CAS 3288-99-1
:Butilfenilacetonitrile
- (p-tert-Butylphenyl)acetonitrile
- 2-(4-tert-Butylphenyl)acetonitrile
- 2-[4-(Tert-Butyl)Phenyl]Ethanenitrile
- 4-(1,1-Dimethylethyl)-Benzeneacetonitril
- 4-(1,1-Dimethylethyl)benzeneacetonitrile
- 4-(Tert-Butyl)Benzyl Cyanide
- 4-Butylphenylacetonitrile
- 4-Tert-Butylphenyl-Acetonitril
- 4-Tert-Butylphenyl-Acetonitrile
- 4-Tert-Butylphenylacetonitrile
- 4-tert-Butylbenzyl cyanide
- Acetonitrile, (p-tert-butylphenyl)-
- Benzeneacetonitrile, 4-(1,1-dimethylethyl)-
- NSC 85354
- P-Tert-Butylbenzylcyanide
- P-Tert-Butylphenylacetonitrile
- p-tert-Butylbenzyl cyanide
- 4-(tert-butyl)phenylacetonitrile
- Butylphenylacetonitrile
- 4-tert-Butylbenzeneacetonitrile
- Vedi altri sinonimi
4-tert-Butylphenylacetonitrile
CAS:Formula:C12H15NPurezza:>98.0%(GC)Colore e forma:Colorless to Almost colorless clear liquidPeso molecolare:173.262-(4-(tert-Butyl)phenyl)acetonitrile
CAS:Formula:C12H15NPurezza:95%Colore e forma:LiquidPeso molecolare:173.25424-(tert-Butyl)phenylacetonitrile
CAS:4-(tert-Butyl)phenylacetonitrileFormula:C12H15NPurezza:98%Colore e forma: light yellow liquidPeso molecolare:173.25g/mol4-tert-Butylbenzylcyanide
CAS:4-tert-Butylbenzylcyanide is a synthetic reagent that is used for the synthesis of ethylene, which is an important chemical in the petrochemical industry. 4-tert-Butylbenzylcyanide can be prepared by a transesterification reaction between alcohols and acetic acid, followed by carbonation. 4-tert-Butylbenzylcyanide has been shown to react with molecular oxygen in solution to form a carbonyl group and fluorescence. This reaction was optimized using molecular orbital theory and localization of electron density.
Formula:C12H15NPurezza:Min. 95%Colore e forma:Clear LiquidPeso molecolare:173.25 g/mol2-[4-(tert-Butyl)phenyl]ethanenitrile
CAS:Formula:C12H15NPurezza:98%Colore e forma:LiquidPeso molecolare:173.2592-(4-tert-Butylphenyl)acetonitrile
CAS:Prodotto controllatoApplications 2-(4-tert-Butylphenyl)acetonitrile has been used in the study of cancer by focusing on inhibiting Akt1 and SCD1
References Imamura, Keisuke, et al.: Bioorganic & Medicinal Chem, 25(14), 3768-3779, (2017). Liu, Yang, et al.: European Journal of Medicinal Chemistry, 138, 543-551, (2017)Formula:C12H15NColore e forma:NeatPeso molecolare:173.25





