2-acetyl-8-methyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole

Base Information

• Chemical Name: 2-acetyl-8-methyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole
• CAS No.: 524002-87-7
• Molecular Formula: C14H16N2O
• Molecular Weight: 228.29
• DSSTox Substance ID: DTXSID50351796
• Nikkaji Number: J3.318.842K
• Wikidata: Q82128518
• ChEMBL ID: CHEMBL1542917
• Mol file: 524002-87-7.mol

Synonyms:524002-87-7;2-acetyl-8-methyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole;CHEMBL1542917;1-(8-METHYL-3,4-DIHYDRO-1H-PYRIDO[4,3-B]INDOL-2(5H)-YL)ETHANONE;TimTec1_006237;MLS001206174;SCHEMBL12868355;DTXSID50351796;HMS1551L11;1-(8-Methyl-1,3,4,5-tetrahydro-pyrido[4,3-b]indol-2-yl)-ethanone;BDBM50495385;STK031586;AKOS000664333;AB15544;SMR000524543;EU-0048313;EN300-22423294;Z344133964;1-(8-methyl-1,3,4,5-tetrahydro-2H-pyrido[4,3-b]indol-2-yl)ethanone;1-{8-METHYL-1H,2H,3H,4H,5H-PYRIDO[4,3-B]INDOL-2-YL}ETHAN-1-ONE;1-(8-METHYL-1,3,4,5-TETRAHYDRO-2H-PYRIDO[4,3-B]INDOL-2-YL)-1-ETHANONE

Chemical Property of 2-acetyl-8-methyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole

Chemical Property:

• PSA: 36.10000
• LogP: 2.31880
• XLogP3: 1.8
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 228.126263138
• Heavy Atom Count: 17
• Complexity: 317

Purity/Quality:

98%min ^*data from raw suppliers

2-ACETYL-8-METHYL-2,3,4,5-TETRAHYDRO-1H-PYRIDO[4,3-B]INDOLE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=CC2=C(C=C1)NC3=C2CN(CC3)C(=O)C

Technology Process of 2-acetyl-8-methyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole

There total 1 articles about 2-acetyl-8-methyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 67.0%

N-acetylpiperidin-4-one hydrochloride + p-tolylhydrazine hydrochloride (637-60-5,35467-65-3) → 1-(8-methyl-1,3,4,5-tetrahydro-2H-pyrido[4,3-b]indol-2-yl)ethan-1-one (524002-87-7)

Guidance literature:

In ethanol; for 3h; Reflux;

DOI:10.1021/jm401582c

upstream raw materials:

p-tolylhydrazine hydrochloride