Misplaced Pages

Methylenedioxymethoxyethylamphetamine: Difference between revisions

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.
Browse history interactively← Previous editContent deleted Content addedVisualWikitext
Revision as of 07:41, 21 April 2012 editMSBOT (talk | contribs)13,809 editsm r2.7.3) (Robot: Adding fa:متیلن‌دی‌اکسی‌متوکسی‌اتیل‌آمفتامین← Previous edit Latest revision as of 20:53, 10 March 2024 edit undoInternetArchiveBot (talk | contribs)Bots, Pending changes reviewers5,386,108 edits Rescuing 1 sources and tagging 0 as dead.) #IABot (v2.0.9.5) (Maxim Masiutin - 17955 
(13 intermediate revisions by 12 users not shown)
Line 1: Line 1:
{{chembox {{chembox
| Verifiedfields = changed
⚫ | verifiedrevid = 379536713
| Watchedfields = changed
⚫ | verifiedrevid = 424728565
| Name=Methylenedioxymethoxyethyl{{shy}}amphetamine
| ImageFile = MDMEOET.png | ImageFile = MDMEOET.png
| ImageSize = 200px | ImageSize = 200px
| IUPACName = 1-(1,3-benzodioxol-5-yl)-''N''-(2-methoxyethyl)propan-2-amine | PIN = 1-(2''H''-1,3-Benzodioxol-5-yl)-''N''-(2-methoxyethyl)propan-2-amine
| OtherNames = | OtherNames =
| Section1 = {{Chembox Identifiers |Section1={{Chembox Identifiers
| CASNo_Ref = {{cascite|correct|??}}
| CASNo = 74698-44-5 | CASNo = 74698-44-5
| PubChem = | UNII = YPA4B5U3U8
| PubChem = 44719584
| SMILES = C1=C2C(=CC=C1CC(C)NCCOC)OCO2}}
| DTXSID = DTXSID10660371
⚫ | Section2 = {{Chembox Properties
| ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}}
| ChemSpiderID = 21106334
| SMILES = CC(Cc1ccc2c(c1)OCO2)NCCOC
| InChI = 1/C13H19NO3/c1-10(14-5-6-15-2)7-11-3-4-12-13(8-11)17-9-16-12/h3-4,8,10,14H,5-7,9H2,1-2H3
| InChIKey = LOZJEWOZOKSOKA-UHFFFAOYAB
| StdInChI_Ref = {{stdinchicite|changed|chemspider}}
| StdInChI = 1S/C13H19NO3/c1-10(14-5-6-15-2)7-11-3-4-12-13(8-11)17-9-16-12/h3-4,8,10,14H,5-7,9H2,1-2H3
| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}}
| StdInChIKey = LOZJEWOZOKSOKA-UHFFFAOYSA-N}}
⚫ |Section2={{Chembox Properties
| Formula = C<sub>13</sub>H<sub>19</sub>NO<sub>3</sub> | Formula = C<sub>13</sub>H<sub>19</sub>NO<sub>3</sub>
| MolarMass = 237.295 g/mol | MolarMass = 237.295 g/mol
Line 17: Line 31:
| BoilingPt = | BoilingPt =
| Solubility = }} | Solubility = }}
| Section3 = {{Chembox Hazards |Section3={{Chembox Hazards
| MainHazards = | MainHazards =
| FlashPt = | FlashPt =
| Autoignition = }} | AutoignitionPt = }}
}} }}


'''MDMEOET''', or 3,4-]enedioxy-N-]]], is a lesser-known ] and a ]. It is also the N-methoxyethyl analogue of ]. MDMEOET was first synthesized by ]. In his book '']'', the minimum dosage is listed as 180 ]. MDMEOET produces few to no effects. Very little data exists about the pharmacological properties, metabolism, and toxicity of MDMEOET. '''MDMEOET''', or 3,4-]enedioxy-N-]]], is a lesser-known ] and a ]. It is also the N-methoxyethyl analogue of ]. MDMEOET was first synthesized by ]. In his book '']'', the minimum dosage is listed as 180 ]. MDMEOET produces few to no effects. Very little data exists about the pharmacological properties, metabolism, and toxicity of MDMEOET.

==Legality==

===United Kingdom===
This substance is a Class A drug in the ].<ref>{{cite web | title = UK Misuse of Drugs act 2001 Amendment summary | url = http://isomerdesign.com/Cdsa/scheduleUK.php?schedule=1&ion=30&structure=C | accessdate = 12 March 2014 | publisher = Isomer Design | archive-date = 22 October 2017 | archive-url = https://web.archive.org/web/20171022085110/http://isomerdesign.com/Cdsa/scheduleUK.php?schedule=1&ion=30&structure=C | url-status = dead }}</ref>


== See also == == See also ==
Line 29: Line 48:
* ] * ]
* ] * ]

==References==
{{Reflist}}


== External links == == External links ==
Line 35: Line 57:


{{Methylenedioxyphenethylamines}} {{Methylenedioxyphenethylamines}}
{{PiHKAL}}


] ]
] ]


⚫ {{Psychoactive-stub}}


⚫ {{Psychoactive-stub}}
]

Latest revision as of 20:53, 10 March 2024

Methylenedioxymethoxyethyl­amphetamine
Names
Preferred IUPAC name 1-(2H-1,3-Benzodioxol-5-yl)-N-(2-methoxyethyl)propan-2-amine
Identifiers
CAS Number
3D model (JSmol)
ChemSpider
PubChem CID
UNII
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C13H19NO3/c1-10(14-5-6-15-2)7-11-3-4-12-13(8-11)17-9-16-12/h3-4,8,10,14H,5-7,9H2,1-2H3Key: LOZJEWOZOKSOKA-UHFFFAOYSA-N
  • InChI=1/C13H19NO3/c1-10(14-5-6-15-2)7-11-3-4-12-13(8-11)17-9-16-12/h3-4,8,10,14H,5-7,9H2,1-2H3Key: LOZJEWOZOKSOKA-UHFFFAOYAB
SMILES
  • CC(Cc1ccc2c(c1)OCO2)NCCOC
Properties
Chemical formula C13H19NO3
Molar mass 237.295 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). ☒N verify (what is  ?) Infobox references
Chemical compound

MDMEOET, or 3,4-methylenedioxy-N-methoxyethylamphetamine, is a lesser-known psychedelic drug and a substituted amphetamine. It is also the N-methoxyethyl analogue of MDA. MDMEOET was first synthesized by Alexander Shulgin. In his book PiHKAL (Phenethylamines i Have Known And Loved), the minimum dosage is listed as 180 mg. MDMEOET produces few to no effects. Very little data exists about the pharmacological properties, metabolism, and toxicity of MDMEOET.

Legality

United Kingdom

This substance is a Class A drug in the Drugs controlled by the UK Misuse of Drugs Act.

See also

References

  1. "UK Misuse of Drugs act 2001 Amendment summary". Isomer Design. Archived from the original on 22 October 2017. Retrieved 12 March 2014.

External links

Phenethylamines
Phenethylamines
Amphetamines
Phentermines
Cathinones
Phenylisobutylamines
Phenylalkylpyrrolidines
Catecholamines
(and close relatives)
Miscellaneous


Stub icon

This psychoactive drug-related article is a stub. You can help Misplaced Pages by expanding it.

Categories: