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[ CAS No. 55406-13-8 ]

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type HazMat fee
Excepted Quantity Free
Inaccessible (Haz class 6.1), Domestic USD 41.00
Inaccessible (Haz class 6.1), International USD 64.00
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 83.00
Accessible (Haz class 3, 4, 5 or 8), International USD 133.00
Chemical Structure| 55406-13-8
Chemical Structure| 55406-13-8
Structure of 55406-13-8 * Storage: {[proInfo.prStorage]}

Quality Control of [ 55406-13-8 ]

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Product Details of [ 55406-13-8 ]

CAS No. :55406-13-8 MDL No. :MFCD00052086
Formula : C6H5NS Boiling Point : 212.7°C at 760 mmHg
Linear Structure Formula :- InChI Key :N/A
M.W :123.18 g/mol Pubchem ID :-
Synonyms :

Safety of [ 55406-13-8 ]

Signal Word:Danger Class:6.1
Precautionary Statements:P261-P264-P270-P271-P280-P301+P310+P330-P302+P352+P312-P304+P340+P312-P363-P405-P501 UN#:3276
Hazard Statements:H301-H312-H332 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 55406-13-8 ]

  • Downstream synthetic route of [ 55406-13-8 ]

[ 55406-13-8 ] Synthesis Path-Downstream   1~15

  • 1
  • [ 16494-40-9 ]
  • [ 544-92-3 ]
  • [ 55406-13-8 ]
  • 3
  • [ 75-77-4 ]
  • [ 55406-13-8 ]
  • [ 198633-86-2 ]
YieldReaction ConditionsOperation in experiment
64% Example 44. 3-Methyl-5-(trimethylsilyl)thiophene-2-carbonitriIe (Scheme No.10, A). To a -780C stirred solution of freshly prepared LDA (2.17 g, 20.30 mmol) in THF (20 mL) was slowly added <strong>[55406-13-8]3-methylthiophene-2-carbonitrile</strong> (2.50 g, 20.30 mmol) in THF (10 mL) and the reaction was stirred at -78 0C for 5 minutes. To this anion was slowly added trimethylsilyl chloride (2.84 mL, 22.33 mmole) and the reaction stirred at -780C for 30 minutes. The ice bath was removed, warmed to room temperature and stirred an additional hour. The THF was removed' under reduced pressure at ambient temperature to yield a bright yellow oil. The crude compound was purified using flash chromatography (neutral activated alumina, 10:90 ether: hexanes) to give the title compound as a volatile, clear colorless oil (2.52 g, 64%). 1H NMR (300 MHz, DMSO-d6) δ 0.34 (s, 9H); 2.43 (s, 3H); 6.95 (s, IH). HPLC (Platform 3): 2.93 minutes, m/z (APCI) 237 M + 41.
  • 4
  • [ 55406-13-8 ]
  • [ 104-96-1 ]
  • 3-methyl-<i>N</i>-(4-methylsulfanyl-phenyl)-thiophene-2-carboxamidine [ No CAS ]
  • 6
  • [ 55406-13-8 ]
  • [ 107-15-3 ]
  • [ 127199-59-1 ]
  • 8
  • [ 55406-13-8 ]
  • [ 878649-98-0 ]
  • 9
  • [ 14345-97-2 ]
  • [ 557-21-1 ]
  • [ 55406-13-8 ]
  • 10
  • [ 55406-13-8 ]
  • [ 878650-22-7 ]
  • 11
  • [ 55406-13-8 ]
  • 5,6-dihydroxy-2-(3-methyl-thiophen-2-yl)-pyrimidine-4-carboxylic acid [ No CAS ]
  • 12
  • [ 55406-13-8 ]
  • [ 878650-11-4 ]
  • 13
  • [ 55406-13-8 ]
  • 1-(4-methylsulfanyl-phenyl)-2-(3-methyl-thiophen-2-yl)-4-trifluoromethyl-1<i>H</i>-imidazole [ No CAS ]
  • 14
  • [ 55406-13-8 ]
  • 1-(4-methylsulfanyl-phenyl)-2-(3-methyl-thiophen-2-yl)-4-trifluoromethyl-4,5-dihydro-1<i>H</i>-imidazol-4-ol [ No CAS ]
  • 15
  • [ 55406-13-8 ]
  • 1-(4-methanesulfonyl-phenyl)-2-(3-methyl-thiophen-2-yl)-4-trifluoromethyl-1<i>H</i>-imidazole [ No CAS ]
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