推薦產品
品質等級
化驗
97%
mp
197-200 °C (dec.) (lit.)
官能基
carboxylic acid
SMILES 字串
Cn1cc(C(O)=O)c2ccccc12
InChI
1S/C10H9NO2/c1-11-6-8(10(12)13)7-4-2-3-5-9(7)11/h2-6H,1H3,(H,12,13)
InChI 密鑰
HVRCLXXJIQTXHC-UHFFFAOYSA-N
一般說明
1-Methylindole-3-carboxylic acid is an indole derivative that can be prepared by the oxidation of 1-methylindole-3-aldehyde with alkaline potassium permanganate.
應用
- Reactant for preparation of bisindolyl pyrimidinones analogs of PKC inhibitor LY333531
- Reactant for preparation of (heteroaryl)(carboxamido)arylpyrrole derivatives as Cdc7 kinase inhibitors, antitumor and antiproliferative agents
- Reactant for preparation of (pyrrolidinylmethoxy)cyclohexanecarboxylic acids as antigen-4 (VLA-4) antagonists
- Reactant for preparation of EphB3 receptor tyrosine kinase inhibitors
- Reactant for preparation of pyrazolodiazepine derivatives as human P2X7 receptor antagonists
- Reactant for preparation of potent nonpeptidic urotensin II receptor agonists
- Reactant for preparation of pyrrolizidine esters, amides, and ureas as 5-HT4 receptor ligands
訊號詞
Warning
危險聲明
危險分類
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
11 - Combustible Solids
水污染物質分類(WGK)
WGK 3
閃點(°F)
Not applicable
閃點(°C)
Not applicable
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
Reaction of Some Indole Ketones with Iodine and Pyridine.
The Journal of Organic Chemistry, 27(8), 2940-2942 (1962)
Desulfurization of Thiiranes with Iodine.
The Journal of Organic Chemistry, 27(80, 2942-2943 (1962)
Neurogastroenterology and motility : the official journal of the European Gastrointestinal Motility Society, 31(10), e13598-e13598 (2019-04-24)
Activating luminal 5-HT4 receptors results in the release of 5-HT from enterochromaffin cells into the lamina propria to modulate colonic motility. Our aim was to evaluate characteristics of colonic motor patterns involved in the prokinetic effects of intraluminal prucalopride in
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