Home Cart Sign in  
Chemical Structure| 14618-77-0 Chemical Structure| 14618-77-0

Structure of 14618-77-0

Chemical Structure| 14618-77-0

*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 [ 14618-77-0 ]

CAS No. :14618-77-0
Formula : C5H7NO2
M.W : 113.11
SMILES Code : O=C(OC)C(C#N)C
MDL No. :MFCD00036017

Safety of [ 14618-77-0 ]

Application In Synthesis of [ 14618-77-0 ]

* 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 [ 14618-77-0 ]

[ 14618-77-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 36193-65-4 ]
  • [ 14618-77-0 ]
  • ethyl 2-cyano-2-(2-cyano-1H-indol-3-yl)propanoate [ No CAS ]
YieldReaction ConditionsOperation in experiment
58% With manganese(III) acetate dihydrate; acetic acid; for 24h;Reflux; General procedure: Cyanoindole 6 (40 mg, 0.256 mmol, 1 equiv.), Mn(OAc)3.2H2O (345 mg, 1.29 mmol, 5 equiv),and diethyl malonate (205 mg, 1.28 mmol, 5 equiv) were dissolved in aceticacid (10 mL) and heated to reflux for 2 h. After TLC indicated complete consumption of the starting indole, the reaction was poured into water (200 mL) and extracted with ethyl acetate (3 50 mL). The combined organic extracts were washed with water (3 100 mL), brine (1 100 mL), dried over sodium sulfate, filtered, and concentrated in vacuo to give a brown oil. The product was purified via flash chromatography (silica gel, hexanes:EtOAc 4:1)to afford 15 as a white solid (90%);20
 

Historical Records