Home Cart Sign in  
Chemical Structure| 14227-95-3 Chemical Structure| 14227-95-3

Structure of 14227-95-3

Chemical Structure| 14227-95-3

*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 [ 14227-95-3 ]

CAS No. :14227-95-3
Formula : C7H10N2O
M.W : 138.17
SMILES Code : N#CCC(N1CCCC1)=O
MDL No. :MFCD00020838

Safety of [ 14227-95-3 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501

Application In Synthesis of [ 14227-95-3 ]

* 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 [ 14227-95-3 ]

[ 14227-95-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 114078-88-5 ]
  • [ 14227-95-3 ]
  • C10H12BrN3O [ No CAS ]
YieldReaction ConditionsOperation in experiment
75% With pyridine; In benzene; at 50℃; for 0.5h;Inert atmosphere; Sealed tube; In a 10 mL dry sealed reaction tube, sequentially add <strong>[114078-88-5]5-bromo-1,2,3-triazine</strong> 1a (15.9 mg, 0.10 mmol), 1- (cyanoacetyl) pyrrolidine 4b (24.9 mg, 0.18 mmol) And pyridine (31.6 mg, 0.40 mmol). After nitrogen substitution three times, solvent benzene (1.0 mL) was added, and the sealed reaction tube was placed at 50 C for 0.5 h. The reaction was monitored by TLC. After the reaction was completed, it was extracted with dichloromethane (3 * 10 mL). The organic phase was dried over anhydrous sodium sulfate and concentrated in vacuo. After column chromatography, the target product 12c (20.2 mg, 75%) was obtained.Test and characterize the product 12c, see Figures 2 to 4,The characterization results prove that 1-(cyanoacetyl)pyrrolidine 4b is the ketene imine structure formed by cyanomethyl group under alkaline conditions and reacts with <strong>[114078-88-5]5-bromo-1,2,3-triazine</strong> 1a, 1 -The carbonyl group of the amide in (cyanoacetyl)pyrrolidine 4b does not easily form an enol structure and reacts with <strong>[114078-88-5]5-bromo-1,2,3-triazine</strong> 1a.
 

Historical Records

Technical Information

Categories