4-Phenylnaphthalene-1-carboxaldehyde

Base Information

Chemical Name:4-Phenylnaphthalene-1-carboxaldehyde
CAS No.:133550-74-0
Molecular Formula:C17H12O
Molecular Weight:232.282
Hs Code.:
DSSTox Substance ID:DTXSID20567569
Wikidata:Q82453485
Mol file:133550-74-0.mol

Synonyms:4-Phenylnaphthalene-1-carboxaldehyde;133550-74-0;4-phenylnaphthalene-1-carbaldehyde;4-Phenyl-1-naphthaldehyde;SCHEMBL4864427;DTXSID20567569

Suppliers and Price of 4-Phenylnaphthalene-1-carboxaldehyde

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 4 raw suppliers

Chemical Property of 4-Phenylnaphthalene-1-carboxaldehyde

Chemical Property:

PSA：17.07000
LogP:4.31930
XLogP3:4.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:232.088815002
Heavy Atom Count:18
Complexity:279

Purity/Quality:: 98%min ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C2=CC=C(C3=CC=CC=C32)C=O

Technology Process of 4-Phenylnaphthalene-1-carboxaldehyde

There total 4 articles about 4-Phenylnaphthalene-1-carboxaldehyde 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: 84.0%

: 17422-74-1
3-Formylchromone

: 536-74-3
phenylacetylene

: 133550-74-0
4-phenyl-1-naphthaldehyde

Guidance literature:: With indium(III) triflate; In chlorobenzene; at 80 ℃; for 1h; Reagent/catalyst; Solvent; Temperature; regioselective reaction;
DOI:10.1021/acscatal.1c00629

Reference yield: 83.0%

: 50672-84-9
4-bromo-1-naphthaldehyde

: 98-80-6
phenylboronic acid

: 133550-74-0
4-phenyl-1-naphthaldehyde

Guidance literature:: With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; sodium carbonate; tri tert-butylphosphoniumtetrafluoroborate; In water; toluene; at 100 ℃; for 12h; Inert atmosphere; Schlenk technique;
DOI:10.1002/anie.201708127

Reference yield:

: 4885-02-3
Dichloromethyl methyl ether

: 605-02-7
1-phenylnaphthalene

: 133550-74-0
4-phenyl-1-naphthaldehyde

Guidance literature:: With water; tin(IV) chloride; Yield given. Multistep reaction; 1.) a) CH₂Cl₂, 5 deg C, b) reflux, 16 h, 2.) 10 deg C, 4 h;
DOI:10.1021/jm00111a010