I5605
吲哚啉
ReagentPlus®, 99%
别名:
2,3-二氢吲哚, 吲哚啉
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关于此项目
经验公式（希尔记法）:
C8H9N
化学文摘社编号:
分子量:
119.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
207-816-8
Beilstein/REAXYS Number:
111915
MDL number:
Assay:
99%
Form:
liquid
InChI key
LPAGFVYQRIESJQ-UHFFFAOYSA-N
InChI
1S/C8H9N/c1-2-4-8-7(3-1)5-6-9-8/h1-4,9H,5-6H2
SMILES string
C1Cc2ccccc2N1
product line
ReagentPlus®
assay
99%
form
liquid
Quality Level
refractive index
n20/D 1.592 (lit.)
bp
220-221 °C (lit.)
density
1.063 g/mL at 25 °C (lit.)
Application
用作制备以下产品的反应物：
- NOD1 诱导的核因子-κB 活化抑制剂
- 1-磷酸鞘氨醇 4 (S1P4) 受体拮抗剂
- 细胞毒性细胞周期抑制剂
- 2-氨基吡啶类
- 用于蛋白激酶 C (PKC) 成像的 PET 试剂
- 治疗糖尿病高血糖症的钠依赖性葡萄糖协同转运蛋白 2 (SGLT2) 抑制剂
- 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
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
199.4 °F - closed cup
flash_point_c
93 °C - closed cup
ppe
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
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)
Toshiharu Noji et al.
Organic letters, 15(8), 1946-1949 (2013-04-04)
A benzyne-mediated synthesis of substituted indolines and carbazoles was developed. The reaction includes generation of benzyne using Mg(TMP)2·2LiCl as a base, cyclization, and trapping the resulting organomagnesium intermediate with an electrophile to provide a series of substituted indolines and carbazoles
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
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
Ke Chen et al.
Organic & biomolecular chemistry, 10(32), 6600-6606 (2012-07-17)
A palladacycle-catalyzed tandem Heck-intramolecular aza-Michael reaction protocol has been developed for the one-pot synthesis of 1-substituted isoindolines from N-unprotected 2-bromobenzylamines and acrylates with high yields.
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