2-(4-Methoxyphenyl)butyronitrile

Base Information

Chemical Name:2-(4-Methoxyphenyl)butyronitrile
CAS No.:39066-09-6
Molecular Formula:C₁₁H₁₃NO
Molecular Weight:175.23
Hs Code.:
European Community (EC) Number:662-324-4
Nikkaji Number:J2.049.129I

Synonyms:SCHEMBL11497391;2-(4-methoxyphenyl)butyronitrile;AKOS009458245;DL-2-(4-METHOXYPHENYL)BUTYRONITRILE

Suppliers and Price of 2-(4-Methoxyphenyl)butyronitrile

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Chemical Property of 2-(4-Methoxyphenyl)butyronitrile

Chemical Property:

XLogP3:2.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:175.099714038
Heavy Atom Count:13
Complexity:186

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCC(C#N)C1=CC=C(C=C1)OC

Technology Process of 2-(4-Methoxyphenyl)butyronitrile

There total 12 articles about 2-(4-Methoxyphenyl)butyronitrile 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: 99.0%

: 7677-24-9
trimethylsilyl cyanide

: 5349-60-0
1-(4-methoxyphenyl)-1-propanol

: 39066-09-6
2-(4-methoxy)-phenyl-butyronitrile

Guidance literature:: With indium(III) bromide; In dichloromethane; at 20 ℃; Inert atmosphere;
DOI:10.1021/ol801812a

Reference yield: 97.0%

: 7677-24-9
trimethylsilyl cyanide

: 88932-42-7
4-methoxy-α-ethylbenzyl methyl ether

: 39066-09-6
2-(4-methoxy)-phenyl-butyronitrile

Guidance literature:: With iron(III) chloride; In dichloromethane; at 20 ℃; for 1.5h; Reagent/catalyst; Solvent;
DOI:10.1016/j.tetlet.2013.12.083