Home Cart Sign in  
Chemical Structure| 594-43-4 Chemical Structure| 594-43-4

Structure of 594-43-4

Chemical Structure| 594-43-4

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

4.5 *For Research Use Only !

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

US Stock

Global Stock

In Stock
{[ item.pr_size ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

  • {[ item.pr_size ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of [ 594-43-4 ]

CAS No. :594-43-4
Formula : C3H8O2S
M.W : 108.16
SMILES Code : O=S(C)(CC)=O
MDL No. :MFCD00015543
InChI Key :YBJCDTIWNDBNTM-UHFFFAOYSA-N
Pubchem ID :79059

Safety of [ 594-43-4 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H317
Precautionary Statements:P261-P272-P280-P302+P352-P333+P313-P362+P364-P501

Application In Synthesis of [ 594-43-4 ]

* 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 [ 594-43-4 ]

[ 594-43-4 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 594-43-4 ]
  • [ 3144-09-0 ]
  • [ 1520-70-3 ]
  • 2
  • [ 327056-62-2 ]
  • [ 594-43-4 ]
  • C9H11FN2O2S [ No CAS ]
YieldReaction ConditionsOperation in experiment
40 g With hydrogenchloride; n-butyllithium; In tetrahydrofuran; hexane; water; at -78 - 20℃; for 0.5h; To a mixture of a 1.6 M solution of n-butyl lithium in hexane 100 mE and THF 160 mE was added dropwise a mixture of ethyl methyl sulfone 23 g and THF 20 mE at -78 C. The reaction mixtures were raised to 0 C. gradually, and then re-cooled to -78 C. To the reaction mixtures were added dropwise a mixture of 5-fluoro-2-cyano-pyridine 20 g and THF 20 mE at -78 C. The mixtures were raised to room temperature gradually, and then to the reaction mixtures was added 2N hydrochloric acid and the mixtures were stirred for 30 minutes. The resulting mixtures were extracted with ethyl acetate and the resulting organic layers were washed with saturated saline. The resulting mixtures were dried over anhydrous sodium sulfate, and concentrated under reduced pressure to give an intermediate compound 16 represented by the following formula 40 g. 1H-NMR (CDC13) ö: 8.57 (1H, d), 8.19 (1H, dd), 7.62-7.55 (1H, m), 4.97 (2H, s), 3.30 (2H, q), 1.47 (3H, t).
  • 3
  • [ 327056-62-2 ]
  • [ 594-43-4 ]
  • C9H10FNO3S [ No CAS ]
YieldReaction ConditionsOperation in experiment
40 g With hydrogenchloride; n-butyllithium; In tetrahydrofuran; hexane; at -78 - 20℃; for 0.5h; A mixture of 23 g of ethyl methyl sulfone and 20 mL of THF was added dropwise at -78 C. to a mixture of 100 mL of a 1.6 M n-butyllithium hexane solution and 160 mL of THF.The reaction mixture was gradually heated to 0 C. and then recooled to -78 C.To this reaction mixture, a mixture of 20 g of <strong>[327056-62-2]5-fluoro-2-cyanopyridine</strong> and 20 mL of THF was added dropwise at -78 C.After gradually raising the temperature to room temperature, 2N hydrochloric acid was added to the reaction mixture, and the mixture was stirred for 30 minutes.The resulting mixture was extracted with ethyl acetate, and the obtained organic layer was washed with saturated brine.The obtained organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure to obtain 40 g of intermediate 16 represented by the following formula.
40 g 10684] To a mixture of 1.6 M n-butyllithium-hexane solution 100 mL and THF 160 mL, a mixture of ethyl methyl sulfone 23 g and THF 20 mL was added dropwise at -78 C. Afier the mixture was gradually warmed to 0 C., the mixture was again cooled to -78 C. To the mixture, a mixture of <strong>[327056-62-2]5-fluoro-2-cyanopyridine</strong> 20 g and THF 20 mL was added dropwise at -78 C. After the mixture was gradually warmed to room temperature, to the reaction mixture was added 2N hydrochloric acid, and the reaction mixture was stirred for 30 minutes. The obtained mixture was extracted with ethyl acetate, and the resulting organic layer was washed with saturated brine. The resulting organic layer was dried over anhydrous sodium sulfate and then concentrated under reduced pressure to give the intermediate compound 12 shown below 40 g.10685] The intermediate compound 12: ‘H-NMR (CDC13) ö: 8.57 (1H, d), 8.19 (1H, dd), 7.62-7.55 (1H, m), 4.97 (2H, s), 3.30 (2H, q), 1.47 (3H, t).
 

Historical Records

Technical Information

Categories

Related Functional Groups of
[ 594-43-4 ]

Sulfones

Chemical Structure| 5687-92-3

A534359 [5687-92-3]

Thietane 1,1-dioxide

Similarity: 0.81