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Chemical Structure| 774597-13-6 Chemical Structure| 774597-13-6

Structure of 774597-13-6

Chemical Structure| 774597-13-6

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Product Details of [ 774597-13-6 ]

CAS No. :774597-13-6
Formula : C10H22BNO2Si
M.W : 227.18
SMILES Code : C[Si](/C=C/CB1OCCNCCO1)(C)C
MDL No. :N/A
InChI Key :OIZDHLXQPPZNRT-ONNFQVAWSA-N
Pubchem ID :11276221

Safety of [ 774597-13-6 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501

Application In Synthesis of [ 774597-13-6 ]

* 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 [ 774597-13-6 ]

[ 774597-13-6 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 121584-52-9 ]
  • [ 774597-13-6 ]
  • C68H123N11O14Si [ No CAS ]
  • [ 514854-24-1 ]
YieldReaction ConditionsOperation in experiment
With acetic acid; In dichloromethane; water; at 20℃; 7.375 g (32.46 mmol, 2 equiv.) of diethanolamine complex of formula V, 20 g (16.23 mmol, 1 equiv. ) <strong>[121584-52-9]acetyl-cyclosporin A aldehyde</strong> and 80 ml dichloromethane were charged in the reaction vessel at RT. 40 ml water and 2.79 ml (48.69 mmol, 3 equiv. ) acetic acid were added under stirring. After 10 min. stirring, a clear biphasic mixture was obtained. The reaction was monitored by HPLC.
With acetic acid; at 20℃; After ca 6 hours reaction at RT, 60 ml formic acid were added, maintaining the temperature below 30 C. The clear light yellow solution was stirred overnight at RT. 18 ml dichloromethane and 300 ml MTBE were added followed by 180 ml of a 10% NaClaq solution. The aqueous phase was separated and discarded. The organic phase was washed with 180 ml water, 300 ml 2M aqueous NAOH and 90 ml water. The organic phase was concentrated at RT under reduced pressure. The crystallization started and the suspension was diluted by addition of 300 ml MTBE and concentrated to ca 330 ml. After stirring 3 hours at RT and 1 hour at 0-2 C, the white suspension was filtered. The crystals were washed with 50 ML MTBE and dried at 50 C under reduced pressure to give 27. 4 G of (E)-acetyl-ISA247 as a white powder in >98% double bond isomeric purity by NMR.
  • 2
  • [ 121584-52-9 ]
  • [ 774597-13-6 ]
  • [ 515814-02-5 ]
YieldReaction ConditionsOperation in experiment
With boron trifluoride diethyl etherate; In dichloromethane; at -40 - 20℃; for 1.83333h; 1 g (0.82 mmol, 1 equiv.) acetyl-cyclsoporine A aldehyde were dissolved in 10 ml dichloromethane followed by 369 mg (1.62 mmol, 2 equiv. ) diethanolamine complex of formula V obtained by the method described in Example 3, i). The turbid solution was cooled TO-40 C. 180 UL (369 mmol, 2 equiv. ) boron trifluoride etherate were added keeping the temperature BELOW-40 C. After 1 hour AT-40 C, the cooling bath was removed and the reaction mixture was warmed up to RT. After 50 min. reaction at RT, 15 ml of a 5% aqueous NAHCO3 solution were added. The aqueous phase was separated and re-extracted with 15 ml dichloromethane. The combined organic phases were dried over MGS04, filtered and concentrated under reduced pressure at 40 C to give 0.99 g of (E)-ACETYL- ISA247 in >95% double bond isomeric purity (NMR) as a white foam.
 

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