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品質等級
化驗
≥95.0% (HPLC)
雜質
≤5.0% water
SMILES 字串
OC(=O)[C@@H]1CCCC(=O)N1
InChI
1S/C6H9NO3/c8-5-3-1-2-4(7-5)6(9)10/h4H,1-3H2,(H,7,8)(H,9,10)/t4-/m0/s1
InChI 密鑰
FZXCPFJMYOQZCA-BYPYZUCNSA-N
應用
(S)-6-Oxo-2-piperidinecarboxylic acid can be used as a reactant to synthesize:
- Functionalized β-lactam N-heterocycles via carboxymethylproline synthase catalyzed cyclization reactions. Pro-(S)-C5 branched [4.3.1] aza-amide bicycles as potential inhibitors for FK506-binding proteins.
- Ethyl (S)-2-(6-oxopiperidin-2-yl)acetate, which is reduced using LiBH4 to produce optically pure hydroxymethyl lactams.
訊號詞
Warning
危險聲明
危險分類
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
11 - Combustible Solids
水污染物質分類(WGK)
WGK 2
閃點(°F)
Not applicable
閃點(°C)
Not applicable
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
Carboxymethylproline synthase catalysed syntheses of functionalised N-heterocycles
Chemical Communications (Cambridge, England), 46(9), 1413-1415 (2010)
Preparation of optically pure ω-hydroxymethyl lactams
Synthetic Communications, 19(20), 3485-3496 (1989)
Rational Design and Asymmetric Synthesis of Potent and Neurotrophic Ligands for FK506-Binding Proteins (FKBPs)
Angewandte Chemie (International ed. in English), 54(1), 345-348 (2015)
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