U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C7H16O4S2
Molecular Weight 228.33
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SULFONMETHANE

SMILES

CCS(=O)(=O)C(C)(C)S(=O)(=O)CC

InChI

InChIKey=CESKLHVYGRFMFP-UHFFFAOYSA-N
InChI=1S/C7H16O4S2/c1-5-12(8,9)7(3,4)13(10,11)6-2/h5-6H2,1-4H3

HIDE SMILES / InChI
Sulfonmethane (also known as acetone diethylsulfone) was discovered as a hypnotic drug. Sulfonmethane was to be one of Bayer’s first profitable pharmaceutical products. It retained its popularity until the introduction of the more rapidly acting barbiturates rendered it obsolete. Now is used newer and safer sedatives.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
PubMed

PubMed

TitleDatePubMed
The history of barbiturates a century after their clinical introduction.
2005 Dec
Name Type Language
SULFONMETHANE
MI  
Common Name English
2,2-BIS(ETHYLSULFONYL)PROPANE
Systematic Name English
NSC-26248
Code English
DIETHYLSULFONDIMETHYLMETHANE
Common Name English
ACETONE DIETHYLSULPHONE
Systematic Name English
ACETONE, BIS(ETHYL SULPHONE)
Common Name English
SULPHONALUM [HPUS]
Common Name English
SULPHONALUM
HPUS  
Common Name English
SULFONMETHANE [MI]
Common Name English
SULPHONAL
Common Name English
ACETONE, BIS(ETHYL SULFONE)
Common Name English
ACETONE DIETHYLSULFONE
Systematic Name English
SULFONAL
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29756
Created by admin on Fri Dec 15 15:50:34 UTC 2023 , Edited by admin on Fri Dec 15 15:50:34 UTC 2023
DEA NO. 2610
Created by admin on Fri Dec 15 15:50:34 UTC 2023 , Edited by admin on Fri Dec 15 15:50:34 UTC 2023
Code System Code Type Description
PUBCHEM
8262
Created by admin on Fri Dec 15 15:50:34 UTC 2023 , Edited by admin on Fri Dec 15 15:50:34 UTC 2023
PRIMARY
ECHA (EC/EINECS)
204-074-7
Created by admin on Fri Dec 15 15:50:34 UTC 2023 , Edited by admin on Fri Dec 15 15:50:34 UTC 2023
PRIMARY
MESH
C058436
Created by admin on Fri Dec 15 15:50:34 UTC 2023 , Edited by admin on Fri Dec 15 15:50:34 UTC 2023
PRIMARY
RXCUI
2534463
Created by admin on Fri Dec 15 15:50:34 UTC 2023 , Edited by admin on Fri Dec 15 15:50:34 UTC 2023
PRIMARY
DAILYMED
W00D22B592
Created by admin on Fri Dec 15 15:50:34 UTC 2023 , Edited by admin on Fri Dec 15 15:50:34 UTC 2023
PRIMARY
SMS_ID
100000136014
Created by admin on Fri Dec 15 15:50:34 UTC 2023 , Edited by admin on Fri Dec 15 15:50:34 UTC 2023
PRIMARY
NCI_THESAURUS
C90943
Created by admin on Fri Dec 15 15:50:34 UTC 2023 , Edited by admin on Fri Dec 15 15:50:34 UTC 2023
PRIMARY
FDA UNII
W00D22B592
Created by admin on Fri Dec 15 15:50:34 UTC 2023 , Edited by admin on Fri Dec 15 15:50:34 UTC 2023
PRIMARY
MERCK INDEX
m10360
Created by admin on Fri Dec 15 15:50:34 UTC 2023 , Edited by admin on Fri Dec 15 15:50:34 UTC 2023
PRIMARY Merck Index
NSC
26248
Created by admin on Fri Dec 15 15:50:34 UTC 2023 , Edited by admin on Fri Dec 15 15:50:34 UTC 2023
PRIMARY
EVMPD
SUB72970
Created by admin on Fri Dec 15 15:50:34 UTC 2023 , Edited by admin on Fri Dec 15 15:50:34 UTC 2023
PRIMARY
WIKIPEDIA
SULFONMETHANE
Created by admin on Fri Dec 15 15:50:34 UTC 2023 , Edited by admin on Fri Dec 15 15:50:34 UTC 2023
PRIMARY
ChEMBL
CHEMBL2103932
Created by admin on Fri Dec 15 15:50:34 UTC 2023 , Edited by admin on Fri Dec 15 15:50:34 UTC 2023
PRIMARY
CAS
115-24-2
Created by admin on Fri Dec 15 15:50:34 UTC 2023 , Edited by admin on Fri Dec 15 15:50:34 UTC 2023
PRIMARY
EPA CompTox
DTXSID3048574
Created by admin on Fri Dec 15 15:50:34 UTC 2023 , Edited by admin on Fri Dec 15 15:50:34 UTC 2023
PRIMARY