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(Top)
 


1 See also  





2 References  














4-Bromo-3,5-dimethoxyamphetamine






تۆرکجه
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Srpskohrvatski / српскохрватски
 

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From Wikipedia, the free encyclopedia
 


4-Bromo-3,5-dimethoxyamphetamine
Names
Preferred IUPAC name

1-(4-Bromo-3,5-dimethoxyphenyl)propan-2-amine

Other names

4-Bromo-3,5-dimethoxyamphetamine
2-(4-Bromo-3,5-dimethoxy-phenyl)-1-methyl-ethylamine
2-(4-Bromo-3,5-dimethoxyphenyl)ethan-1-methyl-amine

Identifiers

CAS Number

3D model (JSmol)

  • Interactive image
  • ChEMBL
    ChemSpider

    PubChem CID

    UNII

    CompTox Dashboard (EPA)

    • InChI=1S/C11H16BrNO2/c1-7(13)4-8-5-9(14-2)11(12)10(6-8)15-3/h5-7H,4,13H2,1-3H3 checkY

      Key: FAVLJTSHWBEOMA-UHFFFAOYSA-N checkY

    • InChI=1/C11H16BrNO2/c1-7(13)4-8-5-9(14-2)11(12)10(6-8)15-3/h5-7H,4,13H2,1-3H3

      Key: FAVLJTSHWBEOMA-UHFFFAOYAG

    • C1=C(C(=C(C=C1CC(C)N)OC)Br)OC

    • Brc1c(OC)cc(cc1OC)CC(N)C

    Properties

    Chemical formula

    C11H17BrNO2
    Molar mass 275.166 g·mol−1

    Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

    ☒N verify (what is checkY☒N ?)

    Infobox references

    4-Bromo-3,5-dimethoxyamphetamine is a lesser-known psychedelic drug and a substituted amphetamine. It was first synthesized by Alexander Shulgin. In his book PiHKAL, the dosage range is listed as 4–10 mg and the duration is listed as 8–12 hours.[1] It produces analgesia, numbness, and reduction of physical feeling. Very little data exists about its pharmacological properties, metabolism, and toxicity.

    See also[edit]

    References[edit]

    1. ^ "4-Bromo-3,5-dimethoxyamphetamine Entry in PiHKAL". Archived from the original on 2007-06-06. Retrieved 2007-03-28.
  • t
  • e

  • Retrieved from "https://en.wikipedia.org/w/index.php?title=4-Bromo-3,5-dimethoxyamphetamine&oldid=1203427257"

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