dimethylmyleran (CHEBI:67107)

ChEBI > Main

Main

ChEBI Ontology

Automatic Xrefs

Reactions

Pathways

Models

ChEBI Name	dimethylmyleran

ChEBI ID	CHEBI:67107

Definition	A methanesulfonate ester that is hexane-2,5-diol in which the hydrogens of the hydroxy groups are replaced by methanesulfonyl groups.

Stars	This entity has been manually annotated by the ChEBI Team.

Supplier Information

Download	Molfile XML SDF

more structures >>

Formula

C8H18O6S2

Net Charge

Average Mass

274.35500

Monoisotopic Mass

274.05448

InChI

InChI=1S/C8H18O6S2/c1-7(13-15(3,9)10)5-6-8(2)14-16(4,11)12/h7-8H,5-6H2,1-4H3

InChIKey

JDZNTUQRMDAIRO-UHFFFAOYSA-N

SMILES

CC(CCC(C)OS(C)(=O)=O)OS(C)(=O)=O

Roles Classification
Biological Role(s):	mutagen An agent that increases the frequency of mutations above the normal background level, usually by interacting directly with DNA and causing it damage, including base substitution. alkylating agent Highly reactive chemical that introduces alkyl radicals into biologically active molecules and thereby prevents their proper functioning. It could be used as an antineoplastic agent, but it might be very toxic, with carcinogenic, mutagenic, teratogenic, and immunosuppressant actions. It could also be used as a component of poison gases.

ChEBI Ontology
Outgoing	dimethylmyleran (CHEBI:67107) has role alkylating agent (CHEBI:22333) dimethylmyleran (CHEBI:67107) has role mutagen (CHEBI:25435) dimethylmyleran (CHEBI:67107) is a methanesulfonate ester (CHEBI:25223)

IUPAC Name

hexane-2,5-diyl dimethanesulfonate

Synonyms	Sources
1,4-bis(methylsulfonyloxy)-1,4-dimethylbutane	ChemIDplus
1,4-dimethanesulfonoxy-1,4-dimethylbutane	ChemIDplus
1,4-dimethylbusulfan	ChEBI
1,4-dimethylmyleran	ChEBI
2,5-dimethanesulfomyloxyhexane	ChemIDplus
2,5-hexanediol dimesylate	ChEBI
2,5-hexanediol dimethylsulfonate	ChemIDplus
dimethylbusulfan	ChemIDplus
DMM	ChemIDplus

Citation	Type	Source
3800321	PubMed citation	Europe PMC

Last Modified

10 August 2012