Home Cart Sign in  
Chemical Structure| 17242-85-2 Chemical Structure| 17242-85-2

Structure of 17242-85-2

Chemical Structure| 17242-85-2

*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 [ 17242-85-2 ]

CAS No. :17242-85-2
Formula : C10H19FN2O2Si2
M.W : 274.44
SMILES Code : FC1=CN=C(N=C1O[Si](C)(C)C)O[Si](C)(C)C
MDL No. :MFCD00042441
InChI Key :MPVQFVDWJDULDL-UHFFFAOYSA-N
Pubchem ID :140203

Safety of [ 17242-85-2 ]

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

Application In Synthesis of [ 17242-85-2 ]

* 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 [ 17242-85-2 ]

[ 17242-85-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 58042-39-0 ]
  • [ 17242-85-2 ]
  • [ 91286-55-4 ]
YieldReaction ConditionsOperation in experiment
In dichloromethane; water; SYNTHESIS EXAMPLE 1 1-Amino-5-fluorouracil 5-Fluorouracil was silylated as usual with hexamethyldisilazane, and then 8.8 g (32 mmole) of 2,4-ditrimethylsilyloxy-5-fluoropyrimidine thus obtained, distilled and purified was dissolved in dichloromethane (48 ml). To the solution was added 7.5 g (35 mmole) of <strong>[58042-39-0]mesitylenesulfonylhydroxylamine</strong> (<strong>[58042-39-0]MSH</strong>) under ice-cooling, and the mixture was reacted with stirring at room temperature for 4 hours. After reaction, the reaction solution was concentrated under reduced pressure. Distilled water (200 ml) was added to the residue, and oily impurities were extracted with chloroform (50 ml) from the mixture. The aqueous phase was neutralized with a weakly basic resin and then concentrated to dryness under reduced pressure. The crude crystal thus obtained was purified by sublimation under the conditions of 150 C. and 5 mmHg to give 2.9 g (yield, 62%) of 1-amino-5-fluorouracil. The product was further recrystallized from 50% ethanol to give colorless needle crystals. M.P. 196-199 C. (lit. 205-207 C.) Elementary analysis for C4 H4 N3 O2 F:
 

Historical Records

Technical Information

Categories