Home Cart Sign in  
Chemical Structure| 143426-47-5 Chemical Structure| 143426-47-5

Structure of 143426-47-5

Chemical Structure| 143426-47-5

*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 [ 143426-47-5 ]

CAS No. :143426-47-5
Formula : C12H12N2O2
M.W : 216.24
SMILES Code : O=C(OCC)C1=CC=C(N2N=CC=C2)C=C1
MDL No. :MFCD05994003

Safety of [ 143426-47-5 ]

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

Application In Synthesis of [ 143426-47-5 ]

* 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.

  • Upstream synthesis route of [ 143426-47-5 ]

[ 143426-47-5 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 143426-47-5 ]
  • [ 143426-49-7 ]
YieldReaction ConditionsOperation in experiment
49.6 g With sodium tetrahydroborate; calcium chloride In tetrahydrofuran for 64 h; Cooling with ice; Reflux G) . [4- (lH-pyrazol-l-yl) phenyl ] methanol To a solution of ethyl 4- ( lH-pyrazol-l-yl ) benzoate (73.7 g) in THF (500 mL) were added sodium borohydride (19.5 g) and calcium chloride (56.8 g) under ice-cooling, and the mixture was stirred at room temperature for 16 hr, and then heated with reflux for 2 days. The reaction mixture was diluted with IN hydrochloric acid, and the mixture was extracted with ethyl acetate (x 4). The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was washed with tert-butyl methyl ether to give the title compound (49.6 g) . 1HNMR (400 MHz, CDC13) δ 2.79 (1H, brs) , 4.68 (2H, s) , 6.45 (1H, t, J = 2.0 Hz), 7.38 (2H, d, J = 7.6 Hz), 7.61 (2H, d, J = 8.4 Hz) , 7.70 (1H, s), 7.89 (1H, d, J = 1.6 Hz).
References: [1] European Journal of Medicinal Chemistry, 1992, vol. 27, # 3, p. 219 - 228.
[2] Patent: WO2015/163485, 2015, A1, . Location in patent: Paragraph 0387.
 

Historical Records

Technical Information

Categories