N-(4-Benzyloxy)benzyl Tri-O-(tert-butyldimethylsilyl) Ractopamine

• Catalog number
  B288035
• Price
  Please ask
• Size
  2,5 mg

• Chemical available in other sizes
  Please inquire size and price
• Stock availability
  Pending QC
• Cas number
  1797130-49-4
• Chemical s molecular weight
  840.41
• Chemical s main applications
  Ractopamine (R071400) derivative.
• Chemical s category
  Amines, Aromatics, Pharmaceuticals, Intermediates & Fine Chemicals
• Other name
  4-Hydroxy-α-[[[3-(4-hydroxyphenyl)-1-methylpropyl]-N-(4-benzyloxy)benzylamino]methyl]benzenemethanol Tri-(tert-butyldimethylsilyl) Ether
• Chemical s formula
  C50H77NO4Si3
• Physical properties
  Yellow Oil
• Melting temperature
  No Data Available
• Boiling temperature
  No Data Available
• Chemical s soluble in
  Methanol
• Stability conditions
  No Data Available
• Storage
  No Data Available
• Chemical s specifications

• Gene target
  4-Benzyloxy   benzyl   Tri-O   tert-butyldimethylsilyl   Ractopamine  
• Short name
  N-(4-Benzyloxy)benzyl Tri-O-(tert-butyldimethylsilyl) Ractopamine
• Alternative name
  N-(4-Benzyloxy)benzyl Tri-O-(telomerase reverse transcriptase-butyldimethylsilyl) Ractopamine
• Alternative to gene target
  telomerase reverse transcriptase, CMM9 and DKCA2 and DKCB4 and EST2 and hEST2 and hTRT and PFBMFT1 and TCS1 and TP2 and TRT, TERT and IDBG-10998 and ENSG00000164362 and 7015, telomeric RNA binding, nuclei, Tert and IDBG-165912 and ENSMUSG00000021611 and 21752, BT.60929 and IDBG-632169 and ENSBTAG00000012567 and 518884

MeSH Data

• Name
  Cloning, Molecular
• Concept
  Scope note: The insertion of recombinant DNA molecules from prokaryotic and/or eukaryotic sources into a replicating vehicle, such as a plasmid or virus vector, and the introduction of the resultant hybrid molecules into recipient cells without altering the viability of those cells.
• Tree numbers
  • E05.393.220
• Qualifiers
  drug effects, methods, radiation effects

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