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- Chemistry
- Asymmetric Synthesis
- Chiral Building Blocks
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- C-H Activation
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- Other Main-group Element
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| Structure chimique | Catalogue N° | CAS N° | Formule | Masse moléculaire |
|---|
 |
BD30085 | 106819-03-8 | C8H17NO2 | 159.23 |
| (R)-2-Aminooctanoic acid | ||||
 |
BD20963 | 479064-94-3 | C14H18FNO4 | 283.30 |
| (R)-3-((tert-Butoxycarbonyl)amino)-3-(4-fluorophenyl)propanoic acid | ||||
 |
BD28239 | 2732-28-7 | C8H9NO | 135.16 |
| 1-(2-Methylpyridin-4-yl)ethanone | ||||
![3-Iodo-1H-pyrrolo[2,3-b]pyridine-5-carbaldehyde](https://file.bldpharm.com/static/upload/proimg/238/900514-07-0.png) |
BD25571 | 900514-07-0 | C8H5IN2O | 272.04 |
| 3-Iodo-1H-pyrrolo[2,3-b]pyridine-5-carbaldehyde | ||||
 |
BD293475 | 209252-17-5 | C24H27NO6 | 425.47 |
| Fmoc-β-HoAsp(OtBu)-OH | ||||
 |
BD300000 | 198476-84-5 | C19H29ClN2O5 | 400.90 |
| Boc-Lysinol(2-Cl-Z) | ||||
 |
BD131069 | 387824-78-4 | C23H24N2O6 | 424.45 |
| Fmoc-D-Dab(Aloc)-OH | ||||
 |
BD300001 | 198543-46-3 | C21H24N2O4S | 400.49 |
| Fmoc-Cysteinol(acm) | ||||
 |
BD145919 | 5147-00-2 | C5H9NO4 | 147.13 |
| O-AC-L-Ser-OH | ||||
 |
BD135442 | 14678-05-8 | C3H4N2O | 84.08 |
| Isoxazol-5-amine | ||||