Home Cart Sign in  
Chemical Structure| 50746-36-6 Chemical Structure| 50746-36-6

Structure of 50746-36-6

Chemical Structure| 50746-36-6

*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 [ 50746-36-6 ]

CAS No. :50746-36-6
Formula : C11H25NO2
M.W : 203.32
SMILES Code : CC(C)CN(C(OC)OC)CC(C)C

Safety of [ 50746-36-6 ]

Application In Synthesis of [ 50746-36-6 ]

* 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 [ 50746-36-6 ]

[ 50746-36-6 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 2591-76-6 ]
  • [ 77-78-1 ]
  • [ 50746-36-6 ]
  • 2
  • [ 2591-76-6 ]
  • 4-amino-3-hydro-7-(3,5-di-O-toluoyl-2-deoxy-beta-D-ribofuranosyl)-pyrrolo[2,3-d]pyrimidin-2-one [ No CAS ]
  • [ 50746-36-6 ]
  • 4-(N,N-diisobutyl-formamidine)-3-hydro-7-(3,5-di-O-toluoyl-2-deoxy-β-D-ribofuranosyl)-pyrrolo[2,3-d]pyrimidin-2-one [ No CAS ]
YieldReaction ConditionsOperation in experiment
In dichloromethane; at 20℃; 4-Amino-3-hydro-7-(3,5-di-O-toluoyl-2-deoxy-β-D-ribofuranosyl)-pyrrolo[2,3-d]pyrimidin-2-one (1.014 g, 2.02 mmol) is dissolved in CH2Cl2 (10 mL), Dimethoxymethyldiisobutylamine (2.5 mL of a 70% w/w solution in diisobutylformamide) is added dropwise. The solution is allowed to stir at room temperature overnight. The mixture is concentrated to small bulk (yellow oil) and resolved by chromatography using gradients of methylene chloride and methanol to afford a mixture of the two isomers. The mixture is then repurified to resolve the two isomers.
 

Historical Records