FGH-10019

Base Information

Chemical Name:FGH-10019
CAS No.:1046045-61-7
Molecular Formula:C18H19N3O2S2
Molecular Weight:373.5
Hs Code.:
Mol file:1046045-61-7.mol

Synonyms:N-(4-(2-(2-propylpyridin-4-yl)thiazol-4-yl)phenyl)methanesulfonamide;

Suppliers and Price of FGH-10019

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

DC Chemicals
FGH10019 >98%
1 g
$ 2600.00

DC Chemicals
FGH10019 >98%
250 mg
$ 1300.00

DC Chemicals
FGH10019 >98%
100 mg
$ 750.00

Crysdot
FGH10019 98+%
5mg
$ 243.00

Crysdot
FGH10019 98+%
10mg
$ 347.00

Crysdot
FGH10019 98+%
50mg
$ 1042.00

Crysdot
FGH10019 98+%
100mg
$ 1459.00

ChemScene
FGH10019 99.43%
50mg
$ 1440.00

ChemScene
FGH10019 99.43%
10mg
$ 480.00

ChemScene
FGH10019 99.43%
5mg
$ 330.00

Total 9 raw suppliers

Chemical Property of FGH-10019

Chemical Property:

Boiling Point:578.4±60.0 °C(Predicted)
PKA:7.16±0.10(Predicted)
PSA：108.57000
Density:1.307±0.06 g/cm3(Predicted)
LogP:5.34990

Purity/Quality:

99% ^*data from raw suppliers

FGH10019 >98% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of FGH-10019

There total 8 articles about FGH-10019 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: 87.0%

: 1046045-58-2
4-[2-(2-propylpyridin-4-yl)-1,3-thiazol-4-yl]aniline

: 124-63-0
methanesulfonyl chloride

: 1046045-61-7
N-(4-(2-(2-propylpyridin-4-yl)thiazol-4-yl)phenyl)methanesulfonamide

Guidance literature:: With pyridine; In dichloromethane; at 0 ℃; for 0.5h;
DOI:10.1021/jm200304y

Reference yield:

: 99-81-0
4-Nitrophenacyl bromide

: 1046045-61-7
N-(4-(2-(2-propylpyridin-4-yl)thiazol-4-yl)phenyl)methanesulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1: ethanol / 80 °C

2: palladium on activated charcoal / methanol / 5 h / 20 °C / Inert atmosphere

3: triethylamine / chloroform / 3 h / 20 °C

With palladium on activated charcoal; triethylamine; In methanol; ethanol; chloroform;
DOI:10.1021/jm500833f

Reference yield:

: 14222-60-7
prothionamide

: 1046045-61-7
N-(4-(2-(2-propylpyridin-4-yl)thiazol-4-yl)phenyl)methanesulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1: ethanol / 80 °C

2: palladium on activated charcoal / methanol / 5 h / 20 °C / Inert atmosphere

3: triethylamine / chloroform / 3 h / 20 °C

With palladium on activated charcoal; triethylamine; In methanol; ethanol; chloroform;
DOI:10.1021/jm500833f