136795-65-8

Basic information

• Product Name: N,N-dimethyl-N-[(E)-2-(4-nitrophenyl)-1-ethenyl]amine
• Synonyms: N,N-dimethyl-N-[(E)-2-(4-nitrophenyl)-1-ethenyl]amine
• CAS NO: 136795-65-8
• Molecular Weight: 192.217
• Mol File: 136795-65-8.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: N,N-dimethyl-N-[(E)-2-(4-nitrophenyl)-1-ethenyl]amine(CAS DataBase Reference)
• NIST Chemistry Reference: N,N-dimethyl-N-[(E)-2-(4-nitrophenyl)-1-ethenyl]amine(136795-65-8)
• EPA Substance Registry System: N,N-dimethyl-N-[(E)-2-(4-nitrophenyl)-1-ethenyl]amine(136795-65-8)

Safety Data

• Hazardous Substances Data: 136795-65-8(Hazardous Substances Data)

Upstream product

• 104-03-0 4-nitrobenzeneacetic acid 
• 4637-24-5 N,N-dimethyl-formamide dimethyl acetal 
• 99-99-0 1-methyl-4-nitrobenzene 

Downstream Products

• 555-21-5 4-Nitrophenylacetonitrile 
• 943987-39-1 2-[2-(4-chlorophenyl)hydrazono]-2-(4-nitrophenyl)acetaldehyde 
• 943987-31-3 1-[4-(4-nitrophenyl)-1-phenyl-1H-3-pyrazolyl]-1-ethanone 
• 64989-98-6 4-(4-Nitrophenyl)-1-phenylpyrazol-3-carbonsaeure-ethylester 
• 943987-34-6 4-(4-nitrophenyl)-1-phenyl-3-phenylcarbamoyl-1H-pyrazole 
• 943987-36-8 [4-(4-nitrophenyl)-1-phenyl-1H-3-pyrazolyl](phenyl)methanone 
• 943987-30-2 1,3-diphenyl-4-(4-nitrophenyl)-1H-pyrazole 

Relevant articles and documents

Intramolecular interactions in nitroamines studied by 1H, 13C, 15N and 17O NMR spectral and quantum chemical methods

1H, 13C, 15N and 17O NMR chemical shifts are used for the characterization of the intramolecular interactions in several nitramines of the Me2N-G-NO2 type. The charge of lone electron pair

Surmounting the resistance against EGFR inhibitors through the development of thieno[2,3-d]pyrimidine-based dual EGFR/HER2 inhibitors

In light of the emergence of resistance against the currently available EGFR inhibitors, our study focuses on tackling this problem through the development of dual EGFR/HER2 inhibitors with improved enzymatic affinities. Guided by the binding mode of the

A MILD METHOD FOR THE CONVERSION OF ACTIVATED ARYL METHYL GROUPS TO CARBOXALDEHYDES VIA THE UNCATALYZED PERIODATE CLEAVAGE OF ANAMINES

A mild procedure for the oxidative cleavage of aryl enamines to aryl aldehydes by periodate without the need for transition metal catalysis is presented.