Mtnppp

Base Information

Chemical Name:Mtnppp
CAS No.:97220-08-1
Molecular Formula:C₂₅H₃₂N₂O
Molecular Weight:376.542
Hs Code.:
DSSTox Substance ID:DTXSID80914050
Mol file:97220-08-1.mol

Synonyms:MTNPPP;N-(3-methyl-1-(2-(1,2,3,4-tetrahydro)naphthyl)-4-piperidinyl)-N-phenylpropanamide

Suppliers and Price of Mtnppp

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 3 raw suppliers

Chemical Property of Mtnppp

Chemical Property:

Vapor Pressure:1.16E-10mmHg at 25°C
Boiling Point:513.6°Cat760mmHg
Flash Point:205.2°C
PSA：23.55000
Density:1.104g/cm³
LogP:4.63540
XLogP3:5.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:376.251463648
Heavy Atom Count:28
Complexity:515

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCC(=O)N(C1CCN(CC1C)C2CCC3=CC=CC=C3C2)C4=CC=CC=C4

Technology Process of Mtnppp

There total 12 articles about Mtnppp 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:

: 34737-89-8
1-Benzyl-3-methyl-4-piperidon

: 97220-08-1
trans-N-(3-methyl-1-<2-(1,2,3,4-tetrahydro)naphthyl>-4-piperidinyl)-N-phenylpropanamide

Guidance literature:: Multi-step reaction with 4 steps

1: 5 N HCl, sodium cyanoborohydride, 3 A molecular sieves / methanol / 72 h / Ambient temperature

2: 3 h / Heating

3: 77 percent / conc. HCl, 10percent Pd_.C, H₂ / ethanol / 21 h / 35 °C / 2585.7 Torr

4: 3.6 g / 5N HCl, sodium cyanoborohydride, 3 A molecular sieves / methanol / 84 h / Ambient temperature

With hydrogenchloride; palladium on activated charcoal; 3 A molecular sieve; hydrogen; sodium cyanoborohydride; In methanol; ethanol;

Reference yield:

: 34737-89-8
1-Benzyl-3-methyl-4-piperidon

: 97220-08-1
cis-N-(3-methyl-1-<2-(1,2,3,4-tetrahydro)naphthyl>-4-piperidinyl)-N-phenylpropanamide

Guidance literature:: Multi-step reaction with 4 steps

1: 5 N HCl, sodium cyanoborohydride, 3 A molecular sieves / methanol / 72 h / Ambient temperature

2: 3.5 g / 4 h / Heating

3: 76 percent / conc. HCl, 10percent Pd/C, H₂ / ethanol / 21 h / 35 °C / 2585.7 Torr

4: 5.9 g / 5 N HCl, sodium cyanoborohydride, 3 A molecular sieves / methanol / 84 h / Ambient temperature

With hydrogenchloride; palladium on activated charcoal; 3 A molecular sieve; hydrogen; sodium cyanoborohydride; In methanol; ethanol;

Reference yield:

: 62-53-3
aniline

: 97220-08-1
trans-N-(3-methyl-1-<2-(1,2,3,4-tetrahydro)naphthyl>-4-piperidinyl)-N-phenylpropanamide

Guidance literature:: Multi-step reaction with 4 steps

1: 5 N HCl, sodium cyanoborohydride, 3 A molecular sieves / methanol / 72 h / Ambient temperature

2: 3 h / Heating

3: 77 percent / conc. HCl, 10percent Pd_.C, H₂ / ethanol / 21 h / 35 °C / 2585.7 Torr

4: 3.6 g / 5N HCl, sodium cyanoborohydride, 3 A molecular sieves / methanol / 84 h / Ambient temperature

With hydrogenchloride; palladium on activated charcoal; 3 A molecular sieve; hydrogen; sodium cyanoborohydride; In methanol; ethanol;