Trifenmorph

Base Information

Chemical Name:Trifenmorph
CAS No.:1420-06-0
Molecular Formula:C23H23 N O
Molecular Weight:329.442
Hs Code.:29349990
European Community (EC) Number:215-812-2
UNII:H1IL51K9CW
DSSTox Substance ID:DTXSID6042492
Nikkaji Number:J7.484E
Wikidata:Q27155848
ChEMBL ID:CHEMBL2086832
Mol file:1420-06-0.mol

Synonyms:Frescon;N-tritylmorpholine;trifenmorph;WL 8008

Suppliers and Price of Trifenmorph

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

Sigma-Aldrich
4-TRITYL-MORPHOLINE AldrichCPR
50mg
$ 144.00

Crysdot
4-Tritylmorpholine 97%
10g
$ 1563.00

Crysdot
4-Tritylmorpholine 97%
5g
$ 1116.00

Crysdot
4-Tritylmorpholine 97%
1g
$ 401.00

Total 15 raw suppliers

Chemical Property of Trifenmorph

Chemical Property:

Vapor Pressure:1.14E-07mmHg at 25°C
Melting Point:174-176°, resolidifies and melts again at 185-187°
Refractive Index:1.5614 (estimate)
Boiling Point:432.1°Cat760mmHg
PKA:4.58±0.10(Predicted)
Flash Point:126.5°C
PSA：12.47000
Density:1.12g/cm³
LogP:4.24860
Water Solubility.:20ug/L(20 oC)
XLogP3:4.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:329.177964357
Heavy Atom Count:25
Complexity:339

Purity/Quality:

99.0% ^*data from raw suppliers

4-TRITYL-MORPHOLINE AldrichCPR ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:Xn,N
Statements: 22-50/53
Safety Statements: 60-61

MSDS Files:: SDS file from LookChem

Useful:

Chemical Classes:Pesticides -> Molluscicides
Canonical SMILES:C1COCCN1C(C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4
Uses As molluscicide (against snails carrying bilharzia flukes).

Technology Process of Trifenmorph

There total 8 articles about Trifenmorph 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: 94.0%

: 110-91-8,99108-56-2
morpholine

: 76-83-5
trityl chloride

: 1420-06-0
trifenmorph

Guidance literature:: With triethylamine; In N,N-dimethyl-formamide; at 0 - 20 ℃; for 3h;
DOI:10.1039/c3cc45082a

Reference yield: 44.0%

: 110-91-8,99108-56-2
morpholine

: 78646-25-0
4-dimethylamino-1-N-(triphenylmethyl)pyridinium chloride

: 1420-06-0
trifenmorph

Guidance literature:: With 5-(3-methoxy-3-methylbut-1-yn-1-yl)-1,3-bis(1-(3,5-bis(trifluoromethyl)-phenyl)-1H-1,2,3-triazol-4-yl)benzene; In tetrahydrofuran; at 45 ℃; for 72h;
DOI:10.1002/chem.201203360

Reference yield:

: 76-84-6
triphenylmethyl alcohol

: 1420-06-0
trifenmorph

Guidance literature:: Multi-step reaction with 2 steps

1: acetyl chloride / benzene / Reflux

2: triethylamine / dichloromethane / 18 h / 25 °C

With triethylamine; acetyl chloride; In dichloromethane; benzene;
DOI:10.1016/j.bmcl.2012.08.009