t-butyl [(1S)-2-hydroxy-1-(4-iodobenzyl)ethyl]carbamate

Base Information

Chemical Name:t-butyl [(1S)-2-hydroxy-1-(4-iodobenzyl)ethyl]carbamate
CAS No.:210962-68-8
Molecular Formula:C₁₄H₂₀INO₃
Molecular Weight:377.222
Hs Code.:
DSSTox Substance ID:DTXSID501124929
Nikkaji Number:J2.062.796D

Synonyms:SCHEMBL6855658;t-butyl [(1S)-2-hydroxy-1-(4-iodobenzyl)ethyl]carbamate;IHPVVBDNLUZOLT-LBPRGKRZSA-N;DTXSID501124929;210962-68-8;Carbamic acid, [(1S)-2-hydroxy-1-[(4-iodophenyl)methyl]ethyl]-, 1,1-dimethylethyl ester

Suppliers and Price of t-butyl [(1S)-2-hydroxy-1-(4-iodobenzyl)ethyl]carbamate

Supply Marketing:

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

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Chemical Property of t-butyl [(1S)-2-hydroxy-1-(4-iodobenzyl)ethyl]carbamate

Chemical Property:

XLogP3:2.9
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:6
Exact Mass:377.04879
Heavy Atom Count:19
Complexity:283

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(C)(C)OC(=O)NC(CC1=CC=C(C=C1)I)CO
Isomeric SMILES:CC(C)(C)OC(=O)N[C@@H](CC1=CC=C(C=C1)I)CO

Technology Process of t-butyl [(1S)-2-hydroxy-1-(4-iodobenzyl)ethyl]carbamate

There total 2 articles about t-butyl [(1S)-2-hydroxy-1-(4-iodobenzyl)ethyl]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: 89.0%

: 103882-09-3,62129-44-6
N-Boc-4-I-Phe-OH

: 210962-68-8
(S)-N-tert-butoxycarbonyl-4-iodophenylalaninol

Guidance literature:: N-Boc-4-I-Phe-OH; With 4-methyl-morpholine; isobutyl chloroformate; In tetrahydrofuran; at -15 ℃; for 0.25h;

With sodium tetrahydroborate; In tetrahydrofuran; at -15 ℃; for 0.5h;
DOI:10.1021/jm051226l