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[ CAS No. 7795-95-1 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
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Chemical Structure| 7795-95-1
Chemical Structure| 7795-95-1
Structure of 7795-95-1 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 7795-95-1 ]

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Product Details of [ 7795-95-1 ]

CAS No. :7795-95-1 MDL No. :MFCD00014729
Formula : C8H17ClO2S Boiling Point : No data available
Linear Structure Formula :- InChI Key :WIVNTNLDTMNDNO-UHFFFAOYSA-N
M.W : 212.74 Pubchem ID :82261
Synonyms :

Safety of [ 7795-95-1 ]

Signal Word:Danger Class:8
Precautionary Statements:P280-P305+P351+P338-P310 UN#:3265
Hazard Statements:H314 Packing Group:Ⅱ
GHS Pictogram:

Application In Synthesis of [ 7795-95-1 ]

* 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 [ 7795-95-1 ]

[ 7795-95-1 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 7795-95-1 ]
  • [ 120-35-4 ]
  • 4-Methoxy-3-(octane-1-sulfonylamino)-N-phenyl-benzamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
Example 178 4-Methoxy-3-(octane-1-sulfonylamino)-N-phenyl-benzamide The title compound has been made using the procedure of Example 127, but using 3-amino-4-methoxy-N-phenyl benzamide and 1-octanesulfonyl chloride as a starting material, which are commercially available from Aldrich and Lancaster; m.p. 154-155 C.
  • 2
  • [ 6174-86-3 ]
  • [ 7795-95-1 ]
  • 3-chloro-4-methyl-2-oxo-2H-chromen-7-yl octane-1-sulfonate [ No CAS ]
YieldReaction ConditionsOperation in experiment
73% With triethylamine; In tetrahydrofuran; at 20℃; for 4h; General procedure: Coumarin sulfonates 1-38 were synthesized by reactingdifferent hydroxylated coumarin derivatives (1 mmol) withcommercially available sulfonyl chlorides derivatives (1.2 mmol) inTHF (15 mL) and triethyl amine (1 mmol) was used as base. Reactionmixture was stirred for 4 h at room temperature to afford avariety of coumarin sulfonate esters 1e38. TLC monitoring wasused to determine the progress of the reaction. After the completionof reaction, THF was evaporated under reduced pressure andthe solid product obtained was washed with distilled water anddried under vacuum. The products were recrystallized in methanoland gave good yields. All the synthetic compounds 1-38 werecharacterized by different spectroscopic techniques such as EI-MS,HREI-MS, 1H-NMR, and 13C-NMR.
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