73259-81-1
73259-81-1
Chemical Structure
Boc-L-Dap-OH
- CAS No.: 73259-81-1
- Formula:C8H16N2O4
- Molecular Weight:204.23
IUPAC Name: (S)-3-amino-2-((tert-butoxycarbonyl)amino)propanoic acid
InChIKey: KRJLRVZLNABMAT-YFKPBYRVSA-N
SMILES: O=C(O)[C@H](CN)NC(OC(C)(C)C)=O
Biological Activity: Boc-L-Dap-OH is a Boc-protected derivative of L-2,3-diaminopropionic acid. Boc-L-Dap-OH is an important chiral amino acid derivative. Boc-L-Dap-OH can be generated via the Hofmann rearrangement of Boc-L-asparagine. Boc-L-Dap-OH serves as a starting material for the preparation of BIM analogs[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Boc-L-Dap-OH | 99.21% | Boc-L-Dap-OH is a Boc-protected derivative of L-2,3-diaminopropionic acid. Boc-L-Dap-OH is an important chiral amino acid derivative. Boc-L-Dap-OH can be generated via the Hofmann rearrangement of Boc-L-asparagine. Boc-L-Dap-OH serves as a starting material for the preparation of BIM analogs. | ||||||||||||||||||||
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Structural Analogs
-
Similarity Score 1.00
HY-W014692Boc-D-2,3-diaminopropionic acid -
Similarity Score 0.92
HY-34611Boc-L-2,4-Diaminobutyric acid -
Similarity Score 0.91
HY-W002294(tert-Butoxycarbonyl)-D-serine -
Similarity Score 0.91
HY-W014663(S)-2-((tert-Butoxycarbonyl)amino)-3-hydroxypropanoic acid -
Similarity Score 0.90
HY-79046Boc-L-2-aminobutanoic acid -
Similarity Score 0.88
HY-W008113Boc-L-Homoserine -
Similarity Score 0.88
HY-W017788Boc-D-Homoserine -
Similarity Score 0.88
HY-W008022Boc-Ser(Me)-OH -
Similarity Score 0.87
HY-W014258(R)-2-((tert-Butoxycarbonyl)amino)pent-4-ynoic acid -
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References
- [1]. Küppers J, et al. Tetrahydroimidazo [1, 2‐a] pyrazine Derivatives: Synthesis and Evaluation as Gαq‐Protein Ligands[J]. Chemistry–A European Journal, 2020, 26(55): 12615-12623.
- [2]. Ohyoshi T, et al. Total synthesis of (−)-aplaminal by Buchwald–Hartwig cross-coupling of an aminal[J]. New Journal of Chemistry, 2019, 43(47): 18442-18444.
