106268-01-3 Usage
Usage
Synthesis of pharmaceuticals and other organic compounds
Chirality
Chiral compound with a specific three-dimensional arrangement of atoms
Application
Employed as a reagent in organic synthesis reactions
Bond Formation
Particularly used in the formation of carbon-carbon and carbon-nitrogen bonds
Structural and Reactivity
Unique structure and reactivity make it a valuable tool for chemists and researchers in organic chemistry
Safety Precaution
Should be handled with care due to potential for causing skin and respiratory irritation
Check Digit Verification of cas no
The CAS Registry Mumber 106268-01-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,2,6 and 8 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 106268-01:
(8*1)+(7*0)+(6*6)+(5*2)+(4*6)+(3*8)+(2*0)+(1*1)=103
103 % 10 = 3
So 106268-01-3 is a valid CAS Registry Number.
106268-01-3Relevant academic research and scientific papers
Anthracyclinones. 2. Isosaccharinic Acid as Chiral Template for the Synthesis of (+)-4-Demethoxy-9-deacetyl-9-(hydroxymethyl)daunomycinone and (-)-4-Deoxy-γ-rhodomycinone
Florent, J. C.,Ughetto-Monfrin, J.,Monneret, C.
, p. 1051 - 1056 (2007/10/02)
Chiral aldehyde derivatives 12, 19, and 22 were prepared in few steps from α-D-isosaccharino-1,4 lactone (1a).These derivative precursors of ring A of the title anthracyclinones were condensed with leucoquinizarin (28), the component of the BCD rings.Aldolization reactions afforded alkylanthraquinones 29, 33, and 34, respectively.After suitable transformations of 29 and ring closure, the protected anthracyclinone 27 was obtained.Acetal cleavage of 27 led to the (+)-4-demethoxy-9-deacetyl-9-(hydroxymethyl)daunomycinone (5).Similarly suitable transformations of 33 or 34 followed by ring closure gave the (-)-4-deoxy-γ-rhodomycinone (30).
