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Details

Stereochemistry RACEMIC
Molecular Formula C19H22ClNO2
Molecular Weight 331.836
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DIFENCLOXAZINE

SMILES

ClC1=CC=C(C=C1)C(OCCN2CCOCC2)C3=CC=CC=C3

InChI

InChIKey=CQDJBGPGXJWZTD-UHFFFAOYSA-N
InChI=1S/C19H22ClNO2/c20-18-8-6-17(7-9-18)19(16-4-2-1-3-5-16)23-15-12-21-10-13-22-14-11-21/h1-9,19H,10-15H2

HIDE SMILES / InChI

Molecular Formula C19H22ClNO2
Molecular Weight 331.836
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Substance Class Chemical
Created
by admin
on Fri Dec 15 16:39:08 GMT 2023
Edited
by admin
on Fri Dec 15 16:39:08 GMT 2023
Record UNII
M277CV2CL8
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DIFENCLOXAZINE
INN  
INN  
Official Name English
.BETA.-MORPHOLINOETHYL PHENYL-P-CHLOROPHENYLMETHYL ETHER
Common Name English
4-(2-.ALPHA.-PHENYL-P-CHLOROBENZYLOXYETHYL)MORPHOLINE
Common Name English
DIPHENCHLOXAZINE
Common Name English
MORPHOLINE, 4-(2-((4-CHLOROPHENYL)PHENYLMETHOXY)ETHYL)-
Systematic Name English
4-(2-PHENYL-P-CHLOROPHENYLMETHOXYETHYL)MORPHOLINE
Common Name English
4-(2-(P-CHLORO-.ALPHA.-PHENYLBENZYLOXY)ETHYL)MORPHOLINE
Common Name English
(P-CHLOROPHENYL)PHENYL-.BETA.-MORPHOLINOETHOXYMETHANE
Common Name English
difencloxazine [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29756
Created by admin on Fri Dec 15 16:39:08 GMT 2023 , Edited by admin on Fri Dec 15 16:39:08 GMT 2023
Code System Code Type Description
EVMPD
SUB07120MIG
Created by admin on Fri Dec 15 16:39:08 GMT 2023 , Edited by admin on Fri Dec 15 16:39:08 GMT 2023
PRIMARY
SMS_ID
100000083153
Created by admin on Fri Dec 15 16:39:08 GMT 2023 , Edited by admin on Fri Dec 15 16:39:08 GMT 2023
PRIMARY
FDA UNII
M277CV2CL8
Created by admin on Fri Dec 15 16:39:08 GMT 2023 , Edited by admin on Fri Dec 15 16:39:08 GMT 2023
PRIMARY
INN
1150
Created by admin on Fri Dec 15 16:39:08 GMT 2023 , Edited by admin on Fri Dec 15 16:39:08 GMT 2023
PRIMARY
ChEMBL
CHEMBL2110843
Created by admin on Fri Dec 15 16:39:08 GMT 2023 , Edited by admin on Fri Dec 15 16:39:08 GMT 2023
PRIMARY
EPA CompTox
DTXSID90863580
Created by admin on Fri Dec 15 16:39:08 GMT 2023 , Edited by admin on Fri Dec 15 16:39:08 GMT 2023
PRIMARY
PUBCHEM
9973981
Created by admin on Fri Dec 15 16:39:08 GMT 2023 , Edited by admin on Fri Dec 15 16:39:08 GMT 2023
PRIMARY
CAS
5617-26-5
Created by admin on Fri Dec 15 16:39:08 GMT 2023 , Edited by admin on Fri Dec 15 16:39:08 GMT 2023
PRIMARY
NCI_THESAURUS
C77253
Created by admin on Fri Dec 15 16:39:08 GMT 2023 , Edited by admin on Fri Dec 15 16:39:08 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY