| Identification | Back Directory | [Name]
S-4-Boc-2-phenylpiperazine | [CAS]
1221274-36-7 | [Synonyms]
S-4-Boc-2-phenylpiperazine
S)-tert-butyl 2-phenylpiperazine-1-carboxylate
(S)-tert-butyl 3-phenylpiperazine-1-carboxylate
tert-butyl (S)-3-phenylpiperazine-1-carboxylate
tert-butyl (3S)-3-phenylpiperazine-1-carboxylate
1-Piperazinecarboxylic acid, 3-phenyl-, 1,1-dimethylethyl ester, (3S)- | [Molecular Formula]
C15H22N2O2 | [MDL Number]
MFCD08685941 | [MOL File]
1221274-36-7.mol | [Molecular Weight]
262.347 |
| Chemical Properties | Back Directory | [density ]
1.071 | [storage temp. ]
Sealed in dry,2-8°C | [InChI]
InChI=1S/C15H22N2O2/c1-15(2,3)19-14(18)17-10-9-16-13(11-17)12-7-5-4-6-8-12/h4-8,13,16H,9-11H2,1-3H3/t13-/m1/s1 | [InChIKey]
HRRFJZULVYGVNJ-CYBMUJFWSA-N | [SMILES]
N1(C(OC(C)(C)C)=O)CCN[C@@H](C2=CC=CC=C2)C1 |
| Questions And Answer | Back Directory | [Application]
Literature reports that (S)-tert-butyloxycarbonyl-2-phenylpiperazine can be used to prepare ROCK inhibitors and bicyclic BET bromo domain inhibitors. |
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