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CAS

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688362-60-9

1-(4-bromophenyl)prop-2-en-1-amine, also known as 4-bromoamphetamine, is a chemical compound belonging to the phenethylamine class, with the molecular formula C9H10BrN. It is a derivative of amphetamine and is recognized for its psychoactive effects, acting as a monoamine releaser and releasing dopamine, serotonin, and norepinephrine in the brain.

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  • 688362-60-9 Structure

  • Basic information

    1. Product Name: 1-(4-bromophenyl)prop-2-en-1-amine
    2. Synonyms: 1-(4-bromophenyl)prop-2-en-1-amine
    3. CAS NO:688362-60-9
    4. Molecular Formula: C9H10BrN
    5. Molecular Weight: 212.0864
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 688362-60-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-(4-bromophenyl)prop-2-en-1-amine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(4-bromophenyl)prop-2-en-1-amine(688362-60-9)
    11. EPA Substance Registry System: 1-(4-bromophenyl)prop-2-en-1-amine(688362-60-9)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 688362-60-9(Hazardous Substances Data)

688362-60-9 Usage

Uses

Used in Research Chemicals:
1-(4-bromophenyl)prop-2-en-1-amine is used as a research chemical for studying its psychoactive effects and potential applications in various medical conditions. Its ability to release monoamines like dopamine, serotonin, and norepinephrine makes it a subject of interest in neuroscience and pharmacology.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 1-(4-bromophenyl)prop-2-en-1-amine is used as a starting material or intermediate in the synthesis of various drugs targeting the central nervous system. Its stimulant and entactogenic effects are being explored for potential therapeutic uses, although its potential for abuse and adverse effects must be carefully considered.
Used in Medical Treatments:
1-(4-bromophenyl)prop-2-en-1-amine has been studied for its potential as a treatment for various medical conditions related to the central nervous system, such as depression, attention deficit hyperactivity disorder (ADHD), and other mood disorders. Its effects on monoamine neurotransmitters make it a candidate for further research in these areas.

Check Digit Verification of cas no

The CAS Registry Mumber 688362-60-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,8,3,6 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 688362-60:
(8*6)+(7*8)+(6*8)+(5*3)+(4*6)+(3*2)+(2*6)+(1*0)=209
209 % 10 = 9
So 688362-60-9 is a valid CAS Registry Number.

688362-60-9Relevant articles and documents

Flexible synthesis of polyfunctionalised 3-fluoropyrroles

Cogswell, Thomas J.,Donald, Craig S.,Marquez, Rodolfo

supporting information, p. 183 - 190 (2015/12/30)

An efficient and selective approach for the synthesis of polyfunctionalised 3-fluoropyrroles has been developed starting from commercial aldehydes. The methodology is concise, efficient and allows for the modular and systematic assembly of polysubstituted 3-fluoropyrroles. This synthesis provides an alternative and highly convergent strategy for the generation of these chemically and biologically important units.

Regio- and chemoselective intermolecular hydroamination of allyl imines for the synthesis of 1,2-diamines

Ickes, Andrew R.,Ensign, Seth C.,Gupta, Anil K.,Hull, Kami L.

supporting information, p. 11256 - 11259 (2014/09/29)

The synthesis of 1,2-diamines via a Rh-catalyzed intermolecular hydroamination of N-allyl imines with cyclic amines is presented. Coordinating groups proximal to the olefin bind to the catalyst and promote the transformation. The reaction affords 1,2-diam

Enantioselective synthesis of 1-aryl-2-propenylamines: A new approach to a stereoselective synthesis of the Taxol side chain

Castagnolo, Daniele,Armaroli, Silvia,Corelli, Federico,Botta, Maurizio

, p. 941 - 949 (2007/10/03)

A variety of substituted 1-aryl-2-propenylamines of high enantiomeric purity were prepared via lipase-catalysed resolution of the corresponding racemates. (R)-1-Phenyl-2-propenylamine was further synthesised into (2R,3S)-3-benzoylamino-2-hydroxy-3-phenylpropanoic acid methyl ester, the side chain of Taxol.

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