2320-06-1 Usage
Description
1-(1-phenylethyl)-4-(propan-2-yl)benzene, with the molecular formula C21H24 and a molecular weight of 276.42 g/mol, is a substituted benzene derivative featuring a 1-phenylethyl group and a propan-2-yl group attached to the benzene ring. This chemical compound is recognized for its versatile chemical structure, valuable properties, and reactivity, making it a significant contributor to the synthesis of pharmaceuticals and organic materials.
Uses
Used in Pharmaceutical Synthesis:
1-(1-phenylethyl)-4-(propan-2-yl)benzene is used as a key intermediate in the pharmaceutical industry for the synthesis of various drugs. Its unique structure allows for the creation of a wide range of medicinal compounds, contributing to the development of novel treatments for different health conditions.
Used in Organic Material Production:
In the field of organic materials, 1-(1-phenylethyl)-4-(propan-2-yl)benzene serves as a crucial building block. Its incorporation into the production process leads to the creation of advanced materials with specific properties, such as improved stability, reactivity, or functionality, which can be applied in various industrial applications.
Used in Medicinal Chemistry and Drug Discovery Research:
Due to its potential biological activities, 1-(1-phenylethyl)-4-(propan-2-yl)benzene is an important target in medicinal chemistry and drug discovery research. Scientists and researchers utilize its properties to explore new therapeutic avenues and develop innovative drugs with enhanced efficacy and safety profiles.
Check Digit Verification of cas no
The CAS Registry Mumber 2320-06-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,2 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2320-06:
(6*2)+(5*3)+(4*2)+(3*0)+(2*0)+(1*6)=41
41 % 10 = 1
So 2320-06-1 is a valid CAS Registry Number.
2320-06-1Relevant articles and documents
Synthesis of diarylmethanes via a Friedel-Crafts benzylation using arenes and benzyl alcohols in the presence of triphenylphosphine ditriflate
Khodaei, Mohammad Mehdi,Nazari, Ehsan
experimental part, p. 5131 - 5135 (2012/09/22)
Triphenylphosphine ditriflate (TPPD) was found to be an efficient promoter for the Friedel-Crafts benzylation of arenes with benzyl alcohols in CH 2Cl2 at room temperature. The good yields, the 1:1 molar ratio of arene and benzyl alcohol, the benzylation of chlorobenzene as a nonactivated aromatic compound at room temperature, and no by-product formation are the main advantages of this procedure.
Aerobic alcohol oxidation coupled to palladium-catalyzed alkene hydroarylation with boronic esters
Iwai, Yasumasa,Gligorich, Keith M.,Sigman, Matthew S.
, p. 3219 - 3222 (2008/12/23)
(Chemical Equation Presented) An oxidation exercise: An aerobic alcohol oxidation coupled with a regioselective palladium-catalyzed reductive functionalization of styrenes and arylboronic esters has been developed (see scheme). The mechanism is thought to proceed by initial oxidation of the solvent to generate a PdII-hydride species, which subsequently reacts with the alkene and arylboronic ester to ultimately generate a new C-C bond.
