HCID6998013

tert-butyl N-[(2S)-1-oxo-3-phenylpropan-2-yl]carbamate

C14H19NO3249.3 g/molCAS 72155-45-4

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IDENTITY

结构与身份

标准SMILES: CC(C)(C)OC(=O)N[C@H](C=O)Cc1ccccc1
InChIKey: ZJTYRNPLVNMVPQ-LBPRGKRZSA-N
分子式: C14H19NO3
平均分子量: 249.3 g/mol
单同位素质量: 249.13649347

COMPUTED

结构计算性质

等待补全

XLogP: 2.5
极性表面积: 55.4 Å²
氢键供体: 1
氢键受体: 3
可旋转键: 6
重原子: 18
形式电荷: 0
复杂度: 277

物化、安全与法规信息正在同步。

ALIASES

名称与别名

共 57 条

tert-butyl N-[(2S)-1-oxo-3-phenylpropan-2-yl]carbamatetert-butyl N-((2S)-1-oxo-3-phenylpropan-2-yl)carbamateRefChem:894916675-936-1N-Boc-L-phenylalaninal72155-45-4boc-phe-choboc-l-phenylalaninalN-Boc-phenylalaninalMFCD00143854(S)-tert-Butyl (1-oxo-3-phenylpropan-2-yl)carbamateCHEMBL94327(S)-(-)-2-(tert-Butoxycarbonylamino)-3-phenylpropanaltert-Butyl (S)-(1-oxo-3-phenylpropan-2-yl)carbamateBoc-phenylalaninal(S)-tert-butyl 1-oxo-3-phenylpropan-2-ylcarbamateN-[(1S)-1-Formyl-2-phenylethyl]carbamic Acid 1,1-Dimethylethyl Ester;Boc-L-pheny lalaninalCarbamic acid, [(1S)-1-formyl-2-phenylethyl]-, 1,1-dimethylethyl esterSCHEMBL7094

REACTIONS

参与反应

35 条

uspto-grants-2013_09 · 10.6084/m9.figshare.5104873.v1 · US08524753B2

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uspto-grants-1997_04 · 10.6084/m9.figshare.5104873.v1 · US05616714

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uspto-grants-1997_01 · 10.6084/m9.figshare.5104873.v1 · US05597926

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uspto-grants-1997_07 · 10.6084/m9.figshare.5104873.v1 · US05648497

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uspto-grants-1999_01 · 10.6084/m9.figshare.5104873.v1 · US05859012

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uspto-grants-1999_01 · 10.6084/m9.figshare.5104873.v1 · US05859012

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uspto-grants-1998_11 · 10.6084/m9.figshare.5104873.v1 · US05837873

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uspto-grants-2014_06 · 10.6084/m9.figshare.5104873.v1 · US08741938B2

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