69232-78-6 Usage
Family
3,4-Methylenedioxyphenethylamine
Psychoactive properties
Yes
Entheogenic properties
Yes
Recreational use
Hallucinogenic effects, such as visual and auditory hallucinations, altered perception of time, and changes in mood
Chemical structure
Contains a benzodioxole ring, two methoxy substituents, and a 2-methoxypropyl side chain
Legal status
Illegal in many countries
Safety and long-term effects
Not well understood
Check Digit Verification of cas no
The CAS Registry Mumber 69232-78-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,2,3 and 2 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 69232-78:
(7*6)+(6*9)+(5*2)+(4*3)+(3*2)+(2*7)+(1*8)=146
146 % 10 = 6
So 69232-78-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H18O5/c1-8(14-2)5-9-6-10-12(18-7-17-10)13(16-4)11(9)15-3/h6,8H,5,7H2,1-4H3
69232-78-6Relevant academic research and scientific papers
Photon-Induced Reactions: Part V - Photochemical and Chemical Oxidation Products of Dillapiole and Isodillapiole
Walia, S.,Dureja, P.,Mukerjee, S. K.
, p. 147 - 150 (2007/10/02)
Several photometabolites of dillapiole (1), obtained by irradiating it in methanol have been identified as isodillapiole (2), dihydrodillapiole (3), 1-cyclopropyl-2,3-dimethoxy-4,5-methylenedioxybenzene (4), dillaldehyde (7) and two new methanol adducts (5) and (6).Isodillapiole (2) under the same conditions furnishes 5, 6 and 7.Dye-sensitized photooxidation of 1 gives, besides the aldehydes 7 and 8, dihydroxydillapiole (11).For comparison, KMnO4 oxidation of 1 has also been investigated in detail.
