1335455-01-0

Basic information

• Product Name: N-(tert-butyl)-2,5-bis(4-chlorophenyl)-1,3-dioxol-4-amine
• Synonyms: N-(tert-butyl)-2,5-bis(4-chlorophenyl)-1,3-dioxol-4-amine
• CAS NO: 1335455-01-0
• Molecular Weight: 364.271
• Mol File: 1335455-01-0.mol

Chemical Properties

• CAS DataBase Reference: N-(tert-butyl)-2,5-bis(4-chlorophenyl)-1,3-dioxol-4-amine(CAS DataBase Reference)
• NIST Chemistry Reference: N-(tert-butyl)-2,5-bis(4-chlorophenyl)-1,3-dioxol-4-amine(1335455-01-0)
• EPA Substance Registry System: N-(tert-butyl)-2,5-bis(4-chlorophenyl)-1,3-dioxol-4-amine(1335455-01-0)

Safety Data

• Hazardous Substances Data: 1335455-01-0(Hazardous Substances Data)

Upstream product

• 119072-55-8 tert-butylisonitrile 
• 104-88-1 4-chlorobenzaldehyde 

Relevant articles and documents

A [bmim]Cl-promoted domino protocol using an isocyanide-based [4+1]-cycloaddition reaction for the synthesis of diversely functionalized 3-Alkylamino-2-Alkyl/aryl/hetero-Aryl indolizine-1-carbonitriles under solvent-free conditions

A domino protocol involving aldehydes, isocyanides and 2-pyridylacetonitrile in the presence of [bmim]Cl as a promoter and solvent for the synthesis of 3-Alkylamino-2-Alkyl/arylindolizine-1-carbonitriles is described. A wide range of alkyl, aryl and heter

SiO2Nanoparticle-catalyzed Facile and Efficient One-pot Synthesis of N-alkyl-2,5-bis[(E)-2-phenylvinyl]-1,3-dioxol-4-amine Under Solvent-free Conditions

1,3-Dioxole-4-amine derivatives have been prepared efficiently in one-pot reaction using nanosized SiO2as a heterogeneous catalyst. The present method does not involve any hazardous organic solvents or catalysts. The high surface-to-volume rati

A simple one-pot synthesis of N-alkyl-2,5-diaryl-1,3-dioxol-4-amines

An efficient procedure for the synthesis of N-alkyl-2,5-diaryl-1,3-dioxol- 4-amines 3 via a one-pot reaction of aromatic aldehydes 2 and alkyl isocyanides 1 at room temperature in good yields is described (Scheme 1, Table). Copyright