Emorfazone

Base Information

Chemical Name:Emorfazone
CAS No.:38957-41-4
Molecular Formula:C11H17N3O3
Molecular Weight:239.274
Hs Code.:2934999090
European Community (EC) Number:254-220-9
UNII:V93U9DH62C
DSSTox Substance ID:DTXSID0022981
Nikkaji Number:J3.186K
Wikidata:Q27291687
NCI Thesaurus Code:C73085
Metabolomics Workbench ID:155697
ChEMBL ID:CHEMBL2103954
Mol file:38957-41-4.mol

Synonyms:4-ethoxy-2-methyl-5-morpholino-3(2H)-pyridazinone;emorfazone;M 73101;M-73101;M73101

Suppliers and Price of Emorfazone

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
EMORFAZONE 95.00%
5MG
$ 497.90

Total 14 raw suppliers

Chemical Property of Emorfazone

Chemical Property:

Vapor Pressure:1.46E-05mmHg at 25°C
Melting Point:89-91°
Refractive Index:1.5700 (estimate)
Boiling Point:366.5°C at 760 mmHg
Flash Point:175.4°C
PSA：56.59000
Density:1.27g/cm³
LogP:0.08060
XLogP3:0
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:3
Exact Mass:239.12699141
Heavy Atom Count:17
Complexity:359

Purity/Quality:

99% ^*data from raw suppliers

EMORFAZONE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC1=C(C=NN(C1=O)C)N2CCOCC2
Description Emorfazone is an analgesic agent with a potency similar to aminopyrine, useful in the treatment of low back pain and similar musculoskeletal disorders.
Uses Emorfazone has been known to comprise of 5α-?reductase inhibitor. It consists of postsurgical adhesion inhibitors that contain anti-inflammatory agents and anticoagulants and hyaluronate.

Technology Process of Emorfazone

There total 1 articles about Emorfazone 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:

: 38957-41-4
emorfazone

Guidance literature:: entspr. 4-Chlor-pyridazinon, Ethanol (Na);

Reference yield: 14.0%

: 38957-41-4
emorfazone

: 116614-72-3
4-ethoxycarbonyl-2-methyl-4-morpholino-3(2H)-pyrazolone

: 116614-71-2
5-(2,3-dihydro-1,4-oxazin-4-yl)-4-ethoxy-2-methyl-3(2H)-pyridazinone

: 116614-73-4
diethyl 1,1'-dimethyl-5,5'-dioxo-1,1',5,5'-tetrahydro-4H,4'H-[4,4'-bipyrazole]-4,4'-dicarboxylate

: 67911-04-0
4-ethoxy-5-(2-hydroxyethylamino)-2-methyl-3(2H)-pyridazinone

Guidance literature:: With 1,3,6,8-tetra-n-butylpyrimido<5,4-g>pteridine-2,4,5,7(1H,3H,6H,8H)-tetrone 10-oxide; In acetonitrile; for 0.5h; Ambient temperature; Irradiation;
DOI:10.1248/cpb.36.1714