N'-(2-chlorophenyl)morpholine-4-carboximidamide

Base Information

Chemical Name:N'-(2-chlorophenyl)morpholine-4-carboximidamide
CAS No.:88897-56-7
Molecular Formula:C₁₁H₁₄ClN₃O
Molecular Weight:239.705
Hs Code.:
DSSTox Substance ID:DTXSID70532565

Synonyms:88897-56-7;N'-(2-chlorophenyl)morpholine-4-carboximidamide;SCHEMBL11170196;DTXSID70532565;AKOS032950736

Suppliers and Price of N'-(2-chlorophenyl)morpholine-4-carboximidamide

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'-(2-chlorophenyl)morpholine-4-carboximidamide

Chemical Property:

XLogP3:1.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:239.0825398
Heavy Atom Count:16
Complexity:254

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:C1COCCN1C(=NC2=CC=CC=C2Cl)N

Technology Process of N'-(2-chlorophenyl)morpholine-4-carboximidamide

There total 1 articles about N'-(2-chlorophenyl)morpholine-4-carboximidamide 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:

: 5344-82-1
o-chlorophenylthiourea

: 88897-56-7
N-(2-Chloro-phenyl)-morpholine-4-carboxamidine

Guidance literature:: Multi-step reaction with 2 steps

1: 96 percent / methanol / 3 h / Ambient temperature

2: 1.) N(C₂H₅)3, 2.) 10percent aq. NaOH / 1.) t-BuOH, reflux, 72 h, 2.) CH₂Cl₂

With sodium hydroxide; triethylamine; In methanol;
DOI:10.1055/s-1988-27606