Boc-pyr-oet

Base Information Edit

Chemical Name:Boc-pyr-oet
CAS No.:144978-12-1
Molecular Formula:C₁₂H₁₉NO₅
Molecular Weight:257.287
Hs Code.:2933790090
European Community (EC) Number:480-250-9,604-450-4
DSSTox Substance ID:DTXSID80420126
Nikkaji Number:J651.353K
Wikidata:Q72450610
Mol file:144978-12-1.mol

Synonyms:boc-pyr-oet;144978-12-1;(s)-ethyl-n-boc-pyroglutamate;N-Boc-L-pyroglutamic acid ethyl ester;1-Boc-L-Pyroglutamic acid ethyl ester;(S)-1-TERT-BUTYL 2-ETHYL 5-OXOPYRROLIDINE-1,2-DICARBOXYLATE;Boc-L-Pyroglutamic acid ethyl ester;Ethyl N-Boc-L-pyroglutamate;1-O-tert-butyl 2-O-ethyl (2S)-5-oxopyrrolidine-1,2-dicarboxylate;MFCD07778090;Ethyl Boc-L-pyroglutamate;SCHEMBL903617;UPCMLD00WCRH2-043;ethyl-N-Boc-(S)-pyroglutamate;N-Boc-L-pyroglutamic Acid Ethyl;DTXSID80420126;YWWWGFSJHCFVOW-QMMMGPOBSA-N;1-(tert-butyl) 2-ethyl (S)-5-oxopyrrolidine-1,2-dicarboxylate;BCP22979;CS-D1526;UPCMLD00WCRH2-043:002;AKOS015909984;AKOS015923037;N-Boc- L-pyroglutamic acid ethyl ester;AC-23796;AS-13324;(s)-ethyl n-tert-butoxycarbonylpyroglutamate;E1135;Ethyl N-(tert-Butoxycarbonyl)-L-pyroglutamate;ethyl-(2s)-n-(t-butoxycarbonyl)pyroglutamate;N-Butoxycarbonyl-5-oxo-L-proline ethyl ester;EC 480-250-9;N-tert-Butoxycarbonylpyroglutamic acid ethyl ester;Q-101864;1-(tert-Butoxycarbonyl)-5-oxo-L-proline ethyl ester;ETHYL (S)-N-(TERT-BUTOXYCARBONYL)PYROGLUTAMATE;N-(tert-Butoxycarbonyl)-L-pyroglutamic Acid Ethyl Ester;(S)-N-alpha-t-Butyloxycarbonyl-pyroglutamic acid ethyl ester;ethyl (S)-1-tert-butoxycarbonyl-2-pyrrolidone-5-carboxylate;Ethyl (S)-1-(tert-Butoxycarbonyl)-5-oxopyrrolidine-2-carboxylate;(S)-1-(tert-Butoxycarbonyl)-5-oxopyrrolidine-2-carboxylic Acid Ethyl Ester;1-TERT-BUTYL 2-ETHYL (2S)-5-OXOPYRROLIDINE-1,2-DICARBOXYLATE;2-Ethyl 1-(2-methyl-2-propanyl) (2S)-5-oxo-1,2-pyrrolidinedicarboxylate;(2S)-1-(tert-Butoxycarbonyl)-5-oxopyrrolidine-2-carboxylic acid ethyl ester;(S)-5-OXO-PYRROLIDINE-1,2-DICARBOXYLIC ACID 1-TERT-BUTYL ESTER 2-ETHYL ESTER

Suppliers and Price of Boc-pyr-oet

Supply Marketing:Edit

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
N-tert-ButoxycarbonylpyroglutamicAcidEthylEster
50g
$ 745.00

TCI Chemical
Ethyl N-(tert-Butoxycarbonyl)-L-pyroglutamate >97.0%(HPLC)(N)
1g
$ 13.00

TCI Chemical
Ethyl N-(tert-Butoxycarbonyl)-L-pyroglutamate >97.0%(HPLC)(N)
5g
$ 38.00

Medical Isotopes, Inc.
(S)-Ethyl-N-Boc-pyroglutamate 95+%
100 g
$ 595.00

Matrix Scientific
(S)-1-tert-Butyl 2-ethyl 5-oxopyrrolidine-1,2-dicarboxylate 95%
25g
$ 367.00

Matrix Scientific
(S)-1-tert-Butyl 2-ethyl 5-oxopyrrolidine-1,2-dicarboxylate 95%
100g
$ 1046.00

Labseeker
N-Boc-L-pyroglutamicacidethylester 95
5kg
$ 1500.00

Crysdot
(S)-Ethyl-N-Boc-pyroglutamate 97%
100g
$ 158.00

Chemenu
1-tert-butyl2-ethyl(2S)-5-oxopyrrolidine-1,2-dicarboxylate 97%
100g
$ 143.00

Biosynth Carbosynth
N-Boc-L-pyroglutamic acid etHyl ester
500 g
$ 300.00

Total 151 raw suppliers

Chemical Property of Boc-pyr-oet Edit

Chemical Property:

Appearance/Colour:White crystalline powder
Vapor Pressure:8.03E-06mmHg at 25°C
Melting Point:52.0 to 56.0 °C
Refractive Index:1.486
Boiling Point:375 °C at 760 mmHg
PKA:-4.15±0.40(Predicted)
Flash Point:180.6 °C
PSA：72.91000
Density:1.182 g/cm³
LogP:1.41350
Storage Temp.:Keep in dark place,Sealed in dry,Room Temperature
Solubility.:soluble in Methanol
XLogP3:1.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:5
Exact Mass:257.12632271
Heavy Atom Count:18
Complexity:358

Purity/Quality:

99% ^*data from raw suppliers

N-tert-ButoxycarbonylpyroglutamicAcidEthylEster ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC(=O)C1CCC(=O)N1C(=O)OC(C)(C)C
Isomeric SMILES:CCOC(=O)[C@@H]1CCC(=O)N1C(=O)OC(C)(C)C
Uses N-tert-Butoxycarbonylpyroglutamic Acid Ethyl Ester is a compound derived from pyroglutamic acid, used in the synthesis of various pharmacological compounds. It is used in the synthesis of HCV protesase inhibitors as well as alkyl renin inhibitors.

Technology Process of Boc-pyr-oet

There total 15 articles about Boc-pyr-oet 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: 100.0%