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- Chemistry
- Asymmetric Synthesis
- Chiral Building Blocks
- Chiral Catalysts, Chiral Ligands and Chiral Reagents
- Chiral Resolution Reagents
- Catalysis Chemistry
- C-H Activation
- Carbon-Donor Ligands
- Cross-Coupling
- Cross-Coupling using Transition Metal Catalysts
- Diketone Ligands
- Hydrogenation
- Main-Group Elements
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- Olefin Metathesis
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- Rare-Earth Elements
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- Chemical Biology
- Conjugation Chemistry
- Glycoscience
- Linkers and Crosslinkers
- Nucleic Acid Chemistry
- PEGylation
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- Photolabile Protecting Group
- Heterocyclic Building Blocks
- Acridinium Series
- Aliphatic Heterocycles
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- Azetidines
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- Chiral nitrogen ligands
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- Nonchiral phosphine ligands
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- Other ligands
- Other Main-group Element
- Photocatalysts
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- Rutheniums
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| Structure chimique | Catalogue N° | CAS N° | Formule | Masse moléculaire |
|---|
 |
BD748951 | 34188-11-9 | C10H23NO5 | 237.29 |
| 14-Amino-3,6,9,12-tetraoxatetradecan-1-ol | ||||
 |
BD302730 | 784105-33-5 | C9H19NO5 | 221.25 |
| 3-(2-(2-(2-Aminoethoxy)ethoxy)ethoxy)propanoic acid | ||||
 |
BD130029 | 370-86-5 | C10H5F3N4O | 254.17 |
| Carbonyl Cyanide 4-(Trifluoromethoxy)phenylhydrazone | ||||
 |
BD760165 | 850090-09-4 | C17H34O8 | 366.45 |
| tert-Butyl 1-hydroxy-3,6,9,12,15-pentaoxaoctadecan-18-oate | ||||
 |
BD760172 | 850090-13-0 | C18H28O7S | 388.48 |
| tert-Butyl 3-(2-(2-(tosyloxy)ethoxy)ethoxy)propanoate | ||||
 |
BD00827192 | 581065-94-3 | C22H36O9S | 476.58 |
| tert-Butyl 1-(tosyloxy)-3,6,9,12-tetraoxapentadecan-15-oate | ||||
 |
BD180631 | 14003-96-4 | C11H8O4 | 204.18 |
| 7-Hydroxy-4-methyl-2-oxo-2H-chromene-8-carbaldehyde | ||||
 |
BD256358 | 39160-70-8 | C12H27NO6 | 281.35 |
| 17-Amino-3,6,9,12,15-pentaoxaheptadecan-1-ol | ||||
![5,7-Dichloro-3-ethylpyrazolo[1,5-a]pyrimidine](https://file.bldpharm.com/static/upload/proimg/419/779353-64-9.png) |
BD26141 | 779353-64-9 | C8H7Cl2N3 | 216.07 |
| 5,7-Dichloro-3-ethylpyrazolo[1,5-a]pyrimidine | ||||
 |
BD760166 | 518044-31-0 | C12H24O6 | 264.32 |
| tert-Butyl 2-(2-(2-(2-hydroxyethoxy)ethoxy)ethoxy)acetate | ||||