Boc-glu(obzl)-oh dcha

Base Information

Chemical Name:Boc-glu(obzl)-oh dcha
CAS No.:13574-84-0
Molecular Formula:C17H23NO6
Molecular Weight:518.694
Hs Code.:29224985
European Community (EC) Number:237-008-0
Mol file:13574-84-0.mol

Synonyms:13574-84-0;Boc-glu(obzl)-oh dcha;Boc-Glu(OBzl)-OH (dicyclohexylammonium) salt;Dicyclohexylamine (S)-5-(benzyloxy)-2-((tert-butoxycarbonyl)amino)-5-oxopentanoate;N-cyclohexylcyclohexanamine;(2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-5-oxo-5-phenylmethoxypentanoic acid;5-Benzyl N-(tert-butoxycarbonyl)-L-2-aminoglutarate, compound withN-dicyclohexylamine (1:1);PLGYLOMCRIZGSY-ZOWNYOTGSA-N;FD21515;5-benzyl N-(tert-butoxycarbonyl)-L-2-aminoglutarate, compound with N-dicyclohexylamine (1:1);AS-49104;J-006768;5-Benzyl N-(tert-butoxycarbonyl)-L-2-aminoglutarate,compound withn-dicyclohexylamine(1:1);Dicyclohexylamine(S)-5-(benzyloxy)-2-((tert-butoxycarbonyl)amino)-5-oxopentanoate;(2S)-5-(benzyloxy)-2-{[(tert-butoxy)carbonyl]amino}-5-oxopentanoic acid

Suppliers and Price of Boc-glu(obzl)-oh dcha

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

Crysdot
Dicyclohexylamine(S)-5-(benzyloxy)-2-((tert-butoxycarbonyl)amino)-5-oxopentanoate 95+%
10g
$ 412.00

Crysdot
Dicyclohexylamine(S)-5-(benzyloxy)-2-((tert-butoxycarbonyl)amino)-5-oxopentanoate 95+%
25g
$ 741.00

Chemenu
Dicyclohexylamine(S)-5-(benzyloxy)-2-((tert-butoxycarbonyl)amino)-5-oxopentanoate 95%
25g
$ 699.00

Chemenu
Dicyclohexylamine(S)-5-(benzyloxy)-2-((tert-butoxycarbonyl)amino)-5-oxopentanoate 95%
10g
$ 389.00

Total 17 raw suppliers

Chemical Property of Boc-glu(obzl)-oh dcha

Chemical Property:

Vapor Pressure:9.49E-12mmHg at 25°C
Melting Point:140-142 °C
Boiling Point:522.6°Cat760mmHg
Flash Point:269.9°C
PSA：113.96000
Density:1.197g/cm³
LogP:6.51110
Storage Temp.:-20°C
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:12
Exact Mass:518.33558719
Heavy Atom Count:37
Complexity:553

Purity/Quality:

98%,99%, ^*data from raw suppliers

Dicyclohexylamine(S)-5-(benzyloxy)-2-((tert-butoxycarbonyl)amino)-5-oxopentanoate 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:
Safety Statements: 22-24/25

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C)OC(=O)NC(CCC(=O)OCC1=CC=CC=C1)C(=O)O.C1CCC(CC1)NC2CCCCC2
Isomeric SMILES:CC(C)(C)OC(=O)N[C@@H](CCC(=O)OCC1=CC=CC=C1)C(=O)O.C1CCC(CC1)NC2CCCCC2

Technology Process of Boc-glu(obzl)-oh dcha

There total 5 articles about Boc-glu(obzl)-oh dcha 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: 92.0%

: 42726-92-1
Boc-Glu(OBn)-ONbn

: 13574-84-0
dicyclohexylamine salt of γ-benzyl Boc-glutamate

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; Ambient temperature;
DOI:10.1021/jo00018a052

Reference yield:

: 56-86-0,21675-62-7,23009-64-5,25104-13-6,84960-48-5,25513-46-6
L-glutamic acid

: 13574-84-0
dicyclohexylamine salt of γ-benzyl Boc-glutamate

Guidance literature:: Multi-step reaction with 2 steps

1: 59 percent / 98percent H₂SO₄ / diethyl ether / 20 h / Ambient temperature

2: 1.) Et₃N / 1.) ethyl acetate, 3 h, 2.) ethyl acetate

With sulfuric acid; triethylamine; In diethyl ether;

Reference yield:

: 100-51-6,185532-71-2
benzyl alcohol

: 13574-84-0
dicyclohexylamine salt of γ-benzyl Boc-glutamate

Guidance literature:: Multi-step reaction with 2 steps

1: 59 percent / 98percent H₂SO₄ / diethyl ether / 20 h / Ambient temperature

2: 1.) Et₃N / 1.) ethyl acetate, 3 h, 2.) ethyl acetate

With sulfuric acid; triethylamine; In diethyl ether;