Property:

PKA:10.11±0.40(Predicted)
PSA：78.84000
Density:1.232±0.06 g/cm3(Predicted)
LogP:1.60240
Storage Temp.:−20°C

Purity/Quality:

99% ^*data from raw suppliers

AMINO ACID HYDROXAMATES-DL-PHENYLALANINE HYDROXAMATE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s): Xi
Hazard Codes:Xi
Statements: 36/37/38
Safety Statements: 26

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of AMINO ACID HYDROXAMATES DL-PHENYLALANINE HYDROXAMATE

There total 10 articles about AMINO ACID HYDROXAMATES DL-PHENYLALANINE HYDROXAMATE 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: 85.0%

: 7524-50-7
methyl (2S)-2-amino-3-phenylpropanoate hydrochloride

: 5703-58-2,36207-44-0,134235-84-0,19254-08-1
L-Phenylalanine hydroxamate

Guidance literature:: methyl (2S)-2-amino-3-phenylpropanoate hydrochloride; With potassium hydroxide; In methanol; for 0.166667h; Cooling with ice;

With hydroxylamine; In methanol; at 20 ℃; Inert atmosphere;
DOI:10.1021/ic202347j

Reference yield:

: 3081-24-1
H-Phe-OEt

: 5703-58-2,36207-44-0,134235-84-0,19254-08-1
L-Phenylalanine hydroxamate

Guidance literature:: With hydroxylamine; In dimethyl sulfoxide; at 40 ℃; for 1h; Kinetics; protease I of Streptomyces griseus in 0.1 M phosphate buffer; other conc. of DMSO and NH₂OH, different times: Activation of transfer reaction by organic solvents;

Reference yield:

: 35661-40-6
N-Fmoc L-Phe

: 5703-58-2,36207-44-0,134235-84-0,19254-08-1
L-Phenylalanine hydroxamate

Guidance literature:: N-Fmoc L-Phe; With 4-methyl-morpholine; hydroxylamine Wang resin; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; In N,N-dimethyl-formamide; for 0.5h;

With piperidine; In N,N-dimethyl-formamide; for 0.166667h;

With trifluoroacetic acid; In dichloromethane; at 20 ℃; for 0.5h; Further stages.;
DOI:10.1021/jm061058c