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Details

Stereochemistry RACEMIC
Molecular Formula C15H22ClN.ClH
Molecular Weight 288.256
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DIDESMETHYLSIBUTRAMINE HYDROCHLORIDE

SMILES

Cl.CC(C)CC(N)C1(CCC1)C2=CC=C(Cl)C=C2

InChI

InChIKey=KHRVYINTXCWNRF-UHFFFAOYSA-N
InChI=1S/C15H22ClN.ClH/c1-11(2)10-14(17)15(8-3-9-15)12-4-6-13(16)7-5-12;/h4-7,11,14H,3,8-10,17H2,1-2H3;1H

HIDE SMILES / InChI

Molecular Formula C15H22ClN
Molecular Weight 251.795
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
PubMed

PubMed

TitleDatePubMed
Patents

Patents

Substance Class Chemical
Created
by admin
on Sat Dec 16 08:21:37 GMT 2023
Edited
by admin
on Sat Dec 16 08:21:37 GMT 2023
Record UNII
XJH8PK8XYH
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DIDESMETHYLSIBUTRAMINE HYDROCHLORIDE
Common Name English
1-(1-(4-CHLOROPHENYL)CYCLOBUTYL)-3-METHYLBUTYLAMINE HYDROCHLORIDE
Systematic Name English
CYCLOBUTANEMETHANAMINE, 1-(4-CHLOROPHENYL)-.ALPHA.-(2-METHYLPROPYL)-, HYDROCHLORIDE
Systematic Name English
BTS-54-505
Code English
CYCLOBUTANEMETHANAMINE, 1-(4-CHLOROPHENYL)-.ALPHA.-(2-METHYLPROPYL)-, HYDROCHLORIDE (1:1)
Systematic Name English
DIDEMETHYLSIBUTRAMINE HYDROCHLORIDE
Common Name English
(1-(1-(4-CHLOROPHENYL)CYCLOBUTYL)-3-METHYLBUTAN-1-YL)AMINE HYDROCHLORIDE
Systematic Name English
Code System Code Type Description
CAS
84484-78-6
Created by admin on Sat Dec 16 08:21:37 GMT 2023 , Edited by admin on Sat Dec 16 08:21:37 GMT 2023
PRIMARY
FDA UNII
XJH8PK8XYH
Created by admin on Sat Dec 16 08:21:37 GMT 2023 , Edited by admin on Sat Dec 16 08:21:37 GMT 2023
PRIMARY
PUBCHEM
134771
Created by admin on Sat Dec 16 08:21:37 GMT 2023 , Edited by admin on Sat Dec 16 08:21:37 GMT 2023
PRIMARY
EPA CompTox
DTXSID801004760
Created by admin on Sat Dec 16 08:21:37 GMT 2023 , Edited by admin on Sat Dec 16 08:21:37 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY