Home Cart Sign in  
Chemical Structure| 59190-99-7 Chemical Structure| 59190-99-7

Structure of 59190-99-7

Chemical Structure| 59190-99-7

*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 [ 59190-99-7 ]

CAS No. :59190-99-7
Formula : C5H9NO4
M.W : 147.13
SMILES Code : C[C@H](NC(OC)=O)C(O)=O
MDL No. :MFCD12795173

Safety of [ 59190-99-7 ]

Application In Synthesis of [ 59190-99-7 ]

* 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 [ 59190-99-7 ]

[ 59190-99-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 59190-99-7 ]
  • [ 18650-39-0 ]
  • [ 1560645-02-4 ]
YieldReaction ConditionsOperation in experiment
90% With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In dichloromethane; at 0 - 20℃; for 3h; To a solution of compound 35-6 (1.0 g, 5.57 mmol), compound 7-3-2 (1.23 g, 8.38 mmol) and EDCI (2.142 g, 11.17 mmol) in DCM (40.0 mL) was added DIPEA (5.0 mL. 30.25 mmol) dropwise at 0 °C. At the end of addition, the mixture was stirred at rt for 3 hrs. After the reaction was completed, 40 mL of water was added, and the resulting mixture was extracted with CH2C12 (50 mL x 3). The combined organic layers were dried over Na2S04 and concentrated in vacuo. The residue was purified by a silica gel column chromatography (PE/EtOAc (v/v) = 2/1 ) to give the title compound as colorless liquid (1.36 g. 90percent). The compound was characterized by the following spectroscopic data: MS (ESI. pos. ion) m/z: 301.2 [M+H] +; NMR (400 MHz. CDCI3) delta (ppm): 5.44. 5.42 (br. br. 1 H). 5.04-5.02, 5.02-5.01 (m. m, 1 H), 4.56-4.49 (m. 1 H), 3.74-3.71 (m, 1 H), 3.70 (s, 3H), 3.64 (s, 3H), 3.14-3.07 (m. 2H). 2.14-2.06 (m, 2H). 1.35, 1.33 (s. s, 3H), 1.18-1.02 (m. 3H).
45.36% With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In dichloromethane; at 0 - 20℃; for 3h; 11659] To a solution of compound 35-6 (1.0 g, 5.57 mmol), compound 7-3-2 (1.23 g, 8.38 mmol) and EDCI (2.142 g, 11.17 mmol) in DCM (40.0 mE) was added DIPEA (5.0 mE,30.25 mmol) dropwise at 0° C. At the end of addition, the mixture was stirred at it for 3 hrs. Afier the reaction wascompleted, 40 mE of water was added, and the resulting mixture was extracted with CH2C12 (50 mLx3). The combined organic layers were dried over Na2SO4 and concentrated in vacuo. The residue was purified by a silica gel column chromatography (PE/EtOAc (v/v)=2/1) to give the title compound as colorless liquid (1.36 g, 90percent). The compound was characterized by the following spectroscopic data:11660] MS (ESI, pos. ion) mlz: 301.2 [M+H]11661] ?H NMR (400 MHz, CDC13) oe (ppm): 5.44,5.42 (br, br, 1H), 5.04-5.02, 5.02-5.01 (m, m, 1H), 4.56-4.49 (m, 1H), 3.74-3.71 (m, 1H), 3.70 (s, 3H), 3.64 (s, 3H), 3.14-3.07 (m, 2H), 2.14-2.06 (m, 2H), 1.35, 1.33 (s, s, 3H), 1.18-1.02 (m, 3H).
 

Historical Records