Home Cart Sign in  
Chemical Structure| 195155-27-2 Chemical Structure| 195155-27-2

Structure of 195155-27-2

Chemical Structure| 195155-27-2

*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 [ 195155-27-2 ]

CAS No. :195155-27-2
Formula : C12H16N2O3S
M.W : 268.33
SMILES Code : O=CC1=CC=C(S(=O)(N2CCN(C)CC2)=O)C=C1

Safety of [ 195155-27-2 ]

Application In Synthesis of [ 195155-27-2 ]

* 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 [ 195155-27-2 ]

[ 195155-27-2 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 195155-27-2 ]
  • [ 57497-39-9 ]
  • [ 862499-61-4 ]
YieldReaction ConditionsOperation in experiment
Example 22 N-(tert-Butyl)-C-[4-(4-methyl-piperazine-1-sulfonyl)phenyl]nitrone (22) The title compound was prepared according to the procedure described in Example 20, starting from <strong>[57497-39-9]N-tert-butylhydroxylamine hydrochloride</strong> and 4-(4-methyl-piperazine-1-sulfonyl)benzaldehyde MS: m/z 340 (MH+).
  • 2
  • [ 109-01-3 ]
  • [ 85822-16-8 ]
  • [ 195155-27-2 ]
YieldReaction ConditionsOperation in experiment
With sodium hydrogencarbonate; In dichloromethane; water; for 1h; To a solution of <strong>[85822-16-8]4-formylbenzenesulfonyl chloride</strong> (1.0 g) in DCM (10 mL) was added NaHCO3 (sat'd aq, 10 mL) followed by 1-methyl-piperazine (0.6 mL). The reaction mixture was vigorously stirred for 1 h, the organic layer separated, and the aqueous layer extracted with DCM (2*20 mL). The combined organic extracts were washed with brine, dried over anhydrous Na2SO4, filtered and evaporated under reduced pressure to give 4-(4-methyl-piperazine-1-sulfonyl)-benzaldehyde (1.28 g) without further purification.
 

Historical Records

Technical Information

Categories