Cas 856781-76-5,(1S,2S)-N1-benzyl-N2-(tert-butoxycarbonyl)-2-amino-1-(4-fluorophenyl)-N1-hydroxy-aminobutane

856781-76-5

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Basic information

Product Name: (1S,2S)-N¹-benzyl-N²-(tert-butoxycarbonyl)-2-amino-1-(4-fluorophenyl)-N¹-hydroxy-aminobutane
Synonyms:
CAS NO:856781-76-5
Molecular Formula:
Molecular Weight: 388.482
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (1S,2S)-N¹-benzyl-N²-(tert-butoxycarbonyl)-2-amino-1-(4-fluorophenyl)-N¹-hydroxy-aminobutane(CAS DataBase Reference)
NIST Chemistry Reference: (1S,2S)-N¹-benzyl-N²-(tert-butoxycarbonyl)-2-amino-1-(4-fluorophenyl)-N¹-hydroxy-aminobutane(856781-76-5)
EPA Substance Registry System: (1S,2S)-N¹-benzyl-N²-(tert-butoxycarbonyl)-2-amino-1-(4-fluorophenyl)-N¹-hydroxy-aminobutane(856781-76-5)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 856781-76-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 856781-76-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,6,7,8 and 1 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 856781-76:
(8*8)+(7*5)+(6*6)+(5*7)+(4*8)+(3*1)+(2*7)+(1*6)=225
225 % 10 = 5
So 856781-76-5 is a valid CAS Registry Number.

856781-76-5Upstream product

856781-76-5Downstream Products

856781-76-5Relevant academic research and scientific papers

Enantiomerically pure [1,2-diamino-1-(4-fluorophenyl)butane]platinum(II) complexes: Synthesis and antitumor activity against MCF-7 and MDA-MB 231 breast cancer and LnCaP/FGC prostate cancer cell lines

Dullin, Anja,Dufrasne, Francois,Gelbcke, Michael,Gust, Ronald

, p. 654 - 667 (2004)

Enantiomerically pure 1,2-diamino-1-(4-fluorophenyl)butanes were synthesized by stereoselective procedures. The enantiomeric purity was determined by 1H NMR spectroscopy after derivatization with (1R)-myrtenal. For the coordination to platinum,

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