140621-52-9

Basic information

• Product Name: 1-(4-iodophenyl)-N,N-dimethylmethanamine
• Synonyms: 1-(4-iodophenyl)-N,N-dimethylmethanamine
• CAS NO: 140621-52-9
• Molecular Weight: 261.105
• Mol File: 140621-52-9.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 1-(4-iodophenyl)-N,N-dimethylmethanamine(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-iodophenyl)-N,N-dimethylmethanamine(140621-52-9)
• EPA Substance Registry System: 1-(4-iodophenyl)-N,N-dimethylmethanamine(140621-52-9)

Safety Data

• Hazardous Substances Data: 140621-52-9(Hazardous Substances Data)

Usage

General Description

1-(4-iodophenyl)-N,N-dimethylmethanamine, also known as 4-iodoamphetamine, is a chemical compound with the molecular formula C11H15IN. It is a substituted amphetamine derivative and acts as a stimulant and psychoactive drug. 4-iodoamphetamine is an iodinated derivative of amphetamine and is a strong serotonin/norepinephrine/dopamine releasing agent. It has been used in scientific research as a tool for studying the functions of the various monoamine neurotransmitters such as serotonin, norepinephrine, and dopamine in the brain. The compound may also have potential applications in the treatment of certain psychiatric disorders and the development of new medications. However, it is important to note that 4-iodoamphetamine is a controlled substance in many jurisdictions and its use and distribution are restricted.

Upstream product

• 100-97-0 hexamethylenetetramine 
• 16004-15-2 1-bromomethyl-4-iodobenzene 
• 619-58-9 4-iodobenzoic acid 
• 51934-41-9 4-iodobenzoic acid ethyl ester 
• 124-40-3 dimethyl amine 
• 109-89-7 diethylamine 
• 624-31-7 4-tolyl iodide 
• 506-59-2 N,N-dimethylammonium chloride 

Downstream Products

• 1467-79-4 NCNMe₂ 
• 16004-15-2 1-bromomethyl-4-iodobenzene 
• 36874-95-0 4-(dimethylaminomethyl)benzaldehyde 
• 1391916-73-6 C₃₉H₄₀BF₂IN₄ 
• 1247001-32-6 N,N-dimethyl-1-(4-acetylenylphenyl)methylamine 

Relevant articles and documents

Chemoselective Reduction of Tertiary Amides by 1,3-Diphenyl disiloxane (DPDS)

A convenient procedure for the chemoselective reduction of tertiary amides at room temperature in the presence of air and moisture using 1,3-diphenyldisiloxane (DPDS) is developed. The reaction conditions tolerate a significant number of functional groups including esters, nitriles, secondary amides, carbamates, sulfoxides, sulfones, sulfonyl fluorides, halogens, aryl-nitro groups, and arylamines. The conditions reported are the mildest to date and utilize EtOAc, a preferred solvent given its excellent safety profile and lower environmental impact. The ease of setup and broad chemoselectivity make this method attractive for organic synthesis, and the results further demonstrate the utility of DPDS as a selective reducing agent.

HETERO-HALO INHIBITORS OF HISTONE DEACETYLASE

This invention provides compounds that are inhibitors of HDAC2. The compounds (e.g., compounds according to Formula I, II or any of Compounds 100-128 or any of those in Tables 2 or 3) accordingly are useful for treating, alleviating, or preventing a condition in a subject such as a neurological disorder, memory or cognitive function disorder or impairment, extinction learning disorder, fungal disease or infection, inflammatory disease, hematological disease, or neoplastic disease, or for improving memory or treating, alleviating, or preventing memory loss or impairment.

Water-soluble red-emitting distyryl-borondipyrromethene (BODIPY) dyes for biolabeling

A series of water-soluble red-emitting distyryl-borondipyrromethene (BODIPY) dyes were designed and synthesized by using three complementary approaches aimed at introducing water-solubilizing groups on opposite faces of the fluorescent core to reduce or c