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[ CAS No. 786709-32-8 ] {[proInfo.proName]}

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Chemical Structure| 786709-32-8
Chemical Structure| 786709-32-8
Structure of 786709-32-8 * Storage: {[proInfo.prStorage]}
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Product Details of [ 786709-32-8 ]

CAS No. :786709-32-8 MDL No. :MFCD18825657
Formula : C10H15NO3S Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 229.30 Pubchem ID :-
Synonyms :

Safety of [ 786709-32-8 ]

Signal Word: Class:N/A
Precautionary Statements: UN#:N/A
Hazard Statements: Packing Group:N/A

Application In Synthesis of [ 786709-32-8 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 786709-32-8 ]

[ 786709-32-8 ] Synthesis Path-Downstream   1~21

  • 1
  • [ 35320-23-1 ]
  • [ 98-59-9 ]
  • [ 786709-32-8 ]
YieldReaction ConditionsOperation in experiment
With pyridine
  • 2
  • [ 786709-32-8 ]
  • [ 177971-32-3 ]
YieldReaction ConditionsOperation in experiment
With potassium carbonate In acetone
  • 3
  • (Z)-(R)-4-(Toluene-4-sulfonylamino)-pent-2-ene-1-sulfinic acid methyl ester [ No CAS ]
  • [ 786709-32-8 ]
YieldReaction ConditionsOperation in experiment
Stage #1: (Z)-(R)-4-(Toluene-4-sulfonylamino)-pent-2-ene-1-sulfinic acid methyl ester With ozone In methanol at -78℃; for 0.75h; Stage #2: With sodium tetrahydroborate In methanol at -78 - 20℃;
  • 4
  • (Z)-(2S,5R)-5-(Toluene-4-sulfonylamino)-hex-3-ene-2-sulfinic acid methyl ester [ No CAS ]
  • [ 786709-32-8 ]
YieldReaction ConditionsOperation in experiment
Stage #1: (Z)-(2S,5R)-5-(Toluene-4-sulfonylamino)-hex-3-ene-2-sulfinic acid methyl ester With ozone In methanol at -78℃; for 0.75h; Stage #2: With sodium tetrahydroborate In methanol at -78 - 20℃;
  • 5
  • [ 4104-47-6 ]
  • [ 786709-32-8 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1.1: (R)-2,2'-isopropylidenebis(4-phenyl-2-oxazoline); Cu(OTf)2 / CH2Cl2 / 22 h / -85 °C 2.1: 0.5 h / 20 °C 3.1: O3 / methanol / 0.75 h / -78 °C 3.2: NaBH4 / methanol / -78 - 20 °C
Multi-step reaction with 3 steps 1.1: 68 percent / (R)-2,2'-isopropylidenebis(4-phenyl-2-oxazoline); Cu(OTf)2 / CH2Cl2 / 25 h / -85 °C 2.1: 0.5 h / 20 °C 3.1: O3 / methanol / 0.75 h / -78 °C 3.2: NaBH4 / methanol / -78 - 20 °C
  • 6
  • (1S,3R)-3,6-dihydro-3-methyl-2-tosyl-1λ4,2-thiazine 1-oxide [ No CAS ]
  • [ 786709-32-8 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1.1: 0.5 h / 20 °C 2.1: O3 / methanol / 0.75 h / -78 °C 2.2: NaBH4 / methanol / -78 - 20 °C
  • 7
  • [ 786709-29-3 ]
  • [ 786709-32-8 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1.1: 0.5 h / 20 °C 2.1: O3 / methanol / 0.75 h / -78 °C 2.2: NaBH4 / methanol / -78 - 20 °C
  • 8
  • [ 786709-32-8 ]
  • [ 214190-58-6 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: K2CO3 / acetone 2: CuI / diethyl ether
  • 9
  • [ 786709-32-8 ]
  • N-[2-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-4-methyl-N-((R)-1-methyl-dec-9-enyl)-benzenesulfonamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1: K2CO3 / acetone 2: CuI / diethyl ether 3: NaH
  • 10
  • 1-(1-phenylvinyl)hexahydrothiopyrylium tetraphenylborate [ No CAS ]
  • [ 786709-32-8 ]
  • (+)-(3R,5S)-3-methyl-5-phenyl-4-tosylmorpholine [ No CAS ]
YieldReaction ConditionsOperation in experiment
72% With caesium carbonate In dichloromethane at 20℃; for 6h; regioselective reaction;
  • 11
  • 1-(1-phenylvinyl)hexahydrothiopyrylium tetraphenylborate [ No CAS ]
  • [ 786709-32-8 ]
  • (+)-(3R,5S)-3-methyl-5-phenyl-4-tosylmorpholine [ No CAS ]
  • C18H21NO3S [ No CAS ]
  • (2S,5R)-trans-5-methyl-4-(4-methylbenzenesulfonyl)-2-phenylmorpholine [ No CAS ]
YieldReaction ConditionsOperation in experiment
1: 31% 2: 14% With 1,8-diazabicyclo[5.4.0]undec-7-ene In dichloromethane at 0 - 20℃; for 21h; Inert atmosphere; diastereoselective reaction;
  • 12
  • [ 1590449-58-3 ]
  • [ 786709-32-8 ]
  • C32H38N2O8S [ No CAS ]
YieldReaction ConditionsOperation in experiment
98 % de With silver trifluoromethanesulfonate In neat (no solvent) at 20℃; for 10h; Inert atmosphere; stereoselective reaction;
  • 13
  • [ 1590450-42-2 ]
  • [ 786709-32-8 ]
  • C32H37ClN2O8S [ No CAS ]
YieldReaction ConditionsOperation in experiment
96 % de With silver trifluoromethanesulfonate In neat (no solvent) at 20℃; for 10h; Inert atmosphere; stereoselective reaction;
  • 14
  • [ 786709-32-8 ]
  • (2S,5R)-trans-5-methyl-4-(4-methylbenzenesulfonyl)-2-phenylmorpholine [ No CAS ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 4 steps 1: silver trifluoromethanesulfonate / neat (no solvent) / 10 h / 20 °C / Inert atmosphere 2: lithium aluminium tetrahydride / tetrahydrofuran / 2 h / 0 °C / Inert atmosphere 3: triethylamine; dmap / dichloromethane / 10 h / 20 °C / Inert atmosphere 4: potassium carbonate / acetonitrile / 48 h / 20 °C / Inert atmosphere
  • 15
  • [ 786709-32-8 ]
  • (2S,5R)-trans-2-(4-chlorophenyl)-5-methyl-4-(4-methylbenzenesulfonyl)morpholine [ No CAS ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 4 steps 1: silver trifluoromethanesulfonate / neat (no solvent) / 10 h / 20 °C / Inert atmosphere 2: lithium aluminium tetrahydride / tetrahydrofuran / 2 h / 0 °C / Inert atmosphere 3: triethylamine; dmap / dichloromethane / 10 h / 20 °C / Inert atmosphere 4: potassium carbonate / acetonitrile / 48 h / 20 °C / Inert atmosphere
  • 16
  • [ 786709-32-8 ]
  • C18H22ClNO4S [ No CAS ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: silver trifluoromethanesulfonate / neat (no solvent) / 10 h / 20 °C / Inert atmosphere 2: lithium aluminium tetrahydride / tetrahydrofuran / 2 h / 0 °C / Inert atmosphere
  • 17
  • [ 786709-32-8 ]
  • C25H28ClNO6S2 [ No CAS ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1: silver trifluoromethanesulfonate / neat (no solvent) / 10 h / 20 °C / Inert atmosphere 2: lithium aluminium tetrahydride / tetrahydrofuran / 2 h / 0 °C / Inert atmosphere 3: triethylamine; dmap / dichloromethane / 10 h / 20 °C / Inert atmosphere
  • 18
  • [ 786709-32-8 ]
  • C18H23NO4S [ No CAS ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: silver trifluoromethanesulfonate / neat (no solvent) / 10 h / 20 °C / Inert atmosphere 2: lithium aluminium tetrahydride / tetrahydrofuran / 2 h / 0 °C / Inert atmosphere
  • 19
  • [ 786709-32-8 ]
  • C25H29NO6S2 [ No CAS ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1: silver trifluoromethanesulfonate / neat (no solvent) / 10 h / 20 °C / Inert atmosphere 2: lithium aluminium tetrahydride / tetrahydrofuran / 2 h / 0 °C / Inert atmosphere 3: triethylamine; dmap / dichloromethane / 10 h / 20 °C / Inert atmosphere
  • 20
  • [ 932-87-6 ]
  • [ 786709-32-8 ]
  • (R)-N-(1-hydroxypropan-2-yl)-4-methyl-N-(phenylethynyl)benzenesulfonamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
32% With 1,10-Phenanthroline; copper(ll) sulfate pentahydrate; potassium carbonate In toluene at 80℃; for 12h; Inert atmosphere;
  • 21
  • [ 786709-32-8 ]
  • (R)-2-((4-methylphenyl)sulfonamido)propyl-(Z)-2-(1-methyl-2-oxoindolin-3-ylidene)-2-phenylacetate [ No CAS ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: potassium carbonate; 1,10-Phenanthroline; copper(ll) sulfate pentahydrate / toluene / 12 h / 80 °C / Inert atmosphere 2: zinc trifluoromethanesulfonate / 1,2-dichloro-ethane / 40 °C / Molecular sieve
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