Home Cart Sign in  
Chemical Structure| 111398-44-8 Chemical Structure| 111398-44-8

Structure of 111398-44-8

Chemical Structure| 111398-44-8

*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 [ 111398-44-8 ]

CAS No. :111398-44-8
Formula : C7H13NO4
M.W : 175.18
SMILES Code : CC(C)C(NC(OC)=O)C(O)=O
MDL No. :MFCD11128988
InChI Key :CEFVHPDFGLDQKU-UHFFFAOYSA-N
Pubchem ID :13821101

Safety of [ 111398-44-8 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H312-H332
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P330-P363-P501

Application In Synthesis of [ 111398-44-8 ]

* 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 [ 111398-44-8 ]

[ 111398-44-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 18650-39-0 ]
  • [ 111398-44-8 ]
  • [ 1419390-17-2 ]
YieldReaction ConditionsOperation in experiment
80% With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In dichloromethane; at 0 - 20℃; for 3h; 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 the addition, the mixture was stirred at rt for 3.0 hrs. After the reaction was completed, 40 mL of water was added to the mixture, and the resulting mixture was extracted with CH2C12(35 mL x 3). The combined organic layers were washed with brine, dried over anhydrous Na2S04and concentrated in vacuo. The residue was purified by silica gel column chromatography (PE/EtOAc (v/v) = 2/1) to give the title compound as colorless liquid (1.337 g. 80percent). The compound was characterized by the following spectroscopic data:MS (ESI, pos.ion) mlz: 301.2 [M+H] ; and NMR (400 MHz. CDCU) (ppm): 5.32.5.29 (d, d.1H), 4.93-4.89 (m, 1H), 4.31-4.26 (m.1H), 3.70 (s. 3H), 3.67-3.64 (m.1H).3.63 (s.3H).3.11-3.02 (m. 1H).2.23-2.14 (m. 1H), 2.13-2.05 (m.2H), 1.20-1.02 (m, 4H), 0.97, 0.95 (m. m.3H).0.90, 0.89 (m, m, 3H).
 

Historical Records

Technical Information

Categories