6,7,8,9-tetrahydro-5H-benzo[7]annulen-5-amine

Base Information

• Chemical Name: 6,7,8,9-tetrahydro-5H-benzo[7]annulen-5-amine
• CAS No.: 17910-26-8
• Molecular Formula: C₁₁H₁₅N
• Molecular Weight: 161.247
• Hs Code.: 2921499090
• European Community (EC) Number: 875-166-8
• DSSTox Substance ID: DTXSID20274786
• Nikkaji Number: J2.879.328F
• Mol file: 17910-26-8.mol

Synonyms:6,7,8,9-tetrahydro-5H-benzo[7]annulen-5-amine;17910-26-8;6,7,8,9-tetrahydro-5H-benzocyclohepten-5-ylamine;SCHEMBL2792664;DTXSID20274786;UFBOKWPYNNXYIS-UHFFFAOYSA-N;MFCD09040657;AKOS000128601;SB34382;CS-0341673;EN300-59646;F78367;6,7,8,9-Tetrahydro-5H-benzocycloheptene-5-amine;racemic 6,7,8,9-tetrahydro-5H-benzocyclohepten-5-ylamine

Chemical Property of 6,7,8,9-tetrahydro-5H-benzo[7]annulen-5-amine

Chemical Property:

• PSA: 26.02000
• LogP: 3.11310
• XLogP3: 2.1
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 161.120449483
• Heavy Atom Count: 12
• Complexity: 144

Purity/Quality:

95% ^*data from raw suppliers

6,7,8,9-Tetrahydro-5H-benzocyclohepten-5-ylamine ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1CCC2=CC=CC=C2C(C1)N

Technology Process of 6,7,8,9-tetrahydro-5H-benzo[7]annulen-5-amine

There total 7 articles about 6,7,8,9-tetrahydro-5H-benzo[7]annulen-5-amine 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: 100.0%

1-Benzosuberone (826-73-3) → 6,7,8,9-tetrahydro-5H-benzo[7]annulen-5-amine (17910-26-8)

Guidance literature:

With ammonium acetate; sodium cyanoborohydride; In ethanol; at 130 ℃; for 0.0333333h;

Reference yield:

6,7,8,9-tetrahydrobenzocyclohepten-5-one oxime (90695-87-7) → 6,7,8,9-tetrahydro-5H-benzo[7]annulen-5-amine (17910-26-8)

Guidance literature:

With hydrogen; palladium on activated charcoal; In ethanol; for 72h;

DOI:10.1016/j.bmc.2003.11.007

Reference yield:

benzosuberone oxime (90695-87-7,17910-25-7) → 6,7,8,9-tetrahydro-5H-benzo[7]annulen-5-amine (17910-26-8)

Guidance literature:

With ethanol; sodium; Heating;

upstream raw materials:

benzosuberone oxime

6,7,8,9-tetrahydrobenzocyclohepten-5-one oxime

5-Formamino-6,7,8,9-tetrahydro-5H-benzocyclohepten

1-Benzosuberone

Downstream raw materials:

3,4,5-Trimethoxy-N-(6,7,8,9-tetrahydro-5H-benzocyclohepten-5-yl)-benzamide

2-Phenyl-N-(6,7,8,9-tetrahydro-5H-benzocyclohepten-5-yl)-acetamide

5-(2-Phenyl-1-methyl-aethylamino)-6,7,8,9-tetrahydro-5H-benzocyclohepten

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