(S)-Methyl 2-((tert-butoxycarbonyl)amino)-3-(4-iodophenyl)propanoate

Base Information

Chemical Name:(S)-Methyl 2-((tert-butoxycarbonyl)amino)-3-(4-iodophenyl)propanoate
CAS No.:796072-33-8
Molecular Formula:C15H20INO4
Molecular Weight:405.233
Hs Code.:
UNII:T2G0WI9NEZ

Synonyms:796072-33-8;N-Boc-4-iodo-DL-phenylalanine methyl ester;T2G0WI9NEZ;(+/-)-(R/S)-2-tert-Butoxycarbonylamino-3-(4-iodo-phenyl)-propionic acid methyl ester;(S)-Methyl 2-((tert-butoxycarbonyl)amino)-3-(4-iodophenyl)propanoate;D,L-phenylalanine, N-((1,1-dimethylethoxy)carbonyl)-4-iodo-, methyl ester;METHYL 2-((TERT-BUTOXYCARBONYL)AMINO)-3-(4-IODOPHENYL)PROPANOATE;MFCD07366813;boc-4-iodo-l-phenylalanine methyl ester;UNII-T2G0WI9NEZ;SCHEMBL1133286;HNCUXLSIVYDGBW-UHFFFAOYSA-N;AT18500;N-Boc-4-iodo-DL-phenylalaninemethylester;N-t-boc-4-iodophenylalanine methyl ester;SY245134;CS-0455873;2-tert-Butoxycarbonylamino-3-(4-iodophenyl)-propanoic acid methyl ester

Suppliers and Price of (S)-Methyl 2-((tert-butoxycarbonyl)amino)-3-(4-iodophenyl)propanoate

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Activate Scientific
N-Boc-4-iodo-DL-phenylalanine methyl ester 95%
5 g
$ 573.00

Activate Scientific
N-Boc-4-iodo-DL-phenylalanine methyl ester 95%
1 g
$ 178.00

Acrotein
N-Boc-4-iodo-DL-phenylalaninemethylester 97%
0.5g
$ 91.67

Total 6 raw suppliers

Chemical Property of (S)-Methyl 2-((tert-butoxycarbonyl)amino)-3-(4-iodophenyl)propanoate

Chemical Property:

PSA：64.63000
LogP:3.29090
XLogP3:3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:7
Exact Mass:405.04371
Heavy Atom Count:21
Complexity:359

Purity/Quality:

99% ^*data from raw suppliers

N-Boc-4-iodo-DL-phenylalanine methyl ester 95% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C)OC(=O)NC(CC1=CC=C(C=C1)I)C(=O)OC

Technology Process of (S)-Methyl 2-((tert-butoxycarbonyl)amino)-3-(4-iodophenyl)propanoate

There total 5 articles about (S)-Methyl 2-((tert-butoxycarbonyl)amino)-3-(4-iodophenyl)propanoate 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: 98.0%

: 74-88-4
methyl iodide

: 796072-33-8,210962-91-7
N-tert-butyloxycarbonyl-(L)4-iodophenylalanine methyl ester

Guidance literature:: N-Boc-DL-4-iodophenylalanine; With potassium carbonate; In N,N-dimethyl-formamide; for 0.25h;

methyl iodide; In N,N-dimethyl-formamide; at 0 - 20 ℃; for 16h;

Reference yield: 98.0%

: 103882-09-3
N-Boc-DL-4-iodophenylalanine

: 74-88-4
methyl iodide

: 796072-33-8,210962-91-7
N-tert-butyloxycarbonyl-(L)4-iodophenylalanine methyl ester

Guidance literature:: With potassium carbonate; In DMF (N,N-dimethyl-formamide); at 20 ℃; for 16h;

Reference yield: 81.0%

: methyl 3-(4-((trifluoromethyl)sulfonyloxy)phenyl)-2-((tert-butoxy)carbonylamino)propionate

: 796072-33-8,210962-91-7
N-tert-butyloxycarbonyl-(L)4-iodophenylalanine methyl ester

Guidance literature:: With iodine; lithium fluoride; sodium iodide; In acetonitrile; at 25 ℃; for 24h; Inert atmosphere; UV-irradiation; Schlenk technique;
DOI:10.1021/jacs.7b03538