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Chemical Structure| 2386-53-0 Chemical Structure| 2386-53-0

Structure of 2386-53-0

Chemical Structure| 2386-53-0

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Product Details of [ 2386-53-0 ]

CAS No. :2386-53-0
Formula : C12H25NaO3S
M.W : 272.38
SMILES Code : CCCCCCCCCCCCS(=O)([O-])=O.[Na+]
MDL No. :MFCD00007527
InChI Key :DAJSVUQLFFJUSX-UHFFFAOYSA-M
Pubchem ID :23665726

Safety of [ 2386-53-0 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 2386-53-0 ]

* 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 [ 2386-53-0 ]

[ 2386-53-0 ] Synthesis Path-Downstream   1~35

  • 1
  • [ 1717-59-5 ]
  • [ 2386-53-0 ]
  • [ 75-46-7 ]
  • [ 120608-94-8 ]
  • 2
  • [ 3282-73-3 ]
  • [ 2386-53-0 ]
  • Dodecane-1-sulfonatedidodecyl-dimethyl-ammonium; [ No CAS ]
  • 3
  • [ 2386-53-0 ]
  • [ 112-52-7 ]
  • 4
  • [ 2386-53-0 ]
  • 1-dodecanesulfonyl fluoride [ No CAS ]
  • 5
  • [ 2386-53-0 ]
  • 4-n-hexadecyl-2,6-dimethylphenyl n-dodecanesulfonate [ No CAS ]
  • 6
  • [ 2386-53-0 ]
  • 2-(2-hydroxy-1-phenyl-ethyl)-isoquinolinium; dodecane-1-sulfonate [ No CAS ]
  • 7
  • [ 61546-03-0 ]
  • [ 2386-53-0 ]
  • [ 849900-41-0 ]
  • 10
  • trihydroxonitratodicopper(II) [ No CAS ]
  • [ 2386-53-0 ]
  • 2Cu(2+)*3OH(1-)*C12H25SO3(1-)=Cu2(OH)3(C12H25SO3) [ No CAS ]
  • 11
  • cis-diammineplatinum α-pyrrolidine tan nitrate*2H2O [ No CAS ]
  • [ 2386-53-0 ]
  • cis-diammineplatinum α-pyrrolidine tan dodecanesulfonate*5H2O [ No CAS ]
  • 12
  • ((platinum)4(NH3)8(α-pyrrolidonate)4)(NO3)6*2H2O [ No CAS ]
  • [ 2386-53-0 ]
  • [Pt4(NH3)8(αpyrrolidonato)4](n-C12H25SO3)6 [ No CAS ]
  • 13
  • scandium(III) chloride [ No CAS ]
  • [ 2386-53-0 ]
  • scandium dodecyl sulfate [ No CAS ]
  • 14
  • cis-diamminediaquaplatinum(II) dinitrate [ No CAS ]
  • [ 754-10-9 ]
  • [ 2386-53-0 ]
  • [Pt4(NH3)8(pivalamidato)4](n-C12H25SO3)5 [ No CAS ]
  • 15
  • copper(II) choride dihydrate [ No CAS ]
  • [ 2386-53-0 ]
  • 2C12H25SO3(1-)*Cu(2+)*4H2O=Cu(C12H25SO3)2*4H2O [ No CAS ]
  • 16
  • [ 2386-53-0 ]
  • cobalt(II) nitrate [ No CAS ]
  • Co(2+)*1.8OH(1-)*0.2C12H25OSO2(1-)=Co(OH)1.8(C12H25OSO2)0.2 [ No CAS ]
  • 17
  • [ 2386-53-0 ]
  • 2-phenylbenzo<1,2>quinolyzino<3,4,5,6-def>phenanthridinium tetrafluoroborate [ No CAS ]
  • [ 1172640-54-8 ]
  • 18
  • 2-phenyl-9-tetradecylbenzo[8,9]quinolizino[4,5,6,7-fed]phenanthridinylium chloride [ No CAS ]
  • [ 2386-53-0 ]
  • [ 1293990-67-6 ]
  • 19
  • [ 75-09-2 ]
  • [ 408496-42-4 ]
  • [ 1303609-88-2 ]
  • [ 2386-53-0 ]
  • [(C6H4C5H3(C6H13)N)2Ir((NC5H3CHCHC6H4NO2)2)](1+)*C12H25SO3(1-)*0.5CH2Cl2=C72H83N6O7SIr*0.5CH2Cl2 [ No CAS ]
  • 20
  • tetrakis(2-phenyl-4-methylpyridinato-N,C(2'))bis(μ-chloro)diiridium(III) [ No CAS ]
  • [ 116809-55-3 ]
  • [ 2386-53-0 ]
  • (C6H4C5H3(CH3)N)2Ir((NC5H3CHCHC6H4N(C2H5)2)2)(1+)*C12H25SO3(1-)=[(C6H4C5H3(CH3)N)2Ir((NC5H3CHCHC6H4N(C2H5)2)2)]C12H25SO3 [ No CAS ]
  • 21
  • [ 1119-94-4 ]
  • [ 2386-53-0 ]
  • [ 86291-55-6 ]
  • 22
  • [iridium(III)(μ-chloro)(2-phenylpyridine)2]2 [ No CAS ]
  • [ 2386-53-0 ]
  • 9-fullerifen-4,5-diazafluorene [ No CAS ]
  • (9-fulleriden-4,5-diazafluorene)bis(2-phenylpyrinato)iridium(III) dodecylsulfonate [ No CAS ]
  • 23
  • [iridium(III)(μ-chloro)(2-phenylpyridine)2]2 [ No CAS ]
  • [ 245-37-4 ]
  • [ 2386-53-0 ]
  • [ 1361061-34-8 ]
  • 24
  • [ 2386-53-0 ]
  • [ 1421060-63-0 ]
  • 25
  • [ 2386-53-0 ]
  • [ 1421060-53-8 ]
  • 26
  • [ 2386-53-0 ]
  • [ 682343-24-4 ]
