Home Cart Sign in  
Chemical Structure| 1427319-44-5 Chemical Structure| 1427319-44-5

Structure of 1427319-44-5

Chemical Structure| 1427319-44-5

*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 [ 1427319-44-5 ]

CAS No. :1427319-44-5
Formula : C6H9NO
M.W : 111.14
SMILES Code : O=C1C(C2)CC2CN1
MDL No. :MFCD27991731

Safety of [ 1427319-44-5 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P280-P305+P351+P338

Application In Synthesis of [ 1427319-44-5 ]

* 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 [ 1427319-44-5 ]

[ 1427319-44-5 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 744212-68-8 ]
  • [ 1427319-44-5 ]
  • 2
  • [ 1352925-73-5 ]
  • [ 1427319-44-5 ]
YieldReaction ConditionsOperation in experiment
94% With ammonia; lithium; In tetrahydrofuran; tert-butyl alcohol; at -78℃; Compound 7 (1.5 g, 7.45 mmol) was dissolved in anhydrous THF/tBuOH, 10:1(10 mL) and the mixture was added to a stirring liquid ammonia at -78 C. Metallic Li pellets were added slowly to the stirring solution until a constant blue/black colour was observed. The reaction was then quenched by the addition of solid ammonium chloride. After removal of the NH3, EtOAc (30 mL) and H20 (8 ml) were added. The organic layer was separated and the aqueous layer was extracted with EtOAc (3 x 15 mL). The organic layers were combined, dried over Mg504 and concentrated in vacuo. The crude oil was filtered through a short silica column (cyclohexane/EtOAc, 1:1) to give Compound 8(800mg, 94% yield) as a yellow oil. (Rf= 0.1, cyclohexane/EtOAc, 50:50). H (500 IVIFIz; CD3OD) 7.46-7.13 (1H, m, NH) 3.43 (2H, d, J= 2.0, NCH2), 2.8 1-2.71 (1H, m, NCH2CI]), 2.60 (1H, q, J=5.6 Hz, C=OCH), 2.48-2.37 (2H, m, C=OCH(CHH)2, 1.70-1.62 (2H, m, C=OCH(CHJ])2). C (126 IVIFIz; CD3OD) 181.5, 46.3, 42.0, 34.3, 31.4; m/z (EI+) 111.0684 (M+W C6H9NO requires 111.0684).
 

Historical Records

Technical Information

Categories