I5109
吲哚-2-羧酸
98%
别名:
2-吲哚甲酸, 2-羧基吲哚, NSC 16598
质量水平
方案
98%
mp
202-206 °C (lit.)
SMILES字符串
OC(=O)c1cc2ccccc2[nH]1
InChI
1S/C9H7NO2/c11-9(12)8-5-6-3-1-2-4-7(6)10-8/h1-5,10H,(H,11,12)
InChI key
HCUARRIEZVDMPT-UHFFFAOYSA-N
基因信息
human ... SRD5A1(6715)
rat ... Grin2a(24409)
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应用
- (±)-二溴谷胱甘肽和类似物全合成的反应物
- 吡咯里西啶生物碱(±)-颈花脒合成的反应物
- 肾素霉素G类似物立体选择性制备的反应物
- 通过还原吲哚-2-羧酸以及随后的氧化、缩合、还原、酰胺化和Kharasch自由基环化进行螺氧吲哚吡咯烷制备的反应物
- Pd催化的环化反应反应物
- N,N′-（戊烷）二基双[吲哚甲酰胺]和N,N′-[亚苯基双（亚甲基）]双[吲哚甲酰胺]衍生物制备的反应物
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
Stephen P Nighswander-Rempel et al.
Photochemistry and photobiology, 84(3), 613-619 (2008-01-23)
We have synthesized a compound ideally suited to the study of structure-function relationships in eumelanin synthesis. N-methyl-5-hydroxy-6-methoxy-indole (MHMI) has key functional groups strategically placed on the indole framework to hinder binding in the 2, 5, 6 and 7 positions. Thus
R Di Fabio et al.
Journal of medicinal chemistry, 40(6), 841-850 (1997-03-14)
A series of indole-2-carboxylates bearing suitable chains at the C-3 position of the indole nucleus was synthesized and evaluated in terms of in vitro affinity using [3H]glycine binding assay and in vivo potency by inhibition of convulsions induced by N-methyl-D-aspartate
Marine Valette et al.
Physiology and molecular biology of plants : an international journal of functional plant biology, 26(12), 2537-2551 (2021-01-12)
Rhizosphere bacteria, whether phytopathogenic or phytobeneficial, are thought to be perceived by the plant as a threat. Plant Growth-Promoting Rhizobacteria (PGPR), such as many strains of the Azospirillum genus known as the main phytostimulator of cereals, cooperate with host plants
C Kuehm-Caubere et al.
Journal of medicinal chemistry, 40(8), 1201-1210 (1997-04-11)
Series of indole-2-carboxamide and cycloalkeno[1,2-b]indole derivatives were synthesized and evaluated in order to determine the necessary structural requirements for a high inhibition of human LDL copper-induced peroxidation. Various modulations were systematically performed on the indole and cycloalkeno[1,2-b]indole nuclei as well
R Rama Suresh et al.
The Journal of organic chemistry, 77(16), 6959-6969 (2012-07-26)
Two methodologies, one involving Ar-I reactivity and the other through C-H functionalization, for the formation of indolo[2,3-c]pyrane-1-ones via the corresponding allenes, are presented. A highly efficient approach to indolo[2,3-c]pyrane-1-one derivatives through the Pd-catalyzed regioselective annulation of allenes with 3-iodo-1-alkylindole-2-carboxylic acids
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