10-Phenyldecanal

Base Information

Chemical Name:10-Phenyldecanal
CAS No.:62232-88-6
Molecular Formula:C16H24O
Molecular Weight:232.366
Hs Code.:
DSSTox Substance ID:DTXSID70577678
Nikkaji Number:J402.572E
Wikidata:Q82467754

Synonyms:10-Phenyldecanal;62232-88-6;Benzenedecanal;SCHEMBL6577356;DTXSID70577678;NNIOZVISSGIISV-UHFFFAOYSA-N

Suppliers and Price of 10-Phenyldecanal

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 0 raw suppliers

Chemical Property of 10-Phenyldecanal

Chemical Property:

PSA：17.07000
LogP:4.54880
XLogP3:5.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:10
Exact Mass:232.182715385
Heavy Atom Count:17
Complexity:170

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)CCCCCCCCCC=O

Technology Process of 10-Phenyldecanal

There total 7 articles about 10-Phenyldecanal 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: 95.0%

: 62607-69-6
10-phenyl-1-decanol

: 62232-88-6
10-phenyl-decanal

Guidance literature:: With oxalyl dichloride; dimethyl sulfoxide; In dichloromethane; at -55 ℃; for 0.25h;
DOI:10.1016/S0968-0896(99)00253-9

Reference yield:

: 53210-25-6
undec-10-en-1-ylbenzene

: 62232-88-6
10-phenyl-decanal

Guidance literature:: With ozone; palladium; In toluene;

Reference yield:

: 43047-93-4
10-tetrahydropyranyloxydecanol

: 62232-88-6
10-phenyl-decanal

Guidance literature:: Multi-step reaction with 5 steps

1: (COCl)2, DMSO, Et₃N / CH₂Cl₂

2: diethyl ether

3: Et₃SiH, CF₃CO₂H

4: NaOH / methanol

5: (COCl)2, DMSO, Et₃N / CH₂Cl₂

With triethylsilane; sodium hydroxide; oxalyl dichloride; dimethyl sulfoxide; triethylamine; trifluoroacetic acid; In methanol; diethyl ether; dichloromethane;
DOI:10.1039/c39860001234