alpha-Methylnaphthalene-1-acetonitrile

Base Information

Chemical Name:alpha-Methylnaphthalene-1-acetonitrile
CAS No.:24168-42-1
Molecular Formula:C13H11 N
Molecular Weight:181.237
Hs Code.:2926909090
European Community (EC) Number:246-049-3
DSSTox Substance ID:DTXSID00946994
Nikkaji Number:J287.174B
Mol file:24168-42-1.mol

Synonyms:alpha-Methylnaphthalene-1-acetonitrile;2-(naphthalen-1-yl)propanenitrile;24168-42-1;2-naphthalen-1-ylpropanenitrile;EINECS 246-049-3;2-(1'-naphthyl)propionitrile;SCHEMBL10399086;DTXSID00946994;alpha-Methyl-1-naphthaleneacetonitrile;CS-0237767;EN300-1868396

Suppliers and Price of alpha-Methylnaphthalene-1-acetonitrile

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

AK Scientific
alpha-Methylnaphthalene-1-acetonitrile
10g
$ 4075.00

AK Scientific
alpha-Methylnaphthalene-1-acetonitrile
1g
$ 1024.00

Total 6 raw suppliers

Chemical Property of alpha-Methylnaphthalene-1-acetonitrile

Chemical Property:

Boiling Point:333.1°Cat760mmHg
Flash Point:172.7°C
PSA：23.79000
Density:1.085g/cm³
LogP:3.46688
XLogP3:3.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:181.089149355
Heavy Atom Count:14
Complexity:237

Purity/Quality:

99% ^*data from raw suppliers

alpha-Methylnaphthalene-1-acetonitrile ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C#N)C1=CC=CC2=CC=CC=C21

Technology Process of alpha-Methylnaphthalene-1-acetonitrile

There total 25 articles about alpha-Methylnaphthalene-1-acetonitrile 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: 86.0%

: 132-75-2
naphthalen-1-ylacetonitrile

: 74-88-4
methyl iodide

: 24168-42-1
2-(naphthalen-1-yl)propanenitrile

Guidance literature:: naphthalen-1-ylacetonitrile; With sodium hydride; In N,N-dimethyl-formamide; at 0 ℃; for 0.583333h;

methyl iodide; In N,N-dimethyl-formamide; at 0 - 20 ℃; for 15h;
DOI:10.1039/c2cc36883h

Reference yield: 82.0%

: 321-38-0
1-Fluoronaphthalene

: 107-12-0
propiononitrile

: 24168-42-1
2-(naphthalen-1-yl)propanenitrile

Guidance literature:: With potassium hexamethylsilazane; In tetrahydrofuran; at 20 - 80 ℃; for 1.5h; Concentration; Temperature; Time; Solvent; Inert atmosphere; Schlenk technique; Sealed tube;
DOI:10.1002/asia.201700870

Reference yield: 82.0%

: 941-98-0
1'-naphthacetophenone

: 38622-91-2,36635-61-7
[(p-methylphenyl)sulfonylmethyl]isonitrile

: 24168-42-1
2-(naphthalen-1-yl)propanenitrile

Guidance literature:: With potassium tert-butylate; In 1,2-dimethoxyethane; tert-butyl alcohol; at 0 - 20 ℃;
DOI:10.1016/S0968-0896(99)00236-9