Home Cart Sign in  
Chemical Structure| 51278-28-5 Chemical Structure| 51278-28-5

Structure of 51278-28-5

Chemical Structure| 51278-28-5

*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 [ 51278-28-5 ]

CAS No. :51278-28-5
Formula : C5H11NaO3S2
M.W : 206.26
SMILES Code : O=S([O-])(SCCCCC)=O.[Na+]

Safety of [ 51278-28-5 ]

Application In Synthesis of [ 51278-28-5 ]

* 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 [ 51278-28-5 ]

[ 51278-28-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 16311-69-6 ]
  • [ 51278-28-5 ]
  • N-(3-(amyldisulfanyl)-5-hydroxypent-2-en-2-yl)-N-methylformamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
52% With sodium hydroxide; In water; at 20℃; for 1h;Inert atmosphere; General procedure: Under argon protection, to a 30 mL aqueous of quaternary ammonium salt 9 (14.3 g, 50.0 mmol) and sodium hydroxide (4.0 g, 100.0 mmol) was added S-substituted sodium thiosulfates 11a-11f (120.0 mmol). The reaction mixture was stirred for 1 h at room temperature. The resultant oily substance was extracted with ethyl acetate (450 mL) and the organic layer was dried over anhydrous Na2SO4 and concentrated under reduced pressure. Purification of the crude product by column chromatography with dichloromethane-methanol (100:1) as eluent gave a yellow oil.
 

Historical Records