CAS 475272-54-9
:(S)-1-Boc-3-isopropylpiperazine
Description:
(S)-1-Boc-3-isopropylpiperazine is a chemical compound characterized by its piperazine core, which is a six-membered ring containing two nitrogen atoms. The "Boc" (tert-butoxycarbonyl) group is a protective group commonly used in organic synthesis to temporarily mask amines, enhancing the compound's stability and reactivity during various chemical reactions. The isopropyl substituent at the 3-position contributes to the compound's steric bulk and can influence its biological activity and solubility. This compound is often utilized in pharmaceutical research and development, particularly in the synthesis of potential drug candidates due to its ability to interact with biological targets. Its chiral nature, indicated by the "(S)" designation, suggests that it may exhibit specific interactions in biological systems, which is crucial for the development of enantiomerically pure drugs. Overall, (S)-1-Boc-3-isopropylpiperazine is significant in medicinal chemistry for its structural features that can be tailored for various applications.
Formula:C12H24N2O2
InChI:InChI=1/C12H24N2O2/c1-9(2)10-8-14(7-6-13-10)11(15)16-12(3,4)5/h9-10,13H,6-8H2,1-5H3/t10-/m0/s1
SMILES:CC(C)[C@@H]1CN(CCN1)C(=O)OC(C)(C)C
Synonyms:- 1-piperazinecarboxylic acid, 3-(1-methylethyl)-, 1,1-dimethylethyl ester, (3R)-
- 2-Methyl-2-propanyl (3R)-3-isopropyl-1-piperazinecarboxylate
- tert-butyl (3R)-3-(propan-2-yl)piperazine-1-carboxylate
- tert-Butyl (3R)-3-isopropylpiperazine-1-carboxylate
- tert-Butyl-(3R)-3-(propan-2-yl)piperazin-1-carboxylat
- tert-Butyl-(3R)-3-isopropylpiperazin-1-carboxylat
- tert-butyl (3R)-3-(1-methylethyl)piperazine-1-carboxylate
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Found 3 products.
(S)-1-N-Boc-3-isopropylpiperazine
CAS:Formula:C12H24N2O2Purity:95%Color and Shape:LiquidMolecular weight:228.3312(S)-1-Boc-3-isopropyl-piperazine
CAS:(S)-1-Boc-3-isopropyl-piperazinePurity:98%Molecular weight:228.336g/mol(S)-1-Boc-3-Isopropylpiperazine
CAS:Formula:C12H24N2O2Purity:98%Color and Shape:SolidMolecular weight:228.336


