吲哚-4-羧酸

小分子

吲哚-4-甲酸

SCHEMBL40257 | 1h-4-indolecarboxylic acid | AC-3145 | indol-4-yl carboxylic acid | NCGC00324814-01 | FT-0602312 | SY004026 | AB01320195-02 | AKOS000265423 | E0013 | EN300-41008 | 4-INDOLECARBOXYLIC ACID | DTXSID60344230 | 1H-Indole-4-carboxylic acid | PB1

Indole-4-carboxylic Acid

I418719-100g

100g

≥97%

常规运输

吡咯羧酸和吲哚的叔丁酯可以很容易的通过直接处理N,N-二甲基甲酰胺二叔丁基乙缩醛来制备。 Product Application： Reactant for preparation of substituted indole derivatives as histamine H3 antagonists Reactant for preparation of potent and selective inhibitors of human reticulocyte 15-lipoxygenase-1 Reactant for preparation of inhibitors of Gli1-mediated transcription in Hedgehog pathway Reactant for preparation of pyridinyl carboxylates as SARS-CoV 3CL proinhibitors Reactant for preparation of substituted bipiperidinylmethyl amides as CCR3 membrane binding ligands Reactant for preparation of indole amide hydroxamic acids as potent inhibitors of histone deacetylases Reactant for preparation of 2-[[[4′-chloro-[1,1-biphenyl]-4-yl]thio]methyl]-N-hydroxybutanamide derivatives as specific metalloproteinase

2124-55-2

C9H7NO2

161.16 g/mol

22(5)3,43

MFCD00009739

595229

C1=CC(=C2C=CNC2=C1)C(=O)O

1H-indole-4-carboxylic acid

1S/C9H7NO2/c11-9(12)7-2-1-3-8-6(7)4-5-10-8/h1-5,10H,(H,11,12)

ROGHUJUFCRFUSO-UHFFFAOYSA-N

C1=CC(=C2C=CNC2=C1)C(=O)O

504759430

209.0 ~214.0℃

2

2

1

161.048 Da

161.048 Da

53.100 Ų

12

0

193.000

0

1

1.300

129484