1225826-38-9

Basic information

• Product Name: 4-tert-butyl-N-nonylaniline
• Synonyms: 4-tert-butyl-N-nonylaniline
• CAS NO: 1225826-38-9
• Molecular Weight: 275.478
• Mol File: 1225826-38-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 4-tert-butyl-N-nonylaniline(CAS DataBase Reference)
• NIST Chemistry Reference: 4-tert-butyl-N-nonylaniline(1225826-38-9)
• EPA Substance Registry System: 4-tert-butyl-N-nonylaniline(1225826-38-9)

Safety Data

• Hazardous Substances Data: 1225826-38-9(Hazardous Substances Data)

Upstream product

• 1746-23-2 4-tert-Butylstyrene 
• 80077-60-7 1-azidononane 
• 19099-48-0 1,1-bis(4-t-butylphenyl)methane 

Relevant articles and documents

Method for synthesizing heteroatom- substituted aromatic compound from styrene compound

The invention discloses a method for synthesizing a heteroatom-substituted aromatic compound from a styrene compound, which comprises the following steps of: mixing a styrene compound with a general formula (I) and a heteroatom-containing compound with a general formula (II), and reacting in the presence of an acid additive and an organic solvent to obtain a heteroatom-substituted compound with ageneral formula (III). According to the synthesis method disclosed by the invention, a large amount of styrene compounds are used as raw materials and react to generate aromatic amine or phenol compounds under the action of no metal catalysis; and compared with the traditional aromatic amine and phenol synthesis method, the method has the advantages of high yield, simple conditions, low waste discharge amount, no metal participation, simple reaction equipment, easiness in industrial production and the like.

FeCl2-promoted cleavage of the unactivated C-C bond of alkylarenes and polystyrene: Direct synthesis of arylamines

Ironing it out: An efficient and convenient nitrogenation strategy involving C-C bond cleavage for the straightforward synthesis of versatile arylamines is presented. Various alkyl azides and alkylarenes, including the common industrial by-product cumene, react using this protocol. Moreover, this method provides a potential strategy for the degradation of polystyrene. Copyright