Propyl nicotinate

Base Information

Chemical Name:Propyl nicotinate
CAS No.:7681-15-4
Molecular Formula:C9H11NO2
Molecular Weight:165.192
Hs Code.:
European Community (EC) Number:231-662-0
NSC Number:78447
UNII:80CZF4GX8N
DSSTox Substance ID:DTXSID50227629
Nikkaji Number:J191.631I
Wikidata:Q27269141

Synonyms:nicodan;propyl nicotinate

Suppliers and Price of Propyl nicotinate

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 13 raw suppliers

Chemical Property of Propyl nicotinate

Chemical Property:

Vapor Pressure:0.054mmHg at 25°C
Boiling Point:234.1°Cat760mmHg
Flash Point:95.4°C
Density:1.075g/cm³
XLogP3:1.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:165.078978594
Heavy Atom Count:12
Complexity:148

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

Canonical SMILES:CCCOC(=O)C1=CN=CC=C1

Technology Process of Propyl nicotinate

There total 5 articles about Propyl nicotinate 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: 92.0%

: 54-86-4
sodium nicotinate

: 106-94-5
propyl bromide

: 7681-15-4
n-propyl nicotinate

Guidance literature:: In dimethyl sulfoxide; at 30 ℃; for 0.25h; Ionic liquid;
DOI:10.1080/00397910903457357

Reference yield:

: 59-67-6
nicotinic acid

: 7681-15-4
n-propyl nicotinate

Guidance literature:: With pyridine; thionyl chloride; Erhitzen des Reaktionsgemisches auf 100grad und nachfolgenden Erhitzen mit Propan-1-ol;
DOI:10.1021/ja01223a028