Chemical Properties of Bensulide (CAS 741-58-2)

Bensulide

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InChI
InChI=1S/C14H24NO4PS3/c1-12(2)18-20(21,19-13(3)4)22-11-10-15-23(16,17)14-8-6-5-7-9-14/h5-9,12-13,15H,10-11H2,1-4H3
InChI Key
RRNIZKPFKNDSRS-UHFFFAOYSA-N
Formula
C14H24NO4PS3
SMILES
CC(C)OP(=S)(OC(C)C)SCCNS(=O)(=O)c1ccccc1
Molecular Weight1
397.51
CAS
741-58-2
Other Names
  • Betasan
  • Disan
  • Disan (pesticide)
  • N-(2-Mercaptoethyl)benzenesulfonamide S-(O,O-diisopropyl phosphorodithioate)
  • N-[2-(O,O-Diisopropyldithiophosphoryl)ethyl]benzenesulfonamide
  • O,O-Diisopropyl 2-(benzenesulfonamido)ethyl dithiophosphate
  • O,O-Diisopropyl S-(2-benzenesulfonylaminoethyl) phosphorodithioate
  • Phosphorodithioic acid, O,O-bis(1-methylethyl) S-[2-[(phenylsulfonyl)amino]ethyl] ester
  • Phosphorodithioic acid, O,O-diisopropyl ester, S-ester with N-(2-mercaptoethyl)benzenesulfonamide
  • Prefar
  • R 4461
  • S-«beta»-(Benzenesulfonamido)ethyl O,O-diisopropyl dithiophosphate
  • S-«beta»-(Benzenesulfonamido)ethyl O,O-diisopropyl dithiophosphate
  • SAP
  • SAP (herbicide)
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Physical Properties

Property Value Unit Source
log10WS [-4.20; -4.20]   Show Hide
log10WS -4.20 Aq. Sol...
log10WS -4.20 Estimat...
logPoct/wat 3.773 Crippen Calculated Property
McVol 287.330 ml/mol McGowan Calculated Property
Inp [2728.00; 2728.00]   Show Hide
Inp 2728.00 NIST
Inp 2728.00 NIST
Inp 2728.00 NIST
Tfus [307.55; 311.57] K Show Hide
Tfus 307.55 K Aq. Sol...
Tfus 311.57 ± 0.20 K NIST

Similar Compounds

vasicinone. 3-Ethyl-2-isopropyl-3,5-dimethyl-1,4,2-diazaphosphorine-2-oxide. 12-O-Methylcarnosol. Hexahydro-3,3,5-trimethyl-2-p-tolyl-1,4,2-diazaphosphorine-2-oxide. Oxycodone, trimethylsilyl ether. (E)-Eruciflorine. Nalbuphine, O,O,O-tris(trimethylsilyl) deriv.. Eruciflorine. Naloxone, bis(trimethylsilyl) ether. Oxymorphone. Adenosine, N-(trimethylsilyl)-2',3'-bis-O-(trimethylsilyl)-, 5'-[bis(trimethylsilyl) phosphate]. Glyceollin III, TMS. Oxycodone. Morphinan-6-one, 4,5-epoxy-3,14-dihydroxy-17-(2-propenyl)-, (5«alpha»)-. Senecionine, 12-acetyl.

Find more compounds similar to Bensulide.

Sources

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