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GLPG-0974

Base Information
  • Chemical Name:GLPG-0974
  • CAS No.:1391076-61-1
  • Molecular Formula:C25H25ClN2O4S
  • Molecular Weight:485.004
  • Hs Code.:
GLPG-0974

Synonyms:GLPG-0974

Suppliers and Price of GLPG-0974
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
  • TRC
  • GLPG0974
  • 2.5mg
  • $ 260.00
  • Cayman Chemical
  • GLPG0974
  • 5mg
  • $ 110.00
  • Cayman Chemical
  • GLPG0974
  • 1mg
  • $ 49.00
  • AK Scientific
  • CID57520598
  • 1mg
  • $ 166.00
Total 6 raw suppliers
Chemical Property of GLPG-0974
Chemical Property:
  • Boiling Point:726.3±60.0 °C(Predicted) 
  • Density:1.374±0.06 g/cm3(Predicted) 
Purity/Quality:

99%, *data from raw suppliers

GLPG0974 *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses GLPG 0974 is a potent FFA2 antagonist.
Technology Process of GLPG-0974

There total 12 articles about GLPG-0974 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:
Guidance literature:
4-[[(R)-1-(benzo[b]thiophene-3-carbonyl)-2-methylazetidine-2-carbonyl]-(3-chlorobenzyl)amino]butyric acid methyl ester; With water; sodium hydroxide; In methanol; at 20 ℃; for 15h;
With hydrogenchloride; In methanol; water; pH=2;
Guidance literature:
Multi-step reaction with 8 steps
1.1: potassium hexamethylsilazane / toluene; tetrahydrofuran / 2 h / -78 - 20 °C / Inert atmosphere
1.2: 0.17 h / 20 °C
2.1: hydrogen / palladium on activated charcoal / ethanol / 24 h / 20 °C / Inert atmosphere
3.1: sodium hydroxide; water / ethanol / 15 h / 20 °C
3.2: pH 5
4.1: chiralpak AD-H / hexane; ethanol; formic acid / 20 °C / Resolution of racemate
5.1: 1-chloro-1-(dimethylamino)-2-methyl-1-propene / dichloromethane / 0.5 h / 20 °C / Inert atmosphere
5.2: 2.5 h / -5 - 20 °C
6.1: hydrogenchloride / 1,4-dioxane / 16 h / 20 °C / Inert atmosphere
7.1: triethylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / dichloromethane; tetrahydrofuran / 15 h / 20 °C
7.2: 4.5 h / 20 °C
8.1: sodium hydroxide; water / methanol / 15 h / 20 °C
8.2: pH 2
With hydrogenchloride; 1-chloro-1-(dimethylamino)-2-methyl-1-propene; water; hydrogen; potassium hexamethylsilazane; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; sodium hydroxide; palladium on activated charcoal; In tetrahydrofuran; 1,4-dioxane; methanol; formic acid; ethanol; hexane; dichloromethane; toluene;
Guidance literature:
Multi-step reaction with 7 steps
1.1: hydrogen / palladium on activated charcoal / ethanol / 24 h / 20 °C / Inert atmosphere
2.1: sodium hydroxide; water / ethanol / 15 h / 20 °C
2.2: pH 5
3.1: chiralpak AD-H / hexane; ethanol; formic acid / 20 °C / Resolution of racemate
4.1: 1-chloro-1-(dimethylamino)-2-methyl-1-propene / dichloromethane / 0.5 h / 20 °C / Inert atmosphere
4.2: 2.5 h / -5 - 20 °C
5.1: hydrogenchloride / 1,4-dioxane / 16 h / 20 °C / Inert atmosphere
6.1: triethylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / dichloromethane; tetrahydrofuran / 15 h / 20 °C
6.2: 4.5 h / 20 °C
7.1: sodium hydroxide; water / methanol / 15 h / 20 °C
7.2: pH 2
With hydrogenchloride; 1-chloro-1-(dimethylamino)-2-methyl-1-propene; water; hydrogen; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; sodium hydroxide; palladium on activated charcoal; In tetrahydrofuran; 1,4-dioxane; methanol; formic acid; ethanol; hexane; dichloromethane;
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