Ethyl 2-[(tert-butoxycarbonyl)amino]-1,3-oxazole-5-carboxylate

Base Information

Chemical Name:Ethyl 2-[(tert-butoxycarbonyl)amino]-1,3-oxazole-5-carboxylate
CAS No.:244236-51-9
Molecular Formula:C₁₁H₁₆N₂O₅
Molecular Weight:256.258
Hs Code.:
Mol file:244236-51-9.mol

Synonyms:2-tert-butoxycarbonylamino-oxazole-4-carboxylic acid ethyl ester

Suppliers and Price of Ethyl 2-[(tert-butoxycarbonyl)amino]-1,3-oxazole-5-carboxylate

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

Ambeed
4-Oxazolecarboxylicacid,2-[[(1,1-dimethylethoxy)carbonyl]amino]-,ethylester 95%
250mg
$ 82.00

Ambeed
4-Oxazolecarboxylicacid,2-[[(1,1-dimethylethoxy)carbonyl]amino]-,ethylester 95%
100mg
$ 45.00

Ambeed
4-Oxazolecarboxylicacid,2-[[(1,1-dimethylethoxy)carbonyl]amino]-,ethylester 95%
1g
$ 208.00

AK Scientific
2-N-bocaminooxazole-4-carboxylicacidethylester
5g
$ 937.00

Advanced Chemicals Intermediatesced Chemicals Intermediates
2-tert-Butoxycarbonylamino-oxazole-4-carboxylicacidethylester 95%+
500mg
$ 181.25

Acints
2-tert-Butoxycarbonylamino-oxazole-4-carboxylicacidethylester 95%+
500mg
$ 181.25

Total 3 raw suppliers

Chemical Property of Ethyl 2-[(tert-butoxycarbonyl)amino]-1,3-oxazole-5-carboxylate

Chemical Property:

Storage Temp.:2-8°C

Purity/Quality:

97% ^*data from raw suppliers

4-Oxazolecarboxylicacid,2-[[(1,1-dimethylethoxy)carbonyl]amino]-,ethylester 95% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:Xi

MSDS Files:

Useful:

Technology Process of Ethyl 2-[(tert-butoxycarbonyl)amino]-1,3-oxazole-5-carboxylate

There total 6 articles about Ethyl 2-[(tert-butoxycarbonyl)amino]-1,3-oxazole-5-carboxylate 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: 60.0%

: 24424-99-5
di-tert-butyl dicarbonate

: 177760-52-0
ethyl 2-aminooxazole-4-carboxylate

: 244236-51-9
2-tert-butoxycarbonylamino-oxazole-4-carboxylic acid ethyl ester

Guidance literature:: With dmap; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 40 ℃;

Reference yield:

: 24424-99-5
di-tert-butyl dicarbonate

: 177760-52-0
ethyl 2-aminooxazole-4-carboxylate

: 244236-51-9
2-tert-butoxycarbonylamino-oxazole-4-carboxylic acid ethyl ester

: 566206-02-8
ethyl 2-(N,N-bis-Boc)amino-4-oxazolecarboxylate

Guidance literature:: With dmap; In dichloromethane; at 20 ℃; for 20h;

Reference yield:

: 177760-52-0
ethyl 2-aminooxazole-4-carboxylate

: 244236-51-9
2-tert-butoxycarbonylamino-oxazole-4-carboxylic acid ethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: Et₃N; DMAP / tetrahydrofuran / 20 °C

2: TFA

With dmap; triethylamine; trifluoroacetic acid; In tetrahydrofuran; 1: Substitution / 2: Substitution;
DOI:10.1055/s-1999-2819