84758-55-4 ((Methyl 2-(tert-butoxycarbonyl)amino-2-methylpropanoate)

CAS号:
84758-55-4
英文名称:
Methyl 2-(tert-butoxycarbonyl)amino-2-methylpropanoate
分子式:
C10H19NO4
分子量:
217.26216340065

Methyl 2-(tert-butoxycarbonyl)amino-2-methylpropanoate(84758-55-4)名称与标识符

名称

英文别名:
Boc-Aib-OMe;N-tert-butoxycarbonyl-α-methylalanine methyl ester;methyl N-(tert-butoxycarbonyl)-2-methyl-alaninate;methyl 2-tert-butoxycarbonylamino-2-methylpropanoate;methyl 2-aminobutoxycarbonyl-2-methylpropanoate;methyl 2-(tert-butoxycarbonylamino)-2-methylpropanoate;N-(tert-butoxycarbonyl)-α-methylalanine methyl ester;;N-[(1,1-Dimethylethoxy)carbonyl]-2-methylalanine methyl ester (ACI);Methyl 2-(tert-butoxycarbonylamino)-2-methylpropanoate;N-tert-Butoxycarbonyl-α-methylalanine methyl ester;SCHEMBL1374814;methyl 2-methyl-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoate;METHYL 2-[(TERT-BUTOXYCARBONYL)AMINO]-2-METHYLPROPANOATE;B-4530;MFCD20484740;AKOS011224071;CS-0154459;OXGSYLWMSHXMLT-UHFFFAOYSA-N;Methyl 2-(Boc-amino)-2-methylpropanoate;Methyl 2-((tert-butoxycarbonyl)amino)-2-methylpropanoate;DB-114651;SY241916;XH1257;methyl 2-{[(tert-butoxy)carbonyl]amino}-2-methylpropanoate;Alanine, N-[(1,1-dimethylethoxy)carbonyl]-2-methyl-, methyl ester;84758-55-4;BS-17634;Methyl2-((tert-butoxycarbonyl)amino)-2-methylpropanoate;Methyl N-(tert-butoxycarbonyl)-2-methylalaninate;

标识符

MDL:
MFCD20484740
InChIKey:
OXGSYLWMSHXMLT-UHFFFAOYSA-N
Inchi:
1S/C10H19NO4/c1-9(2,3)15-8(13)11-10(4,5)7(12)14-6/h1-6H3,(H,11,13)
SMILES:
O=C(NC(C)(C)C(OC)=O)OC(C)(C)C

Methyl 2-(tert-butoxycarbonyl)amino-2-methylpropanoate(84758-55-4)物化性质

实验特性

  • LogP : 1.85360
  • PSA : 64.63000

计算特性

  • 精确分子量 : 217.13100
  • 氢键供体数量 : 1
  • 氢键受体数量 : 5
  • 可旋转化学键数量 : 6
  • 同位素质量 : 217.13140809g/mol
  • 重原子数量 : 15
  • 复杂度 : 253
  • 同位素原子数量 : 0
  • 确定原子立构中心数量 : 0
  • 不确定原子立构中心数量 : 0
  • 确定化学键立构中心数量 : 0
  • 不确定化学键立构中心数量 : 0
  • 共价键单元数量 : 1
  • 疏水参数计算参考值(XlogP) : 1.4
  • 拓扑分子极性表面积 : 64.6Ų

Methyl 2-(tert-butoxycarbonyl)amino-2-methylpropanoate(84758-55-4)推荐厂家 更多厂家(12)

Methyl 2-(tert-butoxycarbonyl)amino-2-methylpropanoate(84758-55-4)合成路线

合成路线:1 步
反应条件:
参考文献:
Synthesis of N-alkyl-Cα,α-dimethylglycine derivatives
Monteiro, Luis S.; Pereira-Lima, Silvia M. M. A.; Pereira, Sofia; Machado, Joao N., ARKIVOC (Gainesville, 2014, (5), 170-180
合成路线:1 步
反应条件:
参考文献:
Benzoazepine-Fused Isoindolines via Intramolecular (3 + 2)-Cycloadditions of Azomethine Ylides with Dinitroarenes
Wales, Steven M. ; Rivinoja, Daniel J.; Gardiner, Michael G. ; Bird, Melissa J.; Meyer, Adam G.; et al, Organic Letters, 2019, 21(12), 4703-4708
合成路线:1 步
反应条件:
参考文献:
Solventless Mechanosynthesis of N-Protected Amino Esters
Konnert, Laure; Lamaty, Frederic; Martinez, Jean; Colacino, Evelina, Journal of Organic Chemistry, 2014, 79(9), 4008-4017
合成路线:1 步
参考文献:
The dominant role of side chains in supramolecular double helical organization in synthetic tripeptides
Sharma, Ankita; Tiwari, Priyanka; Dutt Konar, Anita, Journal of Molecular Structure, 2018, 1161, 44-54
合成路线:1 步
反应条件:
参考文献:
6-Hydrazinopurine 2'-methyl ribonucleosides and their 5'-monophosphate prodrugs as potent hepatitis C virus inhibitors
Gunic, Esmir; Chow, Suetying; Rong, Frank; Ramasamy, Kanda; Raney, Anneke; et al, Bioorganic & Medicinal Chemistry Letters, 2007, 17(9), 2456-2458

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