56153-01-6

Basic information

• Product Name: p-(N,N-dimethylamino)phenethyl bromide
• Synonyms: p-(N,N-dimethylamino)phenethyl bromide
• CAS NO: 56153-01-6
• Molecular Weight: 228.132
• Mol File: 56153-01-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: p-(N,N-dimethylamino)phenethyl bromide(CAS DataBase Reference)
• NIST Chemistry Reference: p-(N,N-dimethylamino)phenethyl bromide(56153-01-6)
• EPA Substance Registry System: p-(N,N-dimethylamino)phenethyl bromide(56153-01-6)

Safety Data

• Hazardous Substances Data: 56153-01-6(Hazardous Substances Data)

Upstream product

• 50438-75-0 2-(4-dimethylaminophenyl)ethyl alcohol 
• 17078-28-3 2-[4-(dimethylamino)phenyl]acetic acid 

Downstream Products

• 2039-80-7 N,N-dimethy-4-vinylaniline 
• 613233-78-6 (+)-octahydro-3,6α-dimethyl-3,12-epoxy-9β-(3'-(p-N,N-dimethylaminophenyl)propyl)-12H-pyrano[4,3j]-1,2-benzodioxepin-10(3H)-one 
• 613233-72-0 (+)-octahydro-3,6α-dimethyl-3,12-epoxy-9β-(3'-(p-N,N-dimethylaminophenyl)propyl)-12H-pyrano[4,3j]-1,2-benzodioxepin-10(3H)-one 
• 613233-77-5 C₂₅H₃₇NO₅ 
• 613233-61-7 (+)-octahydro-3,6α-dimethyl-3,12-epoxy-9α-(3'-(p-N,N-dimethylaminophenyl)propyl)-12H-pyrano[4,3j]-1,2-benzodioxepin-10(3H)-one 
• 63732-69-4 17-(4-dimethylamino-phenethyl)-morphinan-3-ol 

Relevant articles and documents

Structure-activity relationships of the antimalarial agent artemisinin. 8. Design, synthesis, and CoMFA studies toward the development of artemisinin-based drugs against leishmaniasis and malaria

Artemisinin (1) and its analogues have been well studied for their antimalarial activity. Here we present the antimalarial activity of some novel C-9-modified artemisinin analogues synthesized using artemisitene as the key intermediate. Further, antileish

ARTEMISININ-BASED PEROXIDE COMPOUNDS AS BROAD SPECTRUM ANTI-INFECTIVE AGENTS

Described herein is the synthesis, bioassay results and utility of new C-9 and C-10 substituted artemisinin derivatives with easily functionalizable groups attached to the artemisinin skeleton through carbon chain or heteroatoms. Described also is the demonstration of this class of compounds for their broad-spectrum anti-parasitic activity. Certain of these analogs possess noticeable cytotoxicity deliberately focused on treatment of cancerous diseases.