147410-09-1 Usage
Chemical Class
Amino sugars
Structure
Bent structure with a benzylidene group attached to the ribose ring
Utility
Essential building block in the synthesis of various pharmaceuticals and bioactive compounds
Application
Key intermediate in the synthesis of nucleosides and nucleotides
Function
Crucial component in the construction of bioactive molecules and drug candidates
Importance
Vital compound in medicinal chemistry and drug discovery
Check Digit Verification of cas no
The CAS Registry Mumber 147410-09-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,4,1 and 0 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 147410-09:
(8*1)+(7*4)+(6*7)+(5*4)+(4*1)+(3*0)+(2*0)+(1*9)=111
111 % 10 = 1
So 147410-09-1 is a valid CAS Registry Number.
147410-09-1Relevant articles and documents
Stereoselective synthesis of 4,5-dihydroxy-D-erythro- and 4,5-dihydroxy-D-threo-L-norvaline from D-ribonolactone
Ariza,Diaz,Font,Ortuno
, p. 1315 - 1326 (2007/10/02)
Nitrogen functions have been introduced stereoselectively at the C-2 position in D-ribonolactone derivatives in order to prepared the title unnatural amino acids. The synthetic strategies lie in the inversion of configuration in S(N)2-type substitution re
An efficient and concise entry to (-)-4,5-dihydroxy-d-threo-l norvaline. Formal synthesis of clavalanine
Ariza, Jesus,Font, Josep,Ortuno, Rosa M.
, p. 1979 - 1982 (2007/10/02)
The title amino acid (2) has been synthesized for the first time in a seven-step sequence from D-ribonolactone, in 20% overall yield. Since the N-carbamoyl derivative of (2) in its y-lactone form has been used to prepare clavalanine, a formal total synthe
