1,1-Dimethylethyl N-[(1S)-1-(aminocarbonyl)-3-phenylpropyl]carbamate

Base Information

Chemical Name:1,1-Dimethylethyl N-[(1S)-1-(aminocarbonyl)-3-phenylpropyl]carbamate
CAS No.:110755-51-6
Molecular Formula:C₁₅H₂₂N₂O₃
Molecular Weight:278.351
Hs Code.:
DSSTox Substance ID:DTXSID901160385
Nikkaji Number:J1.590.730D

Synonyms:SCHEMBL6802106;DTXSID901160385;110755-51-6;1,1-Dimethylethyl N-[(1S)-1-(aminocarbonyl)-3-phenylpropyl]carbamate

Suppliers and Price of 1,1-Dimethylethyl N-[(1S)-1-(aminocarbonyl)-3-phenylpropyl]carbamate

Supply Marketing:

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

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Chemical Property of 1,1-Dimethylethyl N-[(1S)-1-(aminocarbonyl)-3-phenylpropyl]carbamate

Chemical Property:

XLogP3:2.2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:7
Exact Mass:278.16304257
Heavy Atom Count:20
Complexity:331

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(C)(C)OC(=O)NC(CCC1=CC=CC=C1)C(=O)N
Isomeric SMILES:CC(C)(C)OC(=O)N[C@@H](CCC1=CC=CC=C1)C(=O)N

Technology Process of 1,1-Dimethylethyl N-[(1S)-1-(aminocarbonyl)-3-phenylpropyl]carbamate

There total 9 articles about 1,1-Dimethylethyl N-[(1S)-1-(aminocarbonyl)-3-phenylpropyl]carbamate 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%

: C₂₀H₂₉NO₆

: 110755-51-6
L-N-Boc-homophenylalanine amide

Guidance literature:: With ammonia; In water; at -10 - 20 ℃; for 4.5h;

Reference yield: 90.0%

: 82732-07-8,108524-68-1,142926-43-0,100564-78-1
Boc-L-homophenylalanine

: 110755-51-6
L-N-Boc-homophenylalanine amide

Guidance literature:: Boc-L-homophenylalanine; With benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; In N,N-dimethyl-formamide; for 0.333333h;

With ammonium hydroxide; In N,N-dimethyl-formamide; for 16h; Further stages.;
DOI:10.1021/jm020209i

Reference yield: 59.9%

: 1335290-25-9
DL-N-Boc-homoPhe-SEt

: 110755-51-6
L-N-Boc-homophenylalanine amide

Guidance literature:: With ammonia; 1,8-diazabicyclo[5.4.0]undec-7-ene; In tert-butyl alcohol; at 37 ℃; for 30h; optical yield given as %ee; Resolution of racemate; Enzymatic reaction;
DOI:10.1002/adsc.201100389