Home Cart Sign in  
Chemical Structure| 955127-80-7 Chemical Structure| 955127-80-7

Structure of 955127-80-7

Chemical Structure| 955127-80-7

*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 [ 955127-80-7 ]

CAS No. :955127-80-7
Formula : C9H8N2O
M.W : 160.17
SMILES Code : O=CC1=CC2=C(NN=C2C)C=C1
MDL No. :MFCD16987568
InChI Key :FGBHCSVATHXMLX-UHFFFAOYSA-N
Pubchem ID :45121478

Safety of [ 955127-80-7 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319
Precautionary Statements:P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313

Application In Synthesis of [ 955127-80-7 ]

* 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 [ 955127-80-7 ]

[ 955127-80-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 955127-80-7 ]
  • [ 34956-31-5 ]
  • [ 1086626-76-7 ]
YieldReaction ConditionsOperation in experiment
32% Step l (E)-l-(4-amino-2-methyIphenyI)-3-(3-methyI-lH-iϖdazol-5-yl)prop-2-en-l-one[00217] To a solution of KOH (1.5 g, 26 mmol) in 20 mL ethanol were added 3 -methyl- IH- indazole-5-carbaldehyde (see Note 1 for synthesis) (0.850 g, 5.3 mmol) and commercially available <strong>[34956-31-5]N-(4-acetyl-3-methylphenyl)acetamide</strong> (1.0 g, 5.3 mmol). The reaction mixture was heated to 80 C for 24 hours and then cooled down to room temperature. After acidification with IN HCl, the mixture was brought to pH 8 with saturated aqueous NaHCO3 and extracted twice with ethyl acetate (2 x 100 mL). The combined organic phases were washed with brine, dried over Na2SO4, filtered, and concentrated in vacuo. The product was purified by SiO2 flash chromatography (60:40 to 50:50 hexanes/ethyl acetate) to afford (E)-I -(4-amino-2- methylphenyl)-3-(3-methyl-lH-indazol-5-yl)prop-2-en-l-one (0.500 g, 32%). 1H NMR (400 MHz, d6-DMSO): δ 12.8 (s, IH), 8.12 (s, IH), 7.81 (dd, IH), 7.78 (d, IH), 7.61 (d, 2H), 7.48 (d, IH), 6.45 (m, 2H), 5.88 ( br s, IH), 3.06 (s, 3H), 2.42 (s, 3H); MS (EI) for C18HnN3O: 292.3 (MH+).
 

Historical Records

Technical Information

Categories