2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-1-one

2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-1-one Suppliers list
Company Name: Accela ChemBio Co.,Ltd.  
Tel: 4000665055
Email: marketing@accelachem.com
Company Name: Shanghai Tombiopharma Chemical Co. Ltd.  
Tel: 13391076197
Email: tombiopharma@163.com
Company Name: Wuhan ChemFaces Biochemical Co., Ltd.  
Tel: 18607101326 15172504745
Email: aileen@chemfaces.com
Company Name: EMMX Biotechnology LLC  
Tel: 888-539-0666
Email: info@emmx.com
Company Name: Shanghai YuanYe Biotechnology Co., Ltd.  
Tel: 18916372613
Email: yanzihan@shyuanye.com

2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-1-one manufacturers

2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-1-one Basic information
Product Name:2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-1-one
Synonyms:2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-1-one;1,2,3,4-Tetrahydro-β-carboline-1-one;3,4-Dihydro-β-carboline-1(2H)-one;1,2,3,4-Tetrahydronorharman-1-one;1H-Pyrido[3,4-b]indol-1-one, 2,3,4,9-tetrahydro-;2,3,4,9-tetrahydropyrido[3,4-b]indol-1-one;1,2,3,4-Tetrahydronorharman-1-one, 10 mM in DMSO
CAS:17952-82-8
MF:C11H10N2O
MW:186.21
EINECS:241-878-7
Product Categories:
Mol File:17952-82-8.mol
2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-1-one Structure
2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-1-one Chemical Properties
Melting point 183-185 °C
Boiling point 529.2±39.0 °C(Predicted)
density 1.318±0.06 g/cm3(Predicted)
solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
form Cryst.
pka15.48±0.20(Predicted)
Safety Information
MSDS Information
2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-1-one Usage And Synthesis
Uses1,2,3,4-Tetrahydronorharman-1-one is a manzamine alkaloid with activity against infectious and tropical parasitic diseases from an Indonesian sponge[1].
PreparationTryptamine 380 (9.0 g, 56.2 mmol) and triethylamine (13.8 g, 136.3 mmol) were dissolved in warm toluene (800 mL). Under vigorous stirring, a solution of triphosgene (6.7 g, 22.6 mmol) in toluene (35 mL) was added dropwise and the mixture was stirred for a further 20 min at room temperature. Then, HBr (30% in acetic acid; 13 mL) was added and the mixture was refluxed for 30 min. After cooling to room temperature, water (300 mL) and ethyl acetate (300 mL) were added and, after separation of the layers, the aqueous phase was extracted once more with ethyl acetate (300 mL). The combined organic layers were dried over magnesium sulfate and concentrated in vacuo. The residue was recrystallized from methanol/ethyl acetate (1:1) to afford 7.74 g (74%) of 2,3,4,9-tetrahydro-1H-pyrido[ 3,4-b]indol-1-one 382 as a white solid; mp 184°C.
References[1] Karumanchi V Rao, et al. New manzamine alkaloids with activity against infectious and tropical parasitic diseases from an Indonesian sponge. J Nat Prod. 2003 Jun;66(6):823-8. DOI:10.1021/np020592u
2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-1-one Preparation Products And Raw materials
Preparation Products2-[2-(Methylamino)benzoyl]-3,4-dihydro-β-carboline-1(2H)-one-->2,9-dihydropyrido[3,4-b]indol-1-one
Tag:2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-1-one(17952-82-8) Related Product Information
1-Oxo-2,3,4,9-tetrahydro-1H-B-carboline-6-carboxylic acid ethyl ester 6-Nitro-2,3,4,9-tetrahydro-1H-beta-carbolin-1-one 6-Methyl-2,3,4,9-tetrahydro-1H-beta-carbolin-1-one 6-Iodo-2,3,4,9-tetrahydro-β-carbolin-1-one 1-Oxo-2,3,4,9-tetrahydro-1H-B-carboline-6-carboxylic acid 6-chloro-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-1-one 2,3,4,9-tetrahydro-6-methoxy-1H-pyrido[3,4-b]indol-1-one AKOS BB-9342 AKOS BB-9155 B 193 AKOS BB-9343 2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-1-one 1H-Pyrido(3,4-b)indole-1,3(2H)-dione, 4,9-dihydro-2-(2-(4-(2-pyrimidin yl)-1-piperazinyl)ethyl)-