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[ CAS No. 31656-49-2 ]

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3d Animation Molecule Structure of 31656-49-2
Chemical Structure| 31656-49-2
Chemical Structure| 31656-49-2
Structure of 31656-49-2 * Storage: {[proInfo.prStorage]}
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Alternatived Products of [ 31656-49-2 ]

Product Details of [ 31656-49-2 ]

CAS No. :31656-49-2 MDL No. :MFCD14583105
Formula : C12H6N2 Boiling Point : -
Linear Structure Formula :- InChI Key :ZBFVJRBOKDTSMO-UHFFFAOYSA-N
M.W :178.19 Pubchem ID :11332803
Synonyms :

Safety of [ 31656-49-2 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P280-P305+P351+P338 UN#:N/A
Hazard Statements:H302 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 31656-49-2 ]

* 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 [ 31656-49-2 ]

[ 31656-49-2 ] Synthesis Path-Downstream   1~17

  • 1
  • [ 31656-49-2 ]
  • [ 5159-60-4 ]
  • 2
  • [ 31656-49-2 ]
  • [ 1141-38-4 ]
  • 3
  • 6-Bromo-2-naphthylazo phenyl sulfide [ No CAS ]
  • [ 10442-39-4 ]
  • [ 613-46-7 ]
  • [ 31656-49-2 ]
  • [ 129278-18-8 ]
  • 4
  • [ 74-90-8 ]
  • sodium-salt of/the/ 2-cyano-naphthalene-sulfonic acid-(6) [ No CAS ]
  • [ 31656-49-2 ]
  • [ 46289-40-1 ]
YieldReaction ConditionsOperation in experiment
at 335℃; for 1h; General procedure: Continued amide intermediate preparation examples. The reaction vessel (when the amide intermediate is boiled at atmospheric pressure, etc.) At or below the reaction temperature TB) or to keep the reactor in an open state (when the boiling point of the amide intermediate at atmospheric pressure is higher than the reaction temperature TB described below), stirring (600 r / min) The reaction temperature is changed to TB, After maintaining TD hours at the reaction temperature TB, the reaction vessel was closed and connected to a vacuum chestnut, So that the vacuum inside the reactor to 20-50mbar (according to the different types of nitrile and the corresponding adjustment) With distillate as a nitrile product. Calculate the yield of the nitrile product and sample the NMR spectrum and elemental analysis, To characterize the obtained nitrile product. The specific reaction conditions and characterization are shown in Tables A-5, A-6, A-7 and A-8. These characterization results show that the obtained nitrile product has a very high purity (99% or more)
With phosphorus pentoxide; at 335℃; under 15.0015 - 37.5038 Torr; for 1h; General procedure: Following the amide intermediate preparation example. The reaction vessel is closed (when the amide intermediate has a boiling point at atmospheric pressure, etc.At or below the reaction temperature TB described below) or keeping the reactor open (when the amide intermediate has a boiling point higher than the reaction temperature TB described below at normal pressure), stirring is continued (600 r/min). The reaction temperature was changed to TB. After TD hours at the reaction temperature TB, the reaction vessel was closed and connected to a vacuum pump so that the degree of vacuum in the reaction vessel reached 20-50 mbar (according to the type of nitrile product and corresponding adjustment) to distill off the reaction vessel. The product is a nitrile product. The yield of the nitrile product was calculated and sampled for nuclear magnetic proteomics and elemental analysis to characterize the nitrile product obtained. Specific reaction conditions and characterization results are shown in Tables A-5, A-6, A-7 and A-8 below. These characterization results show that the nitrile product obtained has an extremely high purity (above 99%). In these nitrile product preparation examples, 10 g of phosphorous pentoxide may be added as a catalyst to the reaction vessel at a time, optionally at the beginning of the reaction.
  • 8
  • [ 151-50-8 ]
  • potassium salt of/the/ naphthalene-disulfonic acid-(2.6) [ No CAS ]
  • [ 31656-49-2 ]
  • 9
  • [ 151-50-8 ]
  • sodium-<2-cyano-naphthalene sulfonate-(6)> [ No CAS ]
  • [ 31656-49-2 ]
  • 10
  • sodium-<2-cyano-naphthalene sulfonate-(6)> [ No CAS ]
  • potassium hexacyanoferrate(II) [ No CAS ]
  • [ 31656-49-2 ]
  • 11
  • [ 151-50-8 ]
  • sodium salt of/the/ naphthalene-disulfonic acid-(2.6) [ No CAS ]
  • [ 31656-49-2 ]
  • 12
  • [ 31656-49-2 ]
  • [ 5060-65-1 ]
YieldReaction ConditionsOperation in experiment
72.3% To A stirred solution of 3. 5 G (0. 02 mole) of 2, 6- DICYANONAPHTHALENE in 75 ML CH2Cl2 under N2 was added DIBAL (4. 26 g, 30 ML, 1 M solution in CYCLOHEXANE) in 10 min., after 15 min. stirring, it was heated at 45C for 45 min. The cooled reaction mixture (ice-bath) was decomposed with 2N H2S04 (50 ML) while stirring continued for 1 H, CH2Cl2 layer was separated, washed with water, NAHCOS, water and dried over NA2S04 and filtered and cone. in vac. triturated with hexane and filtered and dried to yield 2. 66 G (72. 3%) pale crystalline solid, M. P. 173-4C ; H-NMR (DMSO-D6) : 10. 18 (S, 1H), 10. 17 (S, 1H), 8. 57 (S, 2H), 8. 23 (D, 2H, J=8. 4HZ), 7. 96 (D, 2H, J=8. 4HZ) ; 13CNMR (DMSO-D6) : 192. 5, 135. 6, 134. 9, 133. 0, 130. 2, 123. 4 ; MS : M/E 184(M+).
  • 13
  • [ 34843-18-0 ]
  • [ 31656-49-2 ]
  • [ 83664-82-8 ]
  • 15
  • [ 46711-49-3 ]
  • [ 31656-49-2 ]
YieldReaction ConditionsOperation in experiment
With phosphorus pentoxide; under 15.0015 - 37.5038 Torr; for 1h;Heating; General procedure: Following the amide intermediate preparation example. The reaction vessel is closed (when the amide intermediate has a boiling point at normal pressure equal to or lower than the reaction temperature TB described below)Or keeping the reactor open (when the amide intermediate boiling point is higher than the reaction temperature TB described below),The stirring (600 r/min) is continued, the reaction temperature is changed to TB. After the reaction temperature TB is maintained for TD hours, the reaction vessel is closed and the vacuum pump is connected so that the degree of vacuum in the reaction vessel reaches 20-50 mbar (according to the type of nitrile product Differently adjusted accordingly) with distillate as nitrile product. The yield of the nitrile product was calculated and sampled for nuclear magnetic proteomics and elemental analysis to characterize the nitrile product obtained. Specific reaction conditions and characterization results are shown in Table A-5 and A-6 below.A-7 and A-8. These characterization results show that the nitrile product obtained has an extremely high purity (above 99%). In these nitrile product preparation examples, 10 g of phosphorous pentoxide may be added as a catalyst to the reaction vessel at a time, optionally at the beginning of the reaction.
  • 16
  • [ 1141-38-4 ]
  • [ 31656-49-2 ]
  • 17
  • [ 31656-49-2 ]
  • [ 1346242-75-8 ]
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