Home Cart Sign in  
Chemical Structure| 212578-38-6 Chemical Structure| 212578-38-6

Structure of 212578-38-6

Chemical Structure| 212578-38-6

*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 [ 212578-38-6 ]

CAS No. :212578-38-6
Formula : C10H11NO3
M.W : 193.20
SMILES Code : O=C(C1CN(C)C2=CC=CC=C2O1)O
MDL No. :MFCD11506351

Safety of [ 212578-38-6 ]

Application In Synthesis of [ 212578-38-6 ]

* 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 [ 212578-38-6 ]

[ 212578-38-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 62058-03-1 ]
  • [ 212578-38-6 ]
  • C20H26N2O3 [ No CAS ]
YieldReaction ConditionsOperation in experiment
Example B .5 Preparation of compound 6; iV-(ethylcarbonimidoyl)-iV,iV-dimethyl-l,3-propanediamine, monohydrochloride [25952-53-8] (0.0022 mol) and 1 -hydroxy- lH-benzotriazole (0.0022 mol) were added to a solution of intermediate 6 [212578-38-6] (0.002 mol) in DMF (25 ml) and the mixture was stirred and warmed (40°C). Then a solution of 4-amino- (lalpha,3alpha,4alpha,5beta,7alpha) tricyclo[3.3.1.13'7]decan-l-ol [62058-03-1] (0.0024 mol) in hot DMF was added and the reaction mixture was stirred overnight at room temperature. The mixture was poured out into ice-water and was extracted with EtOAc. The obtained extract was washed with water and with brine and then dried and concentrated, yielding 0.040 g of compound 6. Example B .6
 

Historical Records

Technical Information

Categories