Home Cart Sign in  
Chemical Structure| 793658-98-7 Chemical Structure| 793658-98-7

Structure of 793658-98-7

Chemical Structure| 793658-98-7

*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 [ 793658-98-7 ]

CAS No. :793658-98-7
Formula : C8H15NO3
M.W : 173.21
SMILES Code : O=C(C1(CN)CCOCC1)OC
MDL No. :MFCD07784123

Safety of [ 793658-98-7 ]

Application In Synthesis of [ 793658-98-7 ]

* 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 [ 793658-98-7 ]

[ 793658-98-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 793658-98-7 ]
  • [ 1455091-10-7 ]
  • [ 1455091-29-8 ]
YieldReaction ConditionsOperation in experiment
48 mg In methanol; at 150℃; for 10.8333h;Microwave irradiation; After a mixture of 4-hydroxy-7-phenoxy-isoquinoline-3-carboxylic acid methyl ester (121 mg), 4-aminomethyl-tetrahydro-pyran-4-carboxylic acid methyl ester (177 mg; commercially available) in MeOH (3 mL) was microwaved at 150 C for 650 min; cooled, concentrated, the residue was partitioned between EtOAc and diluted HCl solution, EtOAc phase was washed with water and diluted NaCl solution, dried over anhydrous sodium sulfate, filtered, concentrated and column purified to give product (48 mg). LC MS ESI+: 437 (M+l)+.
 

Historical Records