Nomelidine

Base Information

Chemical Name:Nomelidine
CAS No.:60324-59-6
Molecular Formula:C15H15 Br N2
Molecular Weight:303.201
Hs Code.:2933399090
UNII:FVL27C1DMG
DSSTox Substance ID:DTXSID501024244
Nikkaji Number:J18.359H,J3.024.184C
Wikidata:Q27278232
NCI Thesaurus Code:C75173
ChEMBL ID:CHEMBL287064
Mol file:60324-59-6.mol

Synonyms:3-(4-bromophenyl)-N-methyl-(3-pyiidyl)allylamine oxalate;cholesterol-3-glucose;CPP 199;norzimeldine;norzimelidine;norzimelidine dihydrochloride;norzimelidine dihydrochloride, (Z)-isomer;norzimelidine fumarate (1:1);norzimelidine maleate (1:1);norzimelidine monohydrochloride;norzimelidine, (E)-isomer;norzimelidine, (Z)-isomer

Suppliers and Price of Nomelidine

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

American Custom Chemicals Corporation
NOMELIDINE 95.00%
5MG
$ 496.58

Total 2 raw suppliers

Chemical Property of Nomelidine

Chemical Property:

Vapor Pressure:1.23E-07mmHg at 25°C
Boiling Point:431.1°C at 760 mmHg
Flash Point:214.5°C
PSA：24.92000
Density:1.309g/cm³
LogP:3.88610
XLogP3:3.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:302.04186
Heavy Atom Count:18
Complexity:270

Purity/Quality:

99% ^*data from raw suppliers

NOMELIDINE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CNCC=C(C1=CC=C(C=C1)Br)C2=CN=CC=C2
Isomeric SMILES:CNC/C=C(/C1=CC=C(C=C1)Br)\C2=CN=CC=C2

Technology Process of Nomelidine

There total 7 articles about Nomelidine 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: 56.0%

: 593-51-1
methylamine hydrochloride

: 77470-68-9
(Z)-3-(4-bromophenyl)-3-(3-pyridyl)-2-propenal

: 60324-59-6
Nomelidine

: 91671-08-8
Bis-[(Z)-3-(4-bromo-phenyl)-3-pyridin-3-yl-allyl]-methyl-amine

Guidance literature:: With sodium cyanoborohydride; In methanol; at -15 ℃; for 4h;
DOI:10.1021/jo00196a021

Reference yield:

: 70263-44-4
(Z)-3-(4-bromophenyl)-3-(3-pyridyl) allyl chloride

: 60324-59-6
Nomelidine

Guidance literature:: With methylamine; In ethanol;

Reference yield:

: 56775-88-3
Zimelidine

: 60324-59-6
Nomelidine

Guidance literature:: Multi-step reaction with 2 steps

1: 70 percent / ClCOOCH₂CCl₃ / benzene / 2 h / Heating

2: 12 g / ethanol / 24 h / Ambient temperature

With 2,2,2-Trichloroethyl chloroformate; In ethanol; benzene;
DOI:10.3891/acta.chem.scand.36b-0091