bis(2,2,2-trifluoroethyl) (1-amino-2-phenylethyl)phosphonate hydrobromide

Base Information

Chemical Name:bis(2,2,2-trifluoroethyl) (1-amino-2-phenylethyl)phosphonate hydrobromide
CAS No.:1423779-12-7
Molecular Formula:BrH*C₁₂H₁₄F₆NO₃P
Molecular Weight:446.124
Hs Code.:

Synonyms:bis(2,2,2-trifluoroethyl) (1-amino-2-phenylethyl)phosphonate hydrobromide

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

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Chemical Property of bis(2,2,2-trifluoroethyl) (1-amino-2-phenylethyl)phosphonate hydrobromide

Chemical Property:

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Technology Process of bis(2,2,2-trifluoroethyl) (1-amino-2-phenylethyl)phosphonate hydrobromide

There total 1 articles about bis(2,2,2-trifluoroethyl) (1-amino-2-phenylethyl)phosphonate hydrobromide 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:

: 174298-12-5
benzyl N-{1-[bis(2,2,2-trifluoroethoxy)phosphoryl]-2-phenylethyl}carbamate

: 1423779-12-7
bis(2,2,2-trifluoroethyl) (1-amino-2-phenylethyl)phosphonate hydrobromide

Guidance literature:: With hydrogen bromide; acetic acid;
DOI:10.1016/j.tetlet.2013.01.039

Reference yield:

: 1423779-12-7
bis(2,2,2-trifluoroethyl) (1-amino-2-phenylethyl)phosphonate hydrobromide

: 23361-28-6
N-(tert-butyloxycarbonyl)-L-valyl-L-proline

: 1423779-06-9
tert-butyl N-{(2S)-1-[(2S)-2-({1-[bis(2,2,2-trifluoroethoxy)phosphoryl]-2-phenylethyl}carbamoyl)pyrrolidin-1-yl]-3-methyl-1-oxobutan-2-yl}carbamate

Guidance literature:: With O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; In acetonitrile; at 20 ℃; for 24h; Optical yield = 2 %de;
DOI:10.1016/j.tetlet.2013.01.039