1112-24-9 Usage
Uses
Used in Cancer Therapy:
NSC17711 is used as an antineoplastic agent for its ability to inhibit the growth of cancer cells and induce apoptosis. It has shown potential in treating various types of cancer by modulating oncological signaling pathways and enhancing the efficacy of conventional chemotherapeutic drugs.
Used in Chemoprevention:
NSC17711 is used as a chemopreventive agent for its ability to reduce the formation of tumors in animal models. It demonstrates promising properties in preventing the development of cancer by inhibiting the initiation and progression of tumor growth.
Used in Pharmaceutical Industry:
NSC17711 is used as a potential therapeutic agent in the pharmaceutical industry for its diverse biological activities and potential applications in cancer treatment and prevention. Further research is needed to fully understand its mechanisms of action and to investigate its potential as a therapeutic agent in the treatment and prevention of cancer.
Check Digit Verification of cas no
The CAS Registry Mumber 1112-24-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,1 and 2 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1112-24:
(6*1)+(5*1)+(4*1)+(3*2)+(2*2)+(1*4)=29
29 % 10 = 9
So 1112-24-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H15NO3/c1-7(2)6(3-8,4-9)5-10/h8-10H,3-5H2,1-2H3
1112-24-9Relevant academic research and scientific papers
PROCESS FOR MAKING TERTIARY AMINOALCOHOL COMPOUNDS
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Page/Page column 13, (2012/04/17)
Provided is a process for making a tertiary aminoalcohol compound. The process comprises using an excess amount of a carbonyl compound in a condensation step between the carbonyl compound and a nitroalkane, and conducting a hydrogenation/alkylation step to produce the tertiary aminoalcohol. The process uses fewer steps than conventional processes.
ALKYLATION AND ACYLATION OF TRI(HYDROXYMETHYL)AMINOMETHANE
Boikov, Yu. A.,Bakhmenko, V. B.,V'yunov, K. A.,Ginak, A. I.
, p. 261 - 265 (2007/10/02)
The alkylation and acylation of tri(hydroxymethyl)aminomethane and tri(chloromethyl)aminomethane by methyl iodide and acetyl chloride are described.During cleavage of the quaternary ammonium base obtained by exhaustive Hofmann methylation, 1,3-dichloro-2-chloromethyl-1-propene was formed exclusively; it was also obtained from tri(chloromethyl)carbenium in a superacidic medium.The