  • 27
  • [ 2386-53-0 ]
  • [ 1174586-22-1 ]
  • 28
  • [ 2386-53-0 ]
  • 8-(4-dimethylaminophenyl)diazenyl-N,N-diethyl-10-phenylphenazin-10-ium-2-amine chloride [ No CAS ]
  • [ 1416251-66-5 ]
YieldReaction ConditionsOperation in experiment
Example 2; An ionic liquid (IL) was made to demonstrate the formation of a photoactive ionic liquid. A common dye, Janus Green B, was used as the cation of the IL. This cation was the light-sensitive component of the IL. Janus Green B absorbs in the visible range of the emission spectrum (by UV-Vis spectrophotometry). The anion used was dodecylsulfonate, which is a flexible long-chain alkyl that effectively lowers the melting point temperature. The Janus Green B-dodecylsulfonate IL was made by metathesis of the salt-forms of the dye Janus Green and sodium dodecyl sulfonate: NMR showed a 1:1.25 molar ratio of Janus Green B to dodecyl sulfonate. To determine purity, the silver nitrate (AgNO3) test was performed and a negative result for chlorine contamination was observed. The transition temperature for the IL was found to be below 100 C. (by differential scanning calorimetry), which falls within the classification of IL.
  • 29
  • [ 927690-63-9 ]
  • [ 2386-53-0 ]
  • C14H24N3(1+)*C12H25O3S(1-) [ No CAS ]
  • 30
  • cerium(III) chloride heptahydrate [ No CAS ]
  • [ 2386-53-0 ]
  • cerium(III) trislaurylsulfonate monohydrate [ No CAS ]
YieldReaction ConditionsOperation in experiment
In water; at 60℃; for 0.5h; General procedure: Cerium(III) trislaurylsulfonate monohydrate (Ce[SO3C12H25]3or denoted as Ce[LS]3) was synthesized according to a publishedprocedure as follows [39]. (i) 2.94 g of sodium laurylsulfonate (SLS,Aladdin, 98%) were added to 50 mL of distilled water and dissolved at 60 C in a water bath; (ii) 5.59 g of cerium(III) chloride hep-tahydrate (CeCl3·7H2O, Aladdin, 99%) were completely dissolvedin 50 mL of distilled water at room temperature and warmed up at 60 C in a water bath; (iii) after dissolution, the CeCl3solution wasadded under stirring, and the resulted slurry was stirred for 30 min.The white precipitate was filtered, recrystallized with hot distilledwater for 3 times, and dried in vacuum at room temperature (25 C) overnight.
  • 31
  • [ 2386-53-0 ]
  • iron(II) dodecylsulfate [ No CAS ]
  • 32
  • [ 112-52-7 ]
  • [ 2386-53-0 ]
  • 33
  • [ 2386-53-0 ]
  • [ 79917-90-1 ]
  • 1-butyl-3-methylimidazolium dodecylsulfonate [ No CAS ]
YieldReaction ConditionsOperation in experiment
In dichloromethane; at 20℃; for 15.0h; 1-Butyl-3-methylimidazolium chloride ([C4mim]Cl) was freshly prepared according to the procedures reported previously [14].1-Butyl-3-methylimidazolum dodecanesulfonate ([C4mim][C12SO3]) was obtained by ion exchange reaction of [C4mim]Cl and sodiumdodecylsulfonate. [C4mim]Cl and sodium 1-dodecanesulfonate were stirred in dichloromethane at room temperature for 15 h, and the precipitation was removed by filtration. Then the organic phase was washed with water until the water was chloride-free (tested by titration with AgNO3 from an acidic aqueous solution). The final product was dried in vacuum for 48 h at 55 C.
  • 34
  • [ 2386-53-0 ]
  • [ 819065-56-0 ]
  • C12H25O3S(1-)*Na(1+)*C18H8Cl2N6O4 [ No CAS ]
  • 35
  • [ 1071505-26-4 ]
  • [ 2386-53-0 ]
  • C12H25O3S(1-)*Na(1+)*C22H20N8O4*CH4 [ No CAS ]
 

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Technical Information

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