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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
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- Hydrogenation
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- Olefin Metathesis
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- Chemical Biology
- Conjugation Chemistry
- Glycoscience
- Linkers and Crosslinkers
- Nucleic Acid Chemistry
- PEGylation
- Peptide Chemistry
- Photolabile Protecting Group
- Heterocyclic Building Blocks
- Acridinium Series
- Aliphatic Heterocycles
- Aromatic Heterocycles
- Azetidines
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- Other Main-group Element
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| Structure chimique | Catalogue N° | CAS N° | Formule | Masse moléculaire |
|---|
 |
BD144394 | 2491-15-8 | C3H5NO3 | 103.08 |
| N-Formylglycine | ||||
 |
BD21504 | 56558-30-6 | C6H14ClNO2 | 167.63 |
| H-Nva-Ome.HCl | ||||
 |
BD1373 | 86060-81-3 | C21H22N2O5S | 414.47 |
| Fmoc-Cys(Acm)-OH | ||||
 |
BD21483 | 5619-05-6 | C6H14ClNO2 | 167.63 |
| H-DL-Val-OMe.HCl | ||||
 |
BD20924 | 4668-42-2 | C13H15NO6 | 281.26 |
| (S)-3-(((Benzyloxy)carbonyl)amino)-4-methoxy-4-oxobutanoic acid | ||||
 |
BD42061 | 85642-13-3 | C8H16N2O3 | 188.22 |
| Boc-Ala-NH2 | ||||
 |
BD17399 | 10466-61-2 | C6H15ClN2O | 166.65 |
| H-Leu-NH2.HCl | ||||
 |
BD18204 | 13798-75-9 | C20H24N2O8 | 420.41 |
| Boc-Asp(Obzl)-Osu | ||||
 |
BD21975 | 64017-81-8 | C3H9ClN2O | 124.57 |
| H-β-Ala-NH2.HCl | ||||
 |
BD9250 | 84624-27-1 | C26H32N2O6 | 468.54 |
| Boc-Lys(Fmoc)-OH | ||||