4-Bromo-3,5-dimethoxyamphetamine

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	32156-34-6 ;
3D model (JSmol)	Interactive image; Interactive image;
ChEMBL	ChEMBL104362 ;
ChemSpider	180279 ;
PubChem CID	208044;
	InChI 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 Key: FAVLJTSHWBEOMA-UHFFFAOYSA-N ; 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;
	SMILES C1=C(C(=C(C=C1CC(C)N)OC)Br)OC; Brc1c(OC)cc(cc1OC)CC(N)C;
Properties
Chemical formula	C11H17NO2Br
Molar mass	274.154 g/mol
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	verify (what is ?)
	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 (Phenethylamines i Have Known And Loved), the dosage range is listed as 4–10 mg, and the duration listed as 8–12 hours. It produces analgesia, numbness and reduction of physical feeling. Very little data exists about its pharmacological properties, metabolism, and toxicity.

References

This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.