Home Cart Sign in  
Chemical Structure| 21977-09-3 Chemical Structure| 21977-09-3

Structure of 21977-09-3

Chemical Structure| 21977-09-3

*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 [ 21977-09-3 ]

CAS No. :21977-09-3
Formula : C6H11NO2
M.W : 129.16
SMILES Code : O=CCN1CCOCC1
MDL No. :MFCD05663331
InChI Key :KKOPYUKQPCQGEM-UHFFFAOYSA-N
Pubchem ID :1519330

Safety of [ 21977-09-3 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 21977-09-3 ]

* 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 [ 21977-09-3 ]

[ 21977-09-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 3616-59-9 ]
  • [ 21977-09-3 ]
YieldReaction ConditionsOperation in experiment
Preparation of Intermediate 8Intermediate 7 Intermediate 8; [0209] A solution of Intermediate 7 (600 mg, 2.95 mmol) dissolved in concentrated aqueous HCI (4 mL) was stirred at 80 C for 2 h. The reaction mixture was cooled to RT, made alkaline (pH ~10) with saturated aqueous NaHC03 (20 mL) and the resulting solution was extracted with DCM (3 x 50 mL). The combined organic layers were washed with water (50 mL), brine (30 mL), dried over Na2S04, filtered and concentrated in vacuo to obtain crude Intermediate 8 (340 mg) as a colorless oil which was used without additional purification. TLC: 60% EtOAc in hexane: Rf: 0.30.
With hydrogenchloride; In water; for 2.0h;Reflux; Synthesis of compound 62.3. A solution of compound 62.2 (0.650g, 0.37mmol) in cone. HC1 (lOmL) was refluxed for 2h. After completion of the reaction, reaction mixture was allowed to cool at room temperature and dichloromethane (50mL) was added to it. Organic layer was separated out, washed with water (50mL) and brine (50mL) dried over sodium sulphate and used as such in the next step considering 100% yield of compound 62.3 (0.413 g, 100%).
With hydrogenchloride; In water; at 80℃; for 2.0h; A solution of Intermediate 7 (600 mg, 2.95 mmol) dissolved in concentrated aqueous HCl (4 mL) was stirred at 80 C. for 2 h. The reaction mixture was cooled to RT, made alkaline (pH10) with saturated aqueous NaHCO3 (20 mL) and the resulting solution was extracted with DCM (3×50 mL). The combined organic layers were washed with water (50 mL), brine (30 mL), dried over Na2SO4, filtered and concentrated in vacuo to obtain crude Intermediate 8 (340 mg) as a colorless oil which was used without additional purification. TLC: 60% EtOAcin hexane: Rf: 0.30.
 

Historical Records

Technical Information

Categories