260970-57-8 Usage
Uses
Used in Pharmaceutical Synthesis:
4-(boc-aminomethyl)pyridine-2-carboxylic acid serves as a crucial building block in the development of pharmaceuticals, contributing to the creation of various medicinal compounds. Its unique structure allows for the synthesis of complex molecules that can target specific biological pathways, potentially leading to the discovery of new drugs with improved efficacy and selectivity.
Used in Agrochemical Production:
In the agrochemical industry, 4-(boc-aminomethyl)pyridine-2-carboxylic acid is utilized as a key intermediate for the synthesis of pesticides and other crop protection agents. Its ability to form complex molecules enables the development of innovative agrochemicals that can effectively protect crops from pests and diseases while minimizing environmental impact.
Used in Organic Chemistry Research:
As a versatile intermediate, 4-(boc-aminomethyl)pyridine-2-carboxylic acid is also employed in organic chemistry research for exploring novel chemical reactions and synthesis pathways. Its presence in the lab allows chemists to investigate the functionalization of the pyridine ring and carboxylic acid group, potentially uncovering new methods for the construction of complex organic molecules.
Used in the Synthesis of Complex Molecules:
4-(boc-aminomethyl)pyridine-2-carboxylic acid is used as a valuable tool for the synthesis of complex molecules due to its potential for further functionalization. The presence of the Boc-protected aminomethyl group and the carboxylic acid functionality provides a foundation for the attachment of various chemical moieties, facilitating the creation of intricate molecular structures with diverse applications across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 260970-57-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,0,9,7 and 0 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 260970-57:
(8*2)+(7*6)+(6*0)+(5*9)+(4*7)+(3*0)+(2*5)+(1*7)=148
148 % 10 = 8
So 260970-57-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H16N2O4/c1-12(2,3)18-11(17)14-7-8-4-5-13-9(6-8)10(15)16/h4-6H,7H2,1-3H3,(H,14,17)(H,15,16)
260970-57-8Relevant academic research and scientific papers
Huang, Xuefei,Borhan, Babak,Rickman, Barry H.,Nakanishi, Koji,Berova, Nina
, p. 216 - 224 (2000)
A nonempirical exciton chirality circular dichroic (CD) method for determining the absolute configurations of primary monoamines with amino group directly linked to the stereogenic center is described. Conventional exciton chirality CD method cannot be applied to these compounds since they lack the two sites for attaching the interacting chromophores. This was solved by covalently linking the monoamine to a trifunctional bidentate carrier moiety 1. Treatment of the carrier/monoamine conjugate with the porphyrin tweezer 4 consisting of two pentanediol-linked zinc porphyrins gives rise to 1:1 host-guest macrocyclic complexes that exhibit exciton- coupled CD spectra. The sign of the CD couplet can then be correlated with the absolute configuration of the monoamine as follows: a clockwise arrangement of the L, M, and S (large, medium, small) groups in the Newman projection of the monoamine with the amino group in the rear gives rise to a positive CD couplet, and vice versa; the assignments of L, M, S groups are based on conformational energies (A values). This method is applicable to cyclic and acyclic aliphatic amines, aromatic amines, amino esters, amides, and cyclic amino alcohols, and can be performed at the several microgram level.
