1421-19-8 ((1H-Pyrrolo[1,2-a]indole,2,3-dihydro-)

快速询单

结构式：

1H-Pyrrolo[1,2-a]indole,2,3-dihydro-MOL文件

CAS号：

1421-19-8

英文名称：

1H-Pyrrolo[1,2-a]indole,2,3-dihydro-

分子式：

C₁₁H₁₁N

分子量：

157.211742639542

1H-Pyrrolo[1,2-a]indole,2,3-dihydro-(1421-19-8)名称与标识符

名称

英文别名：

1H-Pyrrolo[1,2-a]indole,2,3-dihydro-;1,2-Trimethyleneindole;1H-Indole, 1,2-(1,3-propanediyl)-;2,3-Dihydro-1H-pyrrolo[1,2-a]indole;RJXOMHFQIVWQTQ-UHFFFAOYSA-N;SCHEMBL761931;1,2,3,9-tetrahydro-pyrrolo[1,2-a]indole;1H-Pyrrolo[1,2-a]indole, 2,3-dihydro-;1421-19-8;2,3-dihydro-1H-3a-azacyclopenta[a]indene;DTXSID401294915;2,3-dihydro-1H-3a-azacyclopenta[alpha]indene;2,3-dihydro-1H-pyrrolo[1,2-a]indol;

标识符

InChIKey：

RJXOMHFQIVWQTQ-UHFFFAOYSA-N

Inchi：

1S/C11H11N/c1-2-6-11-9(4-1)8-10-5-3-7-12(10)11/h1-2,4,6,8H,3,5,7H2

SMILES：

N12C3C=CC=CC=3C=C1CCC2

1H-Pyrrolo[1,2-a]indole,2,3-dihydro-(1421-19-8)物化性质

计算特性

精确分子量 : 157.089149355g/mol
氢键供体数量 : 0
氢键受体数量 : 0
可旋转化学键数量 : 0
同位素质量 : 157.089149355g/mol
重原子数量 : 12
复杂度 : 178
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） : 2.4
拓扑分子极性表面积 : 4.9Å²

1H-Pyrrolo[1,2-a]indole,2,3-dihydro-(1421-19-8)推荐厂家更多厂家(2)

公司名称	手机号/电话	联系人	QQ	微信	询单
郑州阿尔法化工有限公司	15324716602 0371-55013243	刘经理	2853979810		询单
上海人兮科技有限公司	17717059219 021-67759270	任小姐	1479352695		询单

1H-Pyrrolo[1,2-a]indole,2,3-dihydro-(1421-19-8)相关文献

1. The preparation of 2,3-dihydro-1H-pyrrolo[1,2-a]indole, 2,3-dihydro-9-methyl-1H-pyrrolo[1,2-a]indole, 1,2,2a,3,4,5-hexahydropyrrolo[3,2,1-jk]carbazole, and 2,3,3a,4,5,6-hexahydro-1H-pyrido[3,2,1-jk]carbazole
A. Sydney Bailey,Peter W. Scott,Marazban H. Vandrevala J. Chem. Soc. Perkin Trans. 1 1980 97
2. Expedient synthesis of densely substituted pyrrolo[1,2-a]indoles
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3. Diastereo- and enantioselective construction of biologically important pyrrolo[1,2-a]indole scaffolds via catalytic asymmetric [3 + 2] cyclodimerizations of 3-alkyl-2-vinylindoles
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4. Recent advances in the synthesis of pyrrolo[1,2-a]indoles and their derivatives
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5. Metal-free polychloromethyl radical-initiated cyclization of unactivated N-allylindoles towards pyrrolo[1,2-a]indoles
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6. Scandium-catalyzed tandem selective oxirane ring-opening/Friedel–Crafts alkylation: a facile access to [1,4]oxazino[4,3-a]indoles and 3,4-dihydro-1H-pyrrolo[2,1-c][1,4]oxazines
Lai Wei,Lu Liu,Junliang Zhang Org. Biomol. Chem. 2014 12 6869
7. Synthesis of 1,2-fused indoles by radical cyclisation1
Christopher J. Moody,Claire L. Norton Synthesis of 12-fused indoles by radical cyclisation1. Christopher J. Moody Claire L. Norton J. Chem. Soc. Perkin Trans. 1 1997 2639
8. Recent synthetic journey on pyrrole-fused compounds
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9. Controlling the rates of reductively-activated elimination from the (indol-3-yl)methyl position of indolequinones
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10. Direct synthesis of annulated indoles through palladium-catalyzed double alkylations
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960化工网为您提供1H-Pyrrolo[1,2-a]indole,2,3-dihydro-专业化合物百科信息，包括中文名，英文名，分子式，分子量，以及该化合物的CasNo.1421-19-8,相关理化性质;并提供了优质生产厂家信息包括厂家名称和联系方式等。 WAP版:1421-19-8 国际站:1421-19-8