869901-24-6 Usage
Uses
Used in Organic Synthesis:
4-[6-(TRIBUTYLSTANNYL)-2-PYRIDINYL]MORPHOLINE is used as a reagent for the synthesis of biaryl compounds. The tributylstannyl group acts as a functional group that can participate in various reactions, facilitating the formation of complex organic molecules.
Used in Pharmaceutical Development:
4-[6-(TRIBUTYLSTANNYL)-2-PYRIDINYL]MORPHOLINE is investigated for its potential use in the development of pharmaceuticals. Its unique chemical properties make it a candidate for creating new drugs with specific therapeutic effects.
Used in Agrochemical Development:
Similarly, 4-[6-(TRIBUTYLSTANNYL)-2-PYRIDINYL]MORPHOLINE is also being explored for its application in the development of agrochemicals. The distinctive characteristics of 4-[6-(TRIBUTYLSTANNYL)-2-PYRIDINYL]MORPHOLINE could contribute to the creation of novel agrochemicals with improved performance and selectivity in agricultural applications.
Check Digit Verification of cas no
The CAS Registry Mumber 869901-24-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,9,9,0 and 1 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 869901-24:
(8*8)+(7*6)+(6*9)+(5*9)+(4*0)+(3*1)+(2*2)+(1*4)=216
216 % 10 = 6
So 869901-24-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H11N2O.3C4H9.Sn/c1-2-4-10-9(3-1)11-5-7-12-8-6-11;3*1-3-4-2;/h1-3H,5-8H2;3*1,3-4H2,2H3;/rC21H38N2OSn/c1-4-7-17-25(18-8-5-2,19-9-6-3)21-12-10-11-20(22-21)23-13-15-24-16-14-23/h10-12H,4-9,13-19H2,1-3H3
869901-24-6Relevant academic research and scientific papers
ANTIBACTERIAL COMPOSITIONS
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Page/Page column 65-66, (2008/06/13)
Compounds of formula (I) have antibacterial activity: wherein: m is 0 or 1 ; Q is hydrogen or cyclopropyl; AIk is an optionally substituted, divalent C1-C6 alkylene, alkenylene or alkynylene radical which may contain an ether (-O-), thioether (-S-) or amino (-NR)- link, wherein R is hydrogen, -CN or C1-C3 alkyl; X is -C(=O)NR6-, -S(O)NR6-, -C(=O)O- or -S(=O)O- wherein R6 is hydrogen, optionally substituted C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl, -Cyc, or -( C1-C3 alkyl)-Cyc wherein Cyc is optionally substituted monocyclic carbocyclic or heterocyclic having 3-7 ring atoms; Z is N or CH, or CF; R2 and R3 are as defined in the description.
