Niasp

Base Information

Chemical Name:Niasp
CAS No.:124654-22-4
Molecular Formula:C₂₆H₂₉FIN₃O₂
Molecular Weight:561.438
Hs Code.:
Mol file:124654-22-4.mol

Synonyms:(E)-N-(iodoallyl)spiperone;(Z)-N-(iodoallyl)spiperone;N-(iodoallyl)spiperone;N-(iodoallyl)spiperone, (Z) isomer;NIASP

Suppliers and Price of Niasp

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 2 raw suppliers

Chemical Property of Niasp

Chemical Property:

Vapor Pressure:2.62E-18mmHg at 25°C
Boiling Point:679.3°Cat760mmHg
Flash Point:364.6°C
PSA：43.86000
Density:1.51g/cm³
LogP:4.81900
XLogP3:4.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:8
Exact Mass:561.12885
Heavy Atom Count:33
Complexity:696

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CN(CCC12C(=O)N(CN2C3=CC=CC=C3)CC=CI)CCCC(=O)C4=CC=C(C=C4)F
Isomeric SMILES:C1CN(CCC12C(=O)N(CN2C3=CC=CC=C3)C/C=C/I)CCCC(=O)C4=CC=C(C=C4)F

Technology Process of Niasp

There total 1 articles about Niasp 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:

: 124654-18-8,124654-19-9
-3-(tributylstannyl)prop-2-en-1-ol-p-toluenesulfonate

: 749-02-0
spiperone

: 124654-22-4
8-[4-(4-Fluoro-phenyl)-4-oxo-butyl]-3-((E)-3-iodo-allyl)-1-phenyl-1,3,8-triaza-spiro[4.5]decan-4-one

Guidance literature:: With iodine; sodium hydride; Yield given. Multistep reaction; 1.) DMF, room temperature, 5 min, 2.) dichloromethane, room temperature, 1.5 h;
DOI:10.1016/S0040-4039(01)80462-7