Home Cart Sign in  
Chemical Structure| 25468-51-3 Chemical Structure| 25468-51-3

Structure of 25468-51-3

Chemical Structure| 25468-51-3

*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 [ 25468-51-3 ]

CAS No. :25468-51-3
Formula : C13H11N3O3
M.W : 257.24
SMILES Code : O=C(C1=C(N2)N(N=C1)C3=C(C=CC=C3)C2=O)OCC
MDL No. :MFCD00173921
InChI Key :IIXIEYBXSSHPQB-UHFFFAOYSA-N
Pubchem ID :135407994

Safety of [ 25468-51-3 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Application In Synthesis of [ 25468-51-3 ]

* 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 [ 25468-51-3 ]

[ 25468-51-3 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 33906-30-8 ]
  • [ 94-05-3 ]
  • [ 25468-51-3 ]
YieldReaction ConditionsOperation in experiment
With sodium acetate; In water; N,N-dimethyl-formamide; EXAMPLE 1 A solution of 50 g. (0.27 mole) of <strong>[33906-30-8]2-hydrazinobenzoic acid hydrochloride</strong> [Pfanntiel et al., Ber. 75B, 1096-1107 (1942)], 45 g. (0.26 mole) of ethyl ethoxymethylenecyanoacetate and 26.4 g. (0.32 mole) of sodium acetate in 330 ml. of DMF was heated to 140 C., then cooled to ambient temperature, diluted with 130 ml. of water and chilled. The solid which separated was collected, washed with water, then with ethanol, then with diethyl ether and dried to give 62.6 g. of ethyl 4,5-dihydro-5-oxopyrazolo[1,5-a]quinazoline-3-carboxylate, m.p. 203-205 C.
  • 2
  • [ 33906-30-8 ]
  • [ 94-05-3 ]
  • [ 25468-51-3 ]
 

Historical Records

Technical Information

Categories