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Details

Stereochemistry ACHIRAL
Molecular Formula C21H18NO4.HO
Molecular Weight 365.3793
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CHELERYTHRINE HYDROXIDE

SMILES

[OH-].COC1=CC=C2C(C=[N+](C)C3=C2C=CC4=C3C=C5OCOC5=C4)=C1OC

InChI

InChIKey=YZYNINHQZLUUAW-UHFFFAOYSA-M
InChI=1S/C21H18NO4.H2O/c1-22-10-16-13(6-7-17(23-2)21(16)24-3)14-5-4-12-8-18-19(26-11-25-18)9-15(12)20(14)22;/h4-10H,11H2,1-3H3;1H2/q+1;/p-1

HIDE SMILES / InChI

Molecular Formula HO
Molecular Weight 17.0073
Charge -1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C21H18NO4
Molecular Weight 348.3719
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 10:58:47 UTC 2023
Edited
by admin
on Sat Dec 16 10:58:47 UTC 2023
Record UNII
65ML87R6OI
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CHELERYTHRINE HYDROXIDE
Common Name English
HELLERITRINE HYDROXIDE
Common Name English
CHELERYTHRINIUM HYDROXIDE
Common Name English
TODDALINE HYDROXIDE
Common Name English
(1,3)BENZODIOXOLO(5,6-C)PHENANTHRIDINIUM, 1,2-DIMETHOXY-12-METHYL-, HYDROXIDE (1:1)
Systematic Name English
NSC-76023
Code English
(1,3)BENZODIOXOLO(5,6-C)PHENANTHRIDINIUM, 1,2-DIMETHOXY-12-METHYL-, HYDROXIDE
Systematic Name English
TODDALIN HYDROXIDE
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID60963940
Created by admin on Sat Dec 16 10:58:47 UTC 2023 , Edited by admin on Sat Dec 16 10:58:47 UTC 2023
PRIMARY
PUBCHEM
5351594
Created by admin on Sat Dec 16 10:58:47 UTC 2023 , Edited by admin on Sat Dec 16 10:58:47 UTC 2023
PRIMARY
NSC
76023
Created by admin on Sat Dec 16 10:58:47 UTC 2023 , Edited by admin on Sat Dec 16 10:58:47 UTC 2023
PRIMARY
FDA UNII
65ML87R6OI
Created by admin on Sat Dec 16 10:58:47 UTC 2023 , Edited by admin on Sat Dec 16 10:58:47 UTC 2023
PRIMARY
CAS
478-03-5
Created by admin on Sat Dec 16 10:58:47 UTC 2023 , Edited by admin on Sat Dec 16 10:58:47 UTC 2023
PRIMARY