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140621-52-9

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140621-52-9 Usage

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 that functions as a stimulant and psychoactive drug. 1-(4-iodophenyl)-N,N-dimethylmethanamine is an iodinated variant of amphetamine and serves as a potent releaser of serotonin, norepinephrine, and dopamine, the key monoamine neurotransmitters in the brain. Due to its effects on neurotransmitter release, 4-iodoamphetamine has been utilized in scientific research to explore the roles of these neurotransmitters in brain function. It also holds potential for application in the treatment of specific psychiatric conditions and in the development of novel pharmaceuticals.

Uses

Used in Scientific Research:
1-(4-iodophenyl)-N,N-dimethylmethanamine is used as a research tool for studying the functions and interactions of monoamine neurotransmitters such as serotonin, norepinephrine, and dopamine in the brain. Its application aids in understanding the complex mechanisms underlying various neurological and psychiatric conditions.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 1-(4-iodophenyl)-N,N-dimethylmethanamine is used as a compound with potential therapeutic applications. Its role as a strong releaser of monoamine neurotransmitters suggests that it may contribute to the development of new medications for the treatment of psychiatric disorders.
Used in Treatment of Psychiatric Disorders:
Although still under investigation, 1-(4-iodophenyl)-N,N-dimethylmethanamine may be used as a therapeutic agent for certain psychiatric conditions. Its ability to modulate the levels of critical neurotransmitters could potentially offer new treatment options for patients suffering from these disorders.

Check Digit Verification of cas no

The CAS Registry Mumber 140621-52-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,6,2 and 1 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 140621-52:
(8*1)+(7*4)+(6*0)+(5*6)+(4*2)+(3*1)+(2*5)+(1*2)=89
89 % 10 = 9
So 140621-52-9 is a valid CAS Registry Number.

140621-52-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-iodophenyl)-N,N-dimethylmethanamine

1.2 Other means of identification

Product number -
Other names N,N-dimethyl-N-(4-iodobenzyl)amine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:140621-52-9 SDS

140621-52-9Relevant articles and documents

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

Aldrich, Courtney C.,Hammerstad, Travis A.,Hegde, Pooja V.,Wang, Kathleen J.

, (2022/02/10)

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

-

Paragraph 321, (2017/01/26)

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

Niu, Song-Lin,Massif, Cedrik,Ulrich, Gilles,Renard, Pierre-Yves,Romieu, Anthony,Ziessel, Raymond

scheme or table, p. 7229 - 7242 (2012/07/03)

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

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