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[ CAS No. 3133-78-6 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 3133-78-6
Chemical Structure| 3133-78-6
Structure of 3133-78-6 * Storage: {[proInfo.prStorage]}

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Product Details of [ 3133-78-6 ]

CAS No. :3133-78-6 MDL No. :MFCD01830305
Formula : C10H8O2S Boiling Point : No data available
Linear Structure Formula :- InChI Key :YVKLUKXESFJRCE-UHFFFAOYSA-N
M.W : 192.23 Pubchem ID :821868
Synonyms :

Safety of [ 3133-78-6 ]

Signal Word:Warning Class:
Precautionary Statements:P305+P351+P338 UN#:
Hazard Statements:H302-H319 Packing Group:
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Application In Synthesis of [ 3133-78-6 ]

* 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 [ 3133-78-6 ]

[ 3133-78-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 3133-78-6 ]
  • [ 1121057-75-7 ]
  • [ 1251537-36-6 ]
YieldReaction ConditionsOperation in experiment
With benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; triethylamine; In N,N-dimethyl-formamide; at 20℃; Example 5: Tetrahydropyridine 5 was prepared in 2 steps starting with the deprotection of 1 usingMethod 3. The resulting HCl amine salt was dissolved in 7V,7V-dimethylformamide (0.2 M). 3- Methyl-l-benzothiophene-2-carboxylic acid (1.0 equiv) and PyBOP (1.0 equiv) were added followed by the dropwise addition of triethylamine (3.0 equiv). After stirring at room temperature for 30 min, the reaction was diluted with water and filtered. The isolated material was then purified using semi -preparatory liquid chromatography to isolate the fraction of desired boronic acid 5 that resulted from pinacol ester deprotection during the course of the acid coupling. [M-H]- = 300.1 m/z. Activity: B
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