Fomocaine

Base Information

Chemical Name:Fomocaine
CAS No.:17692-39-6
Molecular Formula:C20H25 N O2
Molecular Weight:311.424
Hs Code.:2934999090
European Community (EC) Number:626-114-6
UNII:4XO7A09HQM
DSSTox Substance ID:DTXSID0046222
Nikkaji Number:J10.156G
Wikidata:Q1435626
NCI Thesaurus Code:C65747
ChEMBL ID:CHEMBL1407844
Mol file:17692-39-6.mol

Synonyms:4-(3-(4-(phenoxymethyl)phenyl)propyl)morpholine;fomocain;fomocain hydrochloride;fomocaine;panacain

Suppliers and Price of Fomocaine

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 Fomocaine

Chemical Property:

Vapor Pressure:5.7E-09mmHg at 25°C
Melting Point:52-53°
Refractive Index:1.5614 (estimate)
Boiling Point:469°C at 760 mmHg
PKA:7.44±0.10(Predicted)
Flash Point:153.5°C
PSA：21.70000
Density:1.081g/cm³
LogP:3.46830
XLogP3:3.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:7
Exact Mass:311.188529040
Heavy Atom Count:23
Complexity:303

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1COCCN1CCCC2=CC=C(C=C2)COC3=CC=CC=C3
Therapeutic Function Local anesthetic

Technology Process of Fomocaine

There total 5 articles about Fomocaine 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:

: 69156-39-4
3-<4-(Chloromethyl)phenyl>propyl chloride

: 17692-39-6
fomocaine

Guidance literature:: Multi-step reaction with 2 steps

1: acetone

2: toluene

With acetone; toluene;

Reference yield:

: 139-02-6
sodium phenoxide

: 17692-39-6
fomocaine

Guidance literature:: Multi-step reaction with 2 steps

1: acetone

2: toluene

With acetone; toluene;

Reference yield:

: 55154-44-4
4-[3-(4-Phenoxymethylphenyl)-propyl]-morpholin-N-oxid

: 17692-39-6
fomocaine

Guidance literature:: With D-glucose 6-phosphate; suspension of male Wistar rat liver mitochondria and glucose 6-phosphate dehydrogenase; NADP; magnesium chloride; In various solvent(s); at 37 ℃; for 0.5h; biotransformation;