N-(cyclopropylmethyl)-1-(naphthalen-1-ylmethyl)-N-propylpiperidine-4-carboxamide

Base Information

Chemical Name:N-(cyclopropylmethyl)-1-(naphthalen-1-ylmethyl)-N-propylpiperidine-4-carboxamide
CAS No.:6578-91-2
Molecular Formula:C₁₅H₉ClN₄O₂S
Molecular Weight:344.781
Hs Code.:
DSSTox Substance ID:DTXSID90387690
Wikidata:Q82182093
ChEMBL ID:CHEMBL5008763

Synonyms:STK090242;N-(cyclopropylmethyl)-1-(naphthalen-1-ylmethyl)-N-propylpiperidine-4-carboxamide;6578-91-2;CHEMBL5008763;DTXSID90387690;AKOS005394539

Suppliers and Price of N-(cyclopropylmethyl)-1-(naphthalen-1-ylmethyl)-N-propylpiperidine-4-carboxamide

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 1 raw suppliers

Chemical Property of N-(cyclopropylmethyl)-1-(naphthalen-1-ylmethyl)-N-propylpiperidine-4-carboxamide

Chemical Property:

Vapor Pressure:4.46E-11mmHg at 25°C
Boiling Point:524.1°C at 760 mmHg
Flash Point:216.3°C
Density:1.113g/cm³
XLogP3:4.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:7
Exact Mass:364.251463648
Heavy Atom Count:27
Complexity:481

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCCN(CC1CC1)C(=O)C2CCN(CC2)CC3=CC=CC4=CC=CC=C43

Technology Process of N-(cyclopropylmethyl)-1-(naphthalen-1-ylmethyl)-N-propylpiperidine-4-carboxamide

There total 2 articles about N-(cyclopropylmethyl)-1-(naphthalen-1-ylmethyl)-N-propylpiperidine-4-carboxamide 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: 62.0%

: 833-47-6
5-(3-nitrophenyl)-1,3,4-thiadiazol-2-amine

: 104-88-1
4-chlorobenzaldehyde

: 6578-91-2
(4-chloro-benzylidene)-[5-(3-nitro-phenyl)-[1,3,4]thiadiazol-2-yl]-amine

Guidance literature:: With sulfuric acid; In ethanol; for 4h; Heating;

Reference yield:

: 121-92-6
3-nitrobenzoic acid

: 6578-91-2
(4-chloro-benzylidene)-[5-(3-nitro-phenyl)-[1,3,4]thiadiazol-2-yl]-amine

Guidance literature:: Multi-step reaction with 2 steps

1: 62 percent / conc. H₂SO₄ / 1 h / Heating

2: 62 percent / conc. H₂SO₄ / ethanol / 4 h / Heating

With sulfuric acid; In ethanol; 1: Cyclization / 2: Condensation;