TASP0415914

Base Information

Chemical Name:TASP0415914
CAS No.:1292300-75-4
Molecular Formula:C₁₃H₁₇N₅O₃S
Molecular Weight:323.376
Hs Code.:
Mol file:1292300-75-4.mol

Synonyms:

Suppliers and Price of TASP0415914

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

Usbiological
TASP-0415914
1mg
$ 420.00

DC Chemicals
TASP0415914 >98%
250 mg
$ 1500.00

DC Chemicals
TASP0415914 >98%
100 mg
$ 800.00

DC Chemicals
TASP0415914 >98%
50 mg
$ 450.00

AK Scientific
TASP0415914
100mg
$ 2270.00

Adipogen Life Sciences
TASP0415914 ≥95%
100 mg
$ 2430.00

Adipogen Life Sciences
TASP0415914 ≥95%
5 mg
$ 313.00

Total 9 raw suppliers

Chemical Property of TASP0415914

Chemical Property:

Purity/Quality:

99%, ^*data from raw suppliers

TASP-0415914 ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of TASP0415914

There total 9 articles about TASP0415914 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:

: C₁₅H₁₉N₅O₄S

: 1292300-75-4
N-{5-[3-(3-hydroxypiperidin-1-yl)-1,2,4-oxadiazol-5-yl]-4-methyl-1,3-thiazol-2-yl}acetamide

Guidance literature:: With sodium hydroxide; In tetrahydrofuran; ethanol; at 20 ℃; for 15h;
DOI:10.1016/j.bmc.2013.10.042

Reference yield:

: 67899-00-7
2-amino-4-methyl-thiazole-5-carboxylic acid

: 1292300-75-4
N-{5-[3-(3-hydroxypiperidin-1-yl)-1,2,4-oxadiazol-5-yl]-4-methyl-1,3-thiazol-2-yl}acetamide

Guidance literature:: Multi-step reaction with 3 steps

1: pyridine / tetrahydrofuran / 21 h / 0 - 20 °C

2: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 18 h / 20 - 100 °C

3: sodium hydroxide / ethanol; tetrahydrofuran / 15 h / 20 °C

With pyridine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; sodium hydroxide; In tetrahydrofuran; ethanol; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2013.10.042

Reference yield:

: 85275-45-2
N-tert-butoxycarbonyl-3-piperidinol

: 1292300-75-4
N-{5-[3-(3-hydroxypiperidin-1-yl)-1,2,4-oxadiazol-5-yl]-4-methyl-1,3-thiazol-2-yl}acetamide

Guidance literature:: Multi-step reaction with 6 steps

1: pyridine / 4 h / 0 - 20 °C

2: hydrogenchloride / ethyl acetate / 24 h / 20 °C

3: potassium carbonate / acetonitrile / 4 h / 20 °C

4: hydroxylamine / ethanol; water / 1 h / 20 °C

5: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 18 h / 20 - 100 °C

6: sodium hydroxide / ethanol; tetrahydrofuran / 15 h / 20 °C

With pyridine; hydrogenchloride; hydroxylamine; potassium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; sodium hydroxide; In tetrahydrofuran; ethanol; water; ethyl acetate; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1016/j.bmc.2013.10.042