Home Cart Sign in  
Chemical Structure| 88526-59-4 Chemical Structure| 88526-59-4

Structure of 88526-59-4

Chemical Structure| 88526-59-4

*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 [ 88526-59-4 ]

CAS No. :88526-59-4
Formula : C6H7N3S
M.W : 153.21
SMILES Code : NC(=S)C1=CC=NC(N)=C1
MDL No. :MFCD09932275

Safety of [ 88526-59-4 ]

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 [ 88526-59-4 ]

* 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 [ 88526-59-4 ]

[ 88526-59-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 42182-27-4 ]
  • [ 88526-59-4 ]
YieldReaction ConditionsOperation in experiment
81% With O,O-Diethyl hydrogen phosphorodithioate; In tetrahydrofuran; water; at 60℃; for 28h; [00616] (i) Production of 2-aminopyridine-4-carbothioamide[00617] A mixture of <strong>[42182-27-4]2-aminopyridine-4-carbonitrile</strong> (6.0 g, 50 mmol), O,O' -diethyl dithiophosphate (11 mL, 60 mmol), tetrahydrofuran (25 mL) and water (25 mL) was stirred at 600C for 4 hr. To the reaction mixture was added O,O'-diethyl dithiophosphate (2.8 mL, 15 mmol) and the mixture was stirred at 600C for 1 day. To the reaction mixture was added aqueous sodium bicarbonate solution, and the mixture was extracted with ethyl acetate. The combined organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate, and the insoluble material was filtered off. The filtrate was concentrated under reduced pressure, and the obtained residue was washed with diisopropyl ether to give the title compound (6.2 g, 81percent) as a yellow solid.[00618] 1H-NMR (DMSO-dbeta, 300 MHz) delta 6.12 (2H, s), 6.73 (IH, dd, J = 1.7, 5.3 Hz), 6.77 - 6.81 (IH, m), 7.92 (IH, dd, J = 0.6, 5.3 Hz), 9.53 (IH, br s), 9.95 (IH, br s).
47% With pyridine; diammonium sulfide; triethylamine; at 52℃; for 2h; General procedure: 40?48wt.percent aqueous ammonium sulfide (8.27ml, 48.5mmol) was added to a mixture of 57 (5.3g, 44.1mmol), triethylamine (6.14ml, 44.1mmol), and pyridine (28.8ml, 353mmol) and the resulting suspension was stirred at 52°C for 2h. The mixture was concentrated under reduced pressure and H2O was added to the residue. The mixture was chilled to 0°C and the resulting precipitate was removed by filtration to deliver 2-aminopyrimidine-4-carbothioamide (5.5g, 35.7mmol, 80percent yield) as a yellow solid.
 

Historical Records

Technical Information

Categories