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Chemical Structure| 96989-50-3 Chemical Structure| 96989-50-3

Structure of 96989-50-3

Chemical Structure| 96989-50-3

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Product Details of [ 96989-50-3 ]

CAS No. :96989-50-3
Formula : C11H8N2O2S
M.W : 232.26
SMILES Code : S=C(OC1=NC=CC=C1)OC2=NC=CC=C2
MDL No. :MFCD00074870
InChI Key :IKYOVSVBLHGFMA-UHFFFAOYSA-N
Pubchem ID :719784

Safety of [ 96989-50-3 ]

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

Application In Synthesis of [ 96989-50-3 ]

* 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 [ 96989-50-3 ]

[ 96989-50-3 ] Synthesis Path-Downstream   1~12

  • 1
  • [ 4214-57-7 ]
  • [ 96989-50-3 ]
  • [ 178929-37-8 ]
  • 2
  • [ 22802-67-1 ]
  • [ 96989-50-3 ]
  • [ 70751-84-7 ]
YieldReaction ConditionsOperation in experiment
In dichloromethane; PREPARATION 32.1 2-Methoxy-5-(5-methylsulfonyl-1H-tetrazol-1-yl)benzoic Acid According to the method of Tet. Let., 26, 1661 (1985), combine <strong>[22802-67-1]methyl 2-methoxy-5-aminobenzoate</strong> (0.5 g, 2.76 mmol) and di-2-pyridyl thionocarbonate (0.64 g, 2.76 mmol) in dichloromethane (10 mL). After 30 minutes, dilute the reaction mixture with dichloromethane and extract five times with water. Dry the organic layer over Na2SO4, filter, and concentrate in vacuo to give methyl 2-methoxy-5-isothiocyanatobenzoate: Rf=0.51 (silica gel, dichloromethane).
In dichloromethane; Treat a solution of 5-amino-2-methoxy-benzoic acid methyl ester (7.70 g, 42.5 mmol) and dichloromethane (50 mL) portionwise with a solution of di-2-pyridyl thionocarbonate (10.0 g, 43.1 mmol; Aldrich Chemical Company) and dichloromethane (70 mL) at room temperature under an argon atmosphere. After 3.5 hours, concentrate in vacuo and purify the residue by flash chromatography (silica gel, 5.5*17.8 cm) eluding with dichloromethane. Combine the appropriate fractions and concentrate to afford 5-isothiocyanato-2-methoxy-benzoic acid methyl ester (6,,9 g).
In dichloromethane; PREPARATION 32.1 2-Methoxy-5-(5-methylsulfonyl-1H-tetrazol-1-yl)benzoic acid According to the method of Tet. Let., 26, 1661 (1985), combine <strong>[22802-67-1]methyl 2-methoxy-5-aminobenzoate</strong> (0.5 g, 2.76 mmol) and di-2-pyridyl thionocarbonate (0.64 g, 2.76 mmol) in dichloromethane (10 mL). After 30 minutes, dilute the reaction mixture with dichloromethane and extract five times with water. Dry the organic layer over Na2SO4, filter, and concentrate in vacuo to give methyl 2-methoxy-5-isothiocyanatobenzoate: Rf=0.51 (silica gel, dichloromethane).
In dichloromethane; Treat a solution of 5-amino-2-methoxy-benzoic acid methyl ester (7.70 g, 42.5 mmol) and dichloromethane (50 mL) portionwise with a solution of di-2-pyridyl thionocarbonate (10.0 g, 43.1 mmol; Aldrich Chemical Company) and dichloromethane (70 mL) at room temperature under an argon atmosphere. After 3.5 hours, concentrate in vacuo and purify the residue by flash chromatography (silica gel, 5.5*17.8 cm) eluding with dichloromethane. Combine the appropriate fractions and concentrate to afford 5-isothiocyanato-2-methoxy-benzoic acid methyl ester (6.9 g).
In dichloromethane; Preparation 32.1 2-Methoxy-5-(5-methylsulfonyl-1H-tetrazol-1-yl)benzoic Acid According to the method of Tet. Let., 26, 1661 (1985), combine <strong>[22802-67-1]methyl 2-methoxy-5-aminobenzoate</strong> (0.5 g, 2.76 mmol) and di-2-pyridyl thionocarbonate (0.64 g, 2.76 mmol) in dichloromethane (10 mL). After 30 minutes, dilute the reaction mixture with dichloromethane and extract five times with water. Dry the organic layer over Na2SO4, filter, and concentrate in vacuo to give methyl 2-methoxy-5-isothiocyanatobenzoate: Rf=0.51 (silica gel, dichloromethane).
In dichloromethane; PREPARATION 32 2-Methoxy-5-(5-methylsulfonyltetrazol-1-yl)benzoic acid According to the method of Tet. Let., 26, 1661 (1985), combine <strong>[22802-67-1]methyl 2-methoxy-5-aminobenzoate</strong> (0.5 g, 2.76 mmol) and di-2-pyridyl thionocarbonate (0.64 g, 2.76 mmol) in dichloromethane (10 mL). After 30 minutes, dilute the reaction mixture with dichloromethane and extract five times with water. Dry the organic layer over Na2SO4, filter, and concentrate in vacuo to give methyl 2-methoxy-5-thioisocyanatobenzoate: Rf=0.51 (silica gel, dichloromethane).

  • 3
  • [ 123-75-1 ]
  • [ 29022-11-5 ]
  • [ 71989-31-6 ]
  • [ 71989-14-5 ]
  • [ 96989-50-3 ]
  • [ 64-19-7 ]
  • Nα-Fmoc-Nδ-(methyltrityl)-L-ornithine [ No CAS ]
  • [ 147290-11-7 ]
  • [ 1279698-76-8 ]
  • 4
  • [ 29022-11-5 ]
  • [ 593-51-1 ]
  • [ 71989-31-6 ]
  • [ 71989-14-5 ]
  • [ 96989-50-3 ]
  • [ 64-19-7 ]
  • Nα-Fmoc-Nδ-(methyltrityl)-L-ornithine [ No CAS ]
  • [ 147290-11-7 ]
  • [ 1279698-74-6 ]
  • 5
  • [ 29022-11-5 ]
  • [ 71989-31-6 ]
  • [ 71989-14-5 ]
  • [ 96989-50-3 ]
  • [ 64-19-7 ]
  • [ 124-40-3 ]
  • Nα-Fmoc-Nδ-(methyltrityl)-L-ornithine [ No CAS ]
  • [ 147290-11-7 ]
  • [ 1279698-75-7 ]
  • 6
  • [ 29022-11-5 ]
  • [ 71989-31-6 ]
  • [ 71989-14-5 ]
  • [ 96989-50-3 ]
  • [ 64-19-7 ]
  • Nα-Fmoc-Nδ-(methyltrityl)-L-ornithine [ No CAS ]
  • [ 147290-11-7 ]
  • [ 1279698-72-4 ]
  • 7
  • [ 29022-11-5 ]
  • [ 71989-31-6 ]
  • [ 71989-14-5 ]
  • [ 96989-50-3 ]
  • [ 64-19-7 ]
  • Nα-Fmoc-Nδ-(methyltrityl)-L-ornithine [ No CAS ]
  • [ 147290-11-7 ]
  • [ 1279698-73-5 ]
  • 8
  • [ 29022-11-5 ]
  • [ 71989-31-6 ]
  • [ 71989-14-5 ]
  • [ 96989-50-3 ]
  • [ 64-19-7 ]
  • Nα-Fmoc-Nδ-(methyltrityl)-L-ornithine [ No CAS ]
  • [ 147290-11-7 ]
  • [ 74-88-4 ]
  • [ 1279696-95-5 ]
  • 9
  • [ 29022-11-5 ]
  • [ 71989-31-6 ]
  • [ 71989-14-5 ]
  • [ 96989-50-3 ]
  • Nα-Fmoc-Nδ-(methyltrityl)-L-ornithine [ No CAS ]
  • [ 147290-11-7 ]
  • C42H52N8O7S [ No CAS ]
  • 10
  • [ 2632-65-7 ]
  • [ 96989-50-3 ]
  • [ 51317-64-7 ]
  • 11
  • [ 6274-22-2 ]
  • [ 96989-50-3 ]
  • [ 767329-08-8 ]
  • 12
  • [ 24835-08-3 ]
  • [ 96989-50-3 ]
  • 1-(isothiocyanatomethyl)-2-nitrobenzene [ No CAS ]
 

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