4-(Benzylsulfanyl)-L-phenylalanine

Base Information

Chemical Name:4-(Benzylsulfanyl)-L-phenylalanine
CAS No.:88170-98-3
Molecular Formula:C16H17NO2S
Molecular Weight:287.382
Hs Code.:
DSSTox Substance ID:DTXSID20570290
Wikidata:Q82457680

Synonyms:4-(Benzylsulfanyl)-L-phenylalanine;88170-98-3;DTXSID20570290;EN300-43381874;(2S)-2-amino-3-[4-(benzylsulfanyl)phenyl]propanoic acid

Suppliers and Price of 4-(Benzylsulfanyl)-L-phenylalanine

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 4-(Benzylsulfanyl)-L-phenylalanine

Chemical Property:

XLogP3:0.5
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:6
Exact Mass:287.09799996
Heavy Atom Count:20
Complexity:297

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)CSC2=CC=C(C=C2)CC(C(=O)O)N
Isomeric SMILES:C1=CC=C(C=C1)CSC2=CC=C(C=C2)C[C@@H](C(=O)O)N

Technology Process of 4-(Benzylsulfanyl)-L-phenylalanine

There total 2 articles about 4-(Benzylsulfanyl)-L-phenylalanine 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:

: 84053-10-1
4-mercapto-L-phenylalanine

: 100-39-0
benzyl bromide

: 88170-98-3
L-S-benzyl-4'-mercaptophenylalanine

Guidance literature:: With triethylamine; In ethanol; for 15h; Yield given; Ambient temperature;
DOI:10.1002/hlca.19830660504

Reference yield:

: 63-91-2,25191-15-5,658-69-5,67675-33-6
L-phenylalanine

: 88170-98-3
L-S-benzyl-4'-mercaptophenylalanine

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) chlorosulfonic acid; 2.) conc. HCl, Sn / 1.) -15 deg C, 4 h; 2.) reflux, 2 h

2: Et₃N / ethanol / 15 h / Ambient temperature

With hydrogenchloride; chlorosulfonic acid; tin; triethylamine; In ethanol;
DOI:10.1002/hlca.19830660504