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[ CAS No. 4922-51-4 ] {[proInfo.proName]}

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Chemical Structure| 4922-51-4
Chemical Structure| 4922-51-4
Structure of 4922-51-4 * Storage: {[proInfo.prStorage]}
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Product Details of [ 4922-51-4 ]

CAS No. :4922-51-4 MDL No. :MFCD07643239
Formula : C8H8N4 Boiling Point : -
Linear Structure Formula :- InChI Key :KTEQHOVTBRZQPC-UHFFFAOYSA-N
M.W : 160.18 Pubchem ID :3052732
Synonyms :

Safety of [ 4922-51-4 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P280 UN#:N/A
Hazard Statements:H302-H317 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 4922-51-4 ]

* 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 [ 4922-51-4 ]

[ 4922-51-4 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 63273-23-4 ]
  • [ 4922-51-4 ]
  • (3Z)-3-[4-(1H-1,2,4-triazol-3-yl)anilino]methylene}-1,3-dihydro-2H-indol-2-one [ No CAS ]
YieldReaction ConditionsOperation in experiment
EXAMPLE 6 Preparation of (3Z)-3-[4-(1H-1,2,4-triazol-3-yl)anilino]methylene}-1,3-dihydro-2H-indol-2-one Prepared in an analogous manner to Example 1 using one equivalent of <strong>[4922-51-4]4-(1H-1,2,4-triazol-3-yl)aniline</strong> in place of 5-aminobenzimidazolone. 1H NMR (400 MHz, d6-DMSO) delta14.32 (s, 1H, exchangeable); 14.05 (s, 1H, exchangeable); 10.82 (m, 1H); 10.54 (m, 1H); 8.64 (m, 1H); 8.60 (s, 1H, exchangeable); 8.00 (m, 2H); 7.63 (m, 1H); 7.47 (m, 1H); 7.03 (m, 1H); 6.94 (m, 1H); 6.85 (m, 1H). APCI MS (-ve) 302.
YieldReaction ConditionsOperation in experiment
By utilizing the suitable S-methyl-thioimidoylphosphonic acid monoethyl ester and substituting the following phenylamines: ... (c) 4-(3-chloro-4-amino-phenyl)-1-H-imidazole, (d) 4-(3-amino-phenyl)-1-H-imidazole, (e) 2-(4-amino-phenyl)-1-H-imidazole, (f) 3-(4-amino-phenyl)-pyrazole, or (g) 3-(4-amino-phenyl)-1,2,4-triazole
  • 3
  • [ 13734-34-4 ]
  • [ 4922-51-4 ]
  • C22H25N5O3 [ No CAS ]
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