110544-97-3 Usage
General Description
BOC-D-2-AAD-OH, also known as Boc-D-2-Aminoadipic Acid, is a chemical compound primarily used in the field of peptide synthesis. It has the molecular formula of C11H19NO6 and the weight of 259.27. BOC-D-2-AAD-OH belongs to the "protected amino acids" category, where the BOC (tert-butoxycarbonyl) group serves as a protecting agent for the amino group. This allows for the amino acid to undergo various chemical reactions without the amino group being affected. BOC-D-2-AAD-OH is often utilized in pharmaceutical research, particularly in the creation of peptide-based drugs. Its handling requires caution as it can potentially cause eye and skin irritation, as well as respiratory problems if inhaled. Always ensure safe handling and storage of the chemical.
Check Digit Verification of cas no
The CAS Registry Mumber 110544-97-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,5,4 and 4 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 110544-97:
(8*1)+(7*1)+(6*0)+(5*5)+(4*4)+(3*4)+(2*9)+(1*7)=93
93 % 10 = 3
So 110544-97-3 is a valid CAS Registry Number.
110544-97-3Relevant articles and documents
Controlling the position of functional groups at the liquid/solid interface: Impact of molecular symmetry and chirality
De Cat, Inge,Gobbo, Cristian,Van Averbeke, Bernard,Lazzaroni, Roberto,De Feyter, Steven,Van Esch, Jan
supporting information; experimental part, p. 20942 - 20950 (2012/02/13)
With the aim of controlling the position of functional groups in a substrate-supported monolayer, a new family of functionalized linear alkyl chains was designed and synthesized, aided by molecular mechanics and dynamics simulations of its two-dimensional self-assembly on graphite. The self-assembly of these amino functionalized diamides at the liquid/solid interface was investigated with scanning tunneling microscopy. Intermolecular hydrogen-bonding interactions involving amides, combined with the effect of molecular symmetry and chirality, were found to guide the self-assembly. Control of the relative position and orientation of the amine groups was achieved, in the case of enantiopure compounds. Interestingly, racemates led to both racemic conglomerate and solid solution formation, with a concomitant loss of positional and orientational control of the amino groups as a result.
