13372-41-3

Basic information

• Product Name: Benzene, 1-(1-chloroethyl)-4-(1,1-dimethylethyl)-
• CAS NO: 13372-41-3
• Molecular Formula: C12H17Cl
• Molecular Weight: 196.72
• Mol File: 13372-41-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzene, 1-(1-chloroethyl)-4-(1,1-dimethylethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-(1-chloroethyl)-4-(1,1-dimethylethyl)-(13372-41-3)
• EPA Substance Registry System: Benzene, 1-(1-chloroethyl)-4-(1,1-dimethylethyl)-(13372-41-3)

Safety Data

• Hazardous Substances Data: 13372-41-3(Hazardous Substances Data)

Upstream product

• 101325-12-6 1-(4-tert-butylphenyl)ethanol 
• 107-05-1 3-chloroprop-1-ene 
• 1746-23-2 4-tert-Butylstyrene 

Downstream Products

• 101325-12-6 1-(4-tert-butylphenyl)ethanol 
• 7364-19-4 4-ethyl-tert-butylbenzene 
• 1355201-89-6 4-(1-(4-(tert-butyl)phenyl)ethyl)pyridine 
• 17684-22-9 1,1'-bis(4-tert-butyl-phenyl)-diethyl ether 
• 95022-71-2 2,3-Dimethyl-4-<4'-tert.-butyl-phenyl>-penten-(2) 
• 1203-16-3 <4-tert.-Butyl-α-methylbenzyl>-methyl-ether 
• 15954-44-6 1,1-Dichlor-3-(p-tert.-butyl-phenyl)-buten-⁽¹⁾ 
• 15954-43-5 p-tert.-Butyl-β-methyl-hydrozimtsaeure 

Relevant articles and documents

Nickel-Catalyzed Multicomponent Coupling: Synthesis of α-Chiral Ketones by Reductive Hydrocarbonylation of Alkenes

A nickel-catalyzed, multicomponent regio- and enantioselective coupling via sequential hydroformylation and carbonylation from readily available starting materials has been developed. This modular multicomponent hydrofunctionalization strategy enables the straightforward reductive hydrocarbonylation of a broad range of unactivated alkenes to produce a wide variety of unsymmetrical dialkyl ketones bearing a functionalized α-stereocenter, including enantioenriched chiral α-aryl ketones and α-amino ketones. It uses chiral bisoxazoline as a ligand, silane as a reductant, chloroformate as a safe CO source, and a racemic secondary benzyl chloride or an N-hydroxyphthalimide (NHP) ester of a protected α-amino acid as the alkylation reagent. The benign nature of this process renders this method suitable for late-stage functionalization of complex molecules.

Fungicidal substituted azole derivatives

Compounds having the structural formula STR1 wherein: R can be the same or different and is halogen, hydrogen, C1 -C8 alkyl, C1 -C8 haloalkyl, C3 -C6 cycloalkyl, C7 -C9/sub