1,4-Pentanediamine, N1,N1-bis(2-chloroethyl)-N4-(6-chloro-2-methoxy-9-acridinyl)-

Base Information

Chemical Name:1,4-Pentanediamine, N1,N1-bis(2-chloroethyl)-N4-(6-chloro-2-methoxy-9-acridinyl)-
CAS No.:64046-79-3
Molecular Formula:C₂₃H₂₈Cl₃N₃O
Molecular Weight:468.854
Hs Code.:2933990090
UNII:8Y3YQP8GW6
DSSTox Substance ID:DTXSID40982194
Nikkaji Number:J1.122C
Wikidata:Q27104415
Metabolomics Workbench ID:55632
ChEMBL ID:CHEMBL1190232

Synonyms:Acrichine Yperite;Mustard, Quinacrine;Quinacrine Mustard;Yperite, Acrichine

Suppliers and Price of 1,4-Pentanediamine, N1,N1-bis(2-chloroethyl)-N4-(6-chloro-2-methoxy-9-acridinyl)-

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 6 raw suppliers

Chemical Property of 1,4-Pentanediamine, N1,N1-bis(2-chloroethyl)-N4-(6-chloro-2-methoxy-9-acridinyl)-

Chemical Property:

Refractive Index:1.6300 (estimate)
Boiling Point:574.1°Cat760mmHg
Flash Point:301°C
PSA：40.62000
Density:1.271g/cm³
LogP:5.83210
XLogP3:6.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:11
Exact Mass:467.129796
Heavy Atom Count:30
Complexity:494

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:
Safety Statements:A deadly poison by intravenous and intraperitoneal routes. Human mutagenic data reported. When"> − and NOx." target="_blank">A deadly poison by intravenous and intraperitoneal routes. Human mutagenic data reported. When

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(CCCN(CCCl)CCCl)NC1=C2C=C(C=CC2=NC3=C1C=CC(=C3)Cl)OC

Technology Process of 1,4-Pentanediamine, N1,N1-bis(2-chloroethyl)-N4-(6-chloro-2-methoxy-9-acridinyl)-

There total 4 articles about 1,4-Pentanediamine, N1,N1-bis(2-chloroethyl)-N4-(6-chloro-2-methoxy-9-acridinyl)- 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:

: 56100-36-8,56100-37-9,56100-38-0
N¹-(6-chloro-2-methoxy-acridin-9-yl)-N⁴,N⁴-bis-(2-hydroxy-ethyl)-1-methyl-butanediyldiamine

: 64046-79-3
quinacrine

Guidance literature:: With thionyl chloride; chloroform; und anschliessenden Erwaermen;
DOI:10.1021/jo01358a017

Reference yield:

: 86271-50-3
N⁴,N⁴-bis-(2-hydroxy-ethyl)-1-methyl-butanediyldiamine

: 64046-79-3
quinacrine

Guidance literature:: Multi-step reaction with 2 steps

1: phenol

2: chloroform; thionyl chloride / und anschliessenden Erwaermen

With thionyl chloride; chloroform; phenol;
DOI:10.1021/jo01358a017

Reference yield:

: 86-38-4
6,9-dichloro-2-methoxyacridine

: 64046-79-3
quinacrine

Guidance literature:: Multi-step reaction with 2 steps

1: phenol

2: chloroform; thionyl chloride / und anschliessenden Erwaermen

With thionyl chloride; chloroform; phenol;
DOI:10.1021/jo01358a017