Select Region or Location
Americas
  • Argentina
  • Brazil
  • Canada
  • Mexico
  • United States
  • Other Americas
Europe
  • Austria
  • Belgium
  • Bulgaria
  • Croatia/Hrvatska
  • Cyprus
  • Czech Republic
  • Denmark
  • Estonia
  • Finland
  • France
  • Germany
  • Greece
  • Hungary
  • Ireland
  • Italy
  • Latvia
  • Liechtenstein
  • Lithuania
  • Luxembourg
  • Malta
  • Netherlands
  • Norway
  • Poland
  • Portugal
  • Romania
  • Slovak Republic
  • Slovenia
  • Spain
  • Sweden
  • Switzerland
  • Turkey
  • United Kingdom
  • Other Europe
Asia Pacific
  • Australia
  • China
  • India
  • Indonesia
  • Japan
  • Korea, Republic of
  • Malaysia
  • New Zealand
  • Philippines
  • Singapore
  • Thailand
  • Vietnam
  • Other Asia Pacific
Africa And Middle East
  • Egypt
  • Israel
  • Other Africa And Middle East
USD
Home Cart Sign in  
Chemical Structure| 5446-89-9 Chemical Structure| 5446-89-9

Structure of 5446-89-9

Chemical Structure| 5446-89-9

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

4.5 *For Research Use Only! Not for Human Use. We Do Not Sell to Patients.

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

DE Stock

US Stock

Asia Stock

Global Stock

In Stock
{[ item.pr_size ]}{[ size_append_text(item.pr_size, proInfo.prAm, 'list') ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

  • {[ item.pr_size ]}
    {[ size_append_text(item.pr_size, proInfo.prAm, 'list') ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of [ 5446-89-9 ]

CAS No. :5446-89-9
Formula : C6H6N4OS
M.W : 182.20
SMILES Code : OC1=C2N=CNC2=NC(SC)=N1
English Name :2-(Methylthio)-9H-purin-6-ol
MDL No. :MFCD22577761

Safety of [ 5446-89-9 ]

Application In Synthesis of [ 5446-89-9 ]

* 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 [ 5446-89-9 ]

[ 5446-89-9 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 5446-89-9 ]
  • [ 66191-23-9 ]
YieldReaction ConditionsOperation in experiment
33% With N,N-diethylaniline; trichlorophosphate for 1.5h; Reflux; 14 Example 14; 2-Methylthio-6-chloropurine2-Methylthioxanthine (65 g) was mixed with POCl3 (975 ml) and N,N-diethylaniline (97.5 ml). The mixture was refluxed with mechanical stirring for 90 min Excess POCl3 was removed in vacuo with rotary vacuum evaporator at 55-60° C. and the residue poured onto ice (0° C., 1.75 kg). The mixture was stirred for 10 min to complete hydrolysis of the POCl3 and extracted with ethyl acetate (4×2.5 l). The combined ethyl acetate extracts were washed with water and dried to give a dark solid. The crude solid was recrystallised with decolourisation by active carbon from ethanol and dried to constant weight over phosphorus pentoxide. Yield 23.6 g (33%). HPLC purity: 99%. TLC (chloroform/methanol, 9/1) without impurities.
  • 2
  • [ 5446-89-9 ]
  • [ 66191-23-9 ]
YieldReaction ConditionsOperation in experiment
23.6 g With N,N-diethylaniline; trichlorophosphate for 1.5h; Reflux; 9 Example 9 2-Methylthio-6-chloropurin Example 9 2-Methylthio-6-chloropurin 2-Methylthioxanthine (65 g) was mixed with POCl3 (975 ml) and N,N-diethylaniline (97.5 ml). Reaction mixture was then refluxed at mechanical stirring for 90 minutes. Excess POCl3 was removed by vacuum rotary evaporator at 55-60 °C and the residue was mixed with ice (0 °C, 1.75 kg) for 10 minutes (until total hydrolysis of POCI3 was achieved). The product was then extracted by ethyl acetate (4 x 2.5 1). The extracts were washed with water and evaporated to dryness, yielding a dark brown solid. The raw product was re-crystallized from ethanol with active carbon and dried to constant weight over phosphorus(V) oxide. Yield: 23.6 g (33%). HPLC purity: 99%. TLC (chloroform/methanol, 9/1) - no impurities.
 

Historical Records

Technical Information

Categories