(S)-2-(((9H-FLUOREN-9-YL)METHOXY)CARBONYLAMINO)-3-AZIDOPROPANOIC ACID
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- ₹19885.53
- Product name: (S)-2-(((9H-FLUOREN-9-YL)METHOXY)CARBONYLAMINO)-3-AZIDOPROPANOIC ACID
- CAS: 684270-46-0
- MF: C18H16N4O4
- MW: 352.35
- EINECS:
- MDL Number:MFCD11052919
- Synonyms:FMOC-L-BETA-AZIDOALANINE;3-Azido-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-alanine;Fmoc-L-Dap(N3)-OH;3-Azido-N-Fmoc-L-alanine;Fmoc-L-Aza-OH;2-(S)-Fmoc-amino-3-azidopropanoic acid;Nα-Fmoc-Nβ-Azido-L-2,3-diaminopropionic acidSolvate with DIPE≥ 99% (HPLC);(S)-2-(((9H-FLUOREN-9-YL)METHOXY)CARBONYLAMINO)-3-AZIDOPROPANOIC ACID
1 prices
Selected condition:
Brand
- Sigma-Aldrich(India)
Package
- 250MG
- ManufacturerSigma-Aldrich(India)
- Product number714151
- Product descriptionFmoc-β-azido-Ala-OH ≥98.0% (HPLC)
- Packaging250MG
- Price₹19885.53
- Updated2022-06-14
- Buy
| Manufacturer | Product number | Product description | Packaging | Price | Updated | Buy |
|---|---|---|---|---|---|---|
| Sigma-Aldrich(India) | 714151 | Fmoc-β-azido-Ala-OH ≥98.0% (HPLC) | 250MG | ₹19885.53 | 2022-06-14 | Buy |
Properties
Melting point :>155 (dec.)
storage temp. :2-8°C
solubility :DMF (Slightly), DMSO (Slightly), Methanol (Slightly)
form :Solid
color :White to Off-White
optical activity :[α]/D -10.0±1.0°, c = 1 in DMF
InChI :InChI=1/C18H16N4O4/c19-22-20-9-16(17(23)24)21-18(25)26-10-15-13-7-3-1-5-11(13)12-6-2-4-8-14(12)15/h1-8,15-16H,9-10H2,(H,21,25)(H,23,24)/t16-/s3
InChIKey :ZITYCUDVCWLHPG-QEIABERDNA-N
SMILES :C(C1C2=CC=CC=C2C2=CC=CC=C12)OC(=O)N[C@H](C(=O)O)CN=[N+]=[N-] |&1:18,r|
storage temp. :2-8°C
solubility :DMF (Slightly), DMSO (Slightly), Methanol (Slightly)
form :Solid
color :White to Off-White
optical activity :[α]/D -10.0±1.0°, c = 1 in DMF
InChI :InChI=1/C18H16N4O4/c19-22-20-9-16(17(23)24)21-18(25)26-10-15-13-7-3-1-5-11(13)12-6-2-4-8-14(12)15/h1-8,15-16H,9-10H2,(H,21,25)(H,23,24)/t16-/s3
InChIKey :ZITYCUDVCWLHPG-QEIABERDNA-N
SMILES :C(C1C2=CC=CC=C2C2=CC=CC=C12)OC(=O)N[C@H](C(=O)O)CN=[N+]=[N-] |&1:18,r|
Safety Information
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Description
Fmoc-β-azido-Ala-OH chloride is a general N-terminal protected reagent used in the solid phase peptide synthesis. Azido group allows it to undergo copper-mediated click chemistry reactions.It can be used in:
- Synthesis of α-N-acetylgalactosamine (α-GalNAc) linked antifreeze glycopeptides (AFGPs).
- Synthesis of stimuli-responsive multifunctional peptide gatekeepers for drug delivery applications.
- Synthesis of triazole-linked glycopeptides via Cu(I)-catalyzed 1,3-dipolar cycloaddition (CuAAC).
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