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Details

Stereochemistry RACEMIC
Molecular Formula C14H18F3NO.ClH
Molecular Weight 309.755
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of OXAFLOZANE HYDROCHLORIDE

SMILES

Cl.CC(C)N1CCOC(C1)C2=CC(=CC=C2)C(F)(F)F

InChI

InChIKey=XYYSVSLSSDHEGA-UHFFFAOYSA-N
InChI=1S/C14H18F3NO.ClH/c1-10(2)18-6-7-19-13(9-18)11-4-3-5-12(8-11)14(15,16)17;/h3-5,8,10,13H,6-7,9H2,1-2H3;1H

HIDE SMILES / InChI

Molecular Formula C14H18F3NO
Molecular Weight 273.294
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

Substance Class Chemical
Created
by admin
on Fri Dec 15 20:16:40 UTC 2023
Edited
by admin
on Fri Dec 15 20:16:40 UTC 2023
Record UNII
E10FW59D1I
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
OXAFLOZANE HYDROCHLORIDE
MART.   MI   WHO-DD  
Common Name English
1766CERM
Code English
((3-TRIFLUOROMETHYL)PHENYL)-4-ISOPROPYLTETRAHYDRO-1,4-OXAZINE HYDROCHLORIDE
Common Name English
OXAFLOZANE HYDROCHLORIDE [MI]
Common Name English
OXAFLOZANE HYDROCHLORIDE [MART.]
Common Name English
CONFLICTAN
Brand Name English
MORPHOLINE, 4-(1-METHYLETHYL)-2-(3-(TRIFLUOROMETHYL)PHENYL)-, HYDROCHLORIDE (1:1)
Systematic Name English
CERM-1766
Code English
Oxaflozane hydrochloride [WHO-DD]
Common Name English
NSC-315281
Code English
Code System Code Type Description
ECHA (EC/EINECS)
247-854-2
Created by admin on Fri Dec 15 20:16:40 UTC 2023 , Edited by admin on Fri Dec 15 20:16:40 UTC 2023
PRIMARY
NSC
315281
Created by admin on Fri Dec 15 20:16:40 UTC 2023 , Edited by admin on Fri Dec 15 20:16:40 UTC 2023
PRIMARY
MERCK INDEX
m861
Created by admin on Fri Dec 15 20:16:40 UTC 2023 , Edited by admin on Fri Dec 15 20:16:40 UTC 2023
PRIMARY Merck Index
FDA UNII
E10FW59D1I
Created by admin on Fri Dec 15 20:16:40 UTC 2023 , Edited by admin on Fri Dec 15 20:16:40 UTC 2023
PRIMARY
SMS_ID
100000085504
Created by admin on Fri Dec 15 20:16:40 UTC 2023 , Edited by admin on Fri Dec 15 20:16:40 UTC 2023
PRIMARY
CAS
26629-86-7
Created by admin on Fri Dec 15 20:16:40 UTC 2023 , Edited by admin on Fri Dec 15 20:16:40 UTC 2023
PRIMARY
EVMPD
SUB03560MIG
Created by admin on Fri Dec 15 20:16:40 UTC 2023 , Edited by admin on Fri Dec 15 20:16:40 UTC 2023
PRIMARY
MESH
C005357
Created by admin on Fri Dec 15 20:16:40 UTC 2023 , Edited by admin on Fri Dec 15 20:16:40 UTC 2023
PRIMARY
PUBCHEM
21124624
Created by admin on Fri Dec 15 20:16:40 UTC 2023 , Edited by admin on Fri Dec 15 20:16:40 UTC 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY