Merck
CN
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文件

I5605

Sigma-Aldrich

吲哚啉

ReagentPlus®, 99%

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别名:
2,3-二氢吲哚, 吲哚啉
经验公式（希尔记法）:
C8H9N
CAS号:
496-15-1
分子量:
119.16
Beilstein:
111915
EC 号:
207-816-8
MDL编号:
MFCD00005705
PubChem化学物质编号:
24896074
NACRES:
NA.22

质量水平

200

产品线

ReagentPlus®

检测方案

99%

形式

liquid

折射率

n20/D 1.592 (lit.)

bp

220-221 °C (lit.)

密度

1.063 g/mL at 25 °C (lit.)

SMILES string

C1Cc2ccccc2N1

InChI

1S/C8H9N/c1-2-4-8-7(3-1)5-6-9-8/h1-4,9H,5-6H2

InChI key

LPAGFVYQRIESJQ-UHFFFAOYSA-N

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  • α4β2-烟碱乙酰胆碱受体选择性部分激动剂
  • mGlu4 阳性变构调节剂
  • 细菌生物膜抑制剂
  • 血清素 5-HT6 受体拮抗剂

法律信息

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

储存分类代码

10 - Combustible liquids

WGK

WGK 3

闪点(°F)

199.4 °F - closed cup

闪点(°C)

93 °C - closed cup

个人防护装备

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)

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Matej Baláž et al.
Molecules (Basel, Switzerland), 24(18) (2019-09-22)
Performing solution-phase oximation reactions with hydroxylamine hydrochloride (NH2OH·HCl) carries significant risk, especially in aqueous solutions. In the present study, four N-substituted indole-3-carboxaldehyde oximes were prepared from the corresponding aldehydes by solvent-free reaction with NH2OH·HCl and a base (NaOH or Na2CO3)
Fengtao Zhou et al.
Journal of the American Chemical Society, 134(35), 14326-14329 (2012-08-24)
The first highly enantioselective copper-catalyzed intramolecular Ullmann C-N coupling reaction has been developed. The asymmetric desymmetrization of 1,3-bis(2-iodoaryl)propan-2-amines catalyzed by CuI/(R)-BINOL-derived ligands led to the enantioselective formation of indolines in high yields and excellent enantiomeric excesses. This method was also
Shaolin Zhu et al.
Journal of the American Chemical Society, 134(26), 10815-10818 (2012-06-22)
An enantioselective arylation-cyclization cascade has been accomplished using a combination of diaryliodonium salts and asymmetric copper catalysis. These mild catalytic conditions provide a new strategy for the enantioselective construction of pyrroloindolines, an important alkaloid structural motif that is commonly found
Jan Michael Schuller et al.
Journal of molecular biology, 422(1), 87-99 (2012-06-12)
Fungal indole prenyltransferases (PTs) typically act on specific substrates, and they are able to prenylate their target compounds with remarkably high regio- and stereoselectivity. Similar to several indole PTs characterized to date, the cyclic dipeptide N-prenyltransferase (CdpNPT) is able to
Lei Zhao et al.
Organic letters, 14(8), 2066-2069 (2012-04-03)
An efficient construction of fused indolines with a 2-quaternary center through a palladium-catalyzed intramolecular Heck reaction of N-(2(2-halobenzoxyl)-2,3-disubstituted indoles is disclosed. This protocol provided a straightforward access to diverse fused indolines with good functional group tolerance.
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