D-Phenylalanine, N-acetyl-2-methoxy-

Base Information

Chemical Name:D-Phenylalanine, N-acetyl-2-methoxy-
CAS No.:193546-30-4
Molecular Formula:C12H15NO4
Molecular Weight:237.255
Hs Code.:
DSSTox Substance ID:DTXSID80444069
Nikkaji Number:J1.046.009C
Wikidata:Q82262078
Mol file:193546-30-4.mol

Synonyms:D-Phenylalanine, N-acetyl-2-methoxy-;193546-30-4;DTXSID80444069;N-Acetyl-2-methoxy-D-phenylalanine

Suppliers and Price of D-Phenylalanine, N-acetyl-2-methoxy-

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of D-Phenylalanine, N-acetyl-2-methoxy-

Chemical Property:

XLogP3:1.1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:5
Exact Mass:237.10010796
Heavy Atom Count:17
Complexity:280

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)NC(CC1=CC=CC=C1OC)C(=O)O
Isomeric SMILES:CC(=O)N[C@H](CC1=CC=CC=C1OC)C(=O)O

Technology Process of D-Phenylalanine, N-acetyl-2-methoxy-

There total 5 articles about D-Phenylalanine, N-acetyl-2-methoxy- 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:

: 52289-93-7
o-Methoxybenzyl bromide

: 193546-30-4
D-N-acetyl-2-methoxyphenylalanine

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) NaOEt / 1.) EtOH, 2.) EtOH, 3 h

2: 94 percent / aq. NaOH / 6 h / Heating

With sodium hydroxide; sodium ethanolate;
DOI:10.1002/jhet.5570340321

Reference yield:

: (Z)-2-Acetylamino-3-(2-methoxy-phenyl)-acrylic acid

: N-acetyl-(S)-2-methoxyphenylalanine

: 193546-30-4
D-N-acetyl-2-methoxyphenylalanine

Guidance literature:: With 1,2,5,6-di-isopropylidene-3,4-bis(diphenylphosphino)-D-mannitol Rh complex*BF₄; hydrogen; In acetone; at 25 ℃; for 0.25h; under 25857.4 Torr;
DOI:10.1016/S0040-4039(98)02457-5

Reference yield:

: 612-16-8
(2-methoxyphenyl)methanol

: 193546-30-4
D-N-acetyl-2-methoxyphenylalanine

Guidance literature:: Multi-step reaction with 4 steps

1: 80 percent / PBr₃ / toluene / 0.17 h / 100 °C

2: 1.) NaOEt / 1.) EtOH, 2.) EtOH, 3 h

3: 94 percent / aq. NaOH / 6 h / Heating

With sodium hydroxide; sodium ethanolate; phosphorus tribromide; In toluene;
DOI:10.1002/jhet.5570340321