Home Cart Sign in  
Chemical Structure| 112940-54-2 Chemical Structure| 112940-54-2

Structure of 112940-54-2

Chemical Structure| 112940-54-2

*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 [ 112940-54-2 ]

CAS No. :112940-54-2
Formula : C11H18ClN3O2S
M.W : 291.80
SMILES Code : CS(=O)(NC1=CC=C(N2CCNCC2)C=C1)=O.[H]Cl
MDL No. :MFCD22048034

Safety of [ 112940-54-2 ]

Application In Synthesis of [ 112940-54-2 ]

* 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 [ 112940-54-2 ]

[ 112940-54-2 ] Synthesis Path-Downstream   1~1

  • 1
  • N-{4-[4-(4-Aminopyrid-2-yl)piperazin-1-yl]phenyl}methanesulphonamide [ No CAS ]
  • [ 76439-45-7 ]
  • [ 112940-54-2 ]
  • [ 112940-68-8 ]
YieldReaction ConditionsOperation in experiment
With sodium hydrogencarbonate; In water; butan-1-ol; (i) N-{4-[4-(4-Nitro-1-oxidopyrid-3-yl)piperazin-1-yl]phenyl}methanesulphonamide A mixture of N-[(4-piperazin-1-yl)phenyl]methanesulphonamide hydrochloride (the product of Example 11, (iii) (0.59 g), <strong>[76439-45-7]3-chloro-4-nitropyridine-N-oxide</strong> (0.35 g) and sodium bicarbonate (0.50 g) in n-butanol (25 ml) was heated at 100 C. with stirring for 1.5 hours and then evaporated. The residue was stirred with water, filtered, and the solid was crystallized from methanol to give the title compound (0.55 g), m.p. 206-208 C. Found: C,48.77; H,4.91; N,17.52. C16 H19 N5 O5 S requires: C,48.84; H,4.87; N,17.80%.
 

Historical Records