Home Cart Sign in  
Chemical Structure| 37629-59-7 Chemical Structure| 37629-59-7

Structure of 37629-59-7

Chemical Structure| 37629-59-7

*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 [ 37629-59-7 ]

CAS No. :37629-59-7
Formula : C7H7NO2S
M.W : 169.20
SMILES Code : C/C([N+]([O-])=O)=C\C1=CC=CS1

Safety of [ 37629-59-7 ]

Application In Synthesis of [ 37629-59-7 ]

* 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 [ 37629-59-7 ]

[ 37629-59-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 37629-59-7 ]
  • [ 1194-22-5 ]
  • 2,6-dimethyl-5-(thiophen-2-yl)furo[2,3-d]pyrimidin-4-ol [ No CAS ]
YieldReaction ConditionsOperation in experiment
89% In water; at 90℃; for 2h;Green chemistry; General procedure: Typically, 2-aminopyrimidine-4,6-diol (1a, 0.5 mmol, 1.0 equiv)/<strong>[1194-22-5]2-methylpyrimidine-4,6-diol</strong> (1b, 0.5 mmol, 1.0 equiv), nitroolefins (2, 0.5 mmol, 1.0 equiv), as well as water (2.5 mL) were introduced into a 10 mL reaction vial. Then, the reaction vial was closed and stirred for given time at 90 C. Upon completion, the reaction mixture was cooled to room temperature and diluted with cold water (30 mL). The solid product was collected by filtration and was purified by recrystallization from hot 95% EtOH to afford the goal product 5-arylfuro[2,3-d]pyrimidin-4-ol (3) as off-white to yellow solid.
 

Historical Records