Explore N,N-Me-2C-D | PiHKAL

ChemSpider 184245
PubChem 212478
Wikidata Q83049539

Shulgin Index See #19 2C-C · Table 5Page 342Row 23

Glennon, RA; Young, R; Jacyno, JM. Indolealkylamine and phenalkylamine hallucinogens: Effect of α-methyl and N-methyl substituents on behavioral activity. Biochem. Pharmacol., 1 Apr 1983, 32 (7), 1267–1273. 591 kB. https://doi.org/10.1016/0006-2952(83)90281-2 #DD-DOM

Ho, B; Tansey, LW; Balster, RL; An, R; McIsaac, WM; Harris, RT. Amphetamine analogs. II. Methylated phenethylamines. J. Med. Chem., 1 Jan 1970, 13 (1), 134–135. 278 kB. https://doi.org/10.1021/jm00295a034 #6

Brimblecombe, RW; Pinder, RM. Hallucinogenic agents, Wright-Scientechnica, Bristol, UK, 1 Jan 1975. 46.2 MB. #3.50

4C-D · 4C-DOM · ARIADNE · BL-3912 · α-Et-2C-D

N-Me-DOM · N-Methyl-DOM · BEATRICE

2C-P

DOE · DOET · HECATE

G · GANESHA

5-Ethoxy-2-methoxy-4-methylamphetamine · DOM-5ETO · IRIS

6-Me-DOM · JUNO

2,5-Diethoxy-4-methylphenethylamine · 2C-D-2,5-DiEtO · 2CD-25DIETO

2CE-5ETO

2,5-DNNA · N,N-Me-DOH

2,6-DNNA

3,5-DNNA · N,N-Me-3,5-DMA

BL-4041A · CHARMIAN · α-Me-DOM

DAPHNE

ELVIRA

2-Ethoxy-5-methoxy-4-methylamphetamine · DOM-2ETO · FLORENCE

2,4-DNNA

2155

25H-NPro

2C-IP

4,2,6-DOET · ψ-DOET

4-Butoxynorephedrine

homo-N,N-Me-2,5-DMPEA

homo-DOM

BO3MIP

β-HO-N-Pr-PMA

4C-2,3-DMPEA

N,N-Me-2,3-EMPEA

N,N-Me-DMA

6622

N,N-Me-3,4-EMPEA

N,N-Me-4,3-EMPEA

N-Me-DEPEA

DEA

β,N,N-Me-2,5-DMPEA

4,2,3-DOET

3,2,4-DOET

2,3,4-DOET

5,2,3-DOET

3,2,5-DOET

2,3,5-DOET

5,2,4-DOET

β,β-Me-2C-D

β-Me-DOM

2,4,5-DOET

4,3,5-DOET

3,4,5-DOET

6,2,3-DOET

3,2,6-DOET

2,3,6-DOET

2,4,6-DOET

4-Me-2,6-MEA

6-Me-2,4-DEPEA

2C-G-21

2C-G-12

3,4,6-Me-2,5-DMPEA

IPOMA

POMA

10025

10026

10028

ψ-2C-IP

DPR

DIP

10439

PhenMetEtrazine precursor

ψ-4C-D