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103273-65-0

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103273-65-0 Usage

Description

1-(3-Chlorophenyl)-2-Methylpropan-2-aMine, also known as 3-Cl-2-Me-2-Phenylaminopropane, is a chemical compound with the molecular formula C10H14ClN. It is a substituted amphetamine that possesses stimulant properties. 1-(3-Chlorophenyl)-2-Methylpropan-2-aMine is typically utilized in the research and development of new medications and drugs, particularly within the fields of neuroscience and pharmacology. It is known to influence the central nervous system, potentially altering mood, cognition, and behavior. Due to its potential for abuse and dependence, this chemical is often regulated and controlled. Ongoing research aims to further elucidate its pharmacological effects and explore its potential therapeutic applications.

Uses

Used in Pharmaceutical Research and Development:
1-(3-Chlorophenyl)-2-Methylpropan-2-aMine is used as a research compound for the development of new medications and drugs, particularly in the field of neuroscience and pharmacology. It aids in understanding the effects of stimulants on the central nervous system and their potential applications in treating various conditions.
Used in Neuroscience Research:
In the field of neuroscience, 1-(3-Chlorophenyl)-2-Methylpropan-2-aMine is used as a research tool to study the mechanisms of action of stimulants on the brain. This helps in gaining insights into mood, cognition, and behavior alterations caused by such compounds.
Used in Regulatory and Control Measures:
Due to its potential for abuse and dependence, 1-(3-Chlorophenyl)-2-Methylpropan-2-aMine is often subject to regulatory and control measures. It is used in the development of policies and guidelines for the safe and responsible use of such substances in medical and research settings.
Used in Ongoing Pharmacological Research:
1-(3-Chlorophenyl)-2-Methylpropan-2-aMine is employed in ongoing pharmacological research to further understand its effects and explore its potential therapeutic uses. This includes investigating its interactions with various biological systems and identifying possible applications in treating specific conditions or disorders.

Check Digit Verification of cas no

The CAS Registry Mumber 103273-65-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,2,7 and 3 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 103273-65:
(8*1)+(7*0)+(6*3)+(5*2)+(4*7)+(3*3)+(2*6)+(1*5)=90
90 % 10 = 0
So 103273-65-0 is a valid CAS Registry Number.

103273-65-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3-chlorophenyl)-2-methylpropan-2-amine

1.2 Other means of identification

Product number -
Other names 3-CHLORO-A,A-DIMETHYL-BENZENEETHANAMINE

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:103273-65-0 SDS

103273-65-0Downstream Products

103273-65-0Relevant articles and documents

Direct Access to Primary Amines from Alkenes by Selective Metal-Free Hydroamination

Du, Yi-Dan,Chen, Bi-Hong,Shu, Wei

supporting information, p. 9875 - 9880 (2021/03/29)

Direct and selective synthesis of primary amines from easily available precursors is attractive yet challenging. Herein, we report the rapid synthesis of primary amines from alkenes via metal-free regioselective hydroamination at room temperature. Ammonium carbonate was used as ammonia surrogate for the first time, allowing for efficient conversion of terminal and internal alkenes into linear, α-branched, and α-tertiary primary amines under mild conditions. This method provides a straightforward and powerful approach to a wide spectrum of advanced, highly functionalized primary amines which are of particular interest in pharmaceutical chemistry and other areas.

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