Z-Ile-pro-OH

Base Information

Chemical Name:Z-Ile-pro-OH
CAS No.:13211-37-5
Molecular Formula:C19H26 N2 O5
Molecular Weight:362.42
Hs Code.:
Mol file:13211-37-5.mol

Synonyms:Z-ILE-PRO-OH;13211-37-5;Cbz-Ile-Pro-OH;(S)-1-((2S,3S)-2-(((Benzyloxy)carbonyl)amino)-3-methylpentanoyl)pyrrolidine-2-carboxylic acid;N-Benzyloxycarbonyl-L-isoleucyl-L-proline;N-cbz-l-isoleucyl-l-proline;SCHEMBL8331221;(2S)-1-[(2S,3S)-2-{[(BENZYLOXY)CARBONYL]AMINO}-3-METHYLPENTANOYL]PYRROLIDINE-2-CARBOXYLIC ACID;HY-P5024;MFCD00037330;CS-0675692;(S)-1-((2S,3S)-2-(benzyloxycarbonylamino)-3-methylpentanoyl)pyrrolidine-2-carboxylic acid

Suppliers and Price of Z-Ile-pro-OH

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

TRC
Z-Ile-Pro-OH
500mg
$ 285.00

American Custom Chemicals Corporation
N-BENZYLOXYCARBONYL-L-ISOLEUCYL-L-PROLINE 99.00%
5G
$ 1582.35

Total 14 raw suppliers

Chemical Property of Z-Ile-pro-OH

Chemical Property:

Vapor Pressure:1.06E-14mmHg at 25°C
Boiling Point:588.7°Cat760mmHg
PKA:3.52±0.20(Predicted)
Flash Point:309.8°C
PSA：95.94000
Density:1.224g/cm³
LogP:2.73190
Storage Temp.:−20°C
XLogP3:2.6
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:8
Exact Mass:362.18417193
Heavy Atom Count:26
Complexity:504

Purity/Quality:

99% ^*data from raw suppliers

Z-Ile-Pro-OH ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCC(C)C(C(=O)N1CCCC1C(=O)O)NC(=O)OCC2=CC=CC=C2
Isomeric SMILES:CC[C@H](C)[C@@H](C(=O)N1CCC[C@H]1C(=O)O)NC(=O)OCC2=CC=CC=C2

Technology Process of Z-Ile-pro-OH

There total 4 articles about Z-Ile-pro-OH 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: 82.0%

: 3391-99-9
N-Z-L-isoleucine N-hydroxysuccinimide ester

: 147-85-3,25191-13-3,37159-97-0,4305-67-3,4607-28-7
L-proline

: 13211-37-5
Z-Ile-Pro-OH

Guidance literature:: With TEA; In N,N-dimethyl-formamide; for 72h; Ambient temperature;
DOI:10.1016/S0040-4020(01)98916-1

Reference yield: 82.0%

: 40290-70-8
Z-Ile-Pro-OCH₃

: 13211-37-5
Z-Ile-Pro-OH

Guidance literature:: With sodium hydroxide;

Reference yield:

: 2577-48-2
methyl (2S)-pyrrolidine carboxylate

: 13211-37-5
Z-Ile-Pro-OH

Guidance literature:: Multi-step reaction with 2 steps

1: 82 percent / dicyclohexylcarbodiimide

2: 82 percent / NaOH

With sodium hydroxide; dicyclohexyl-carbodiimide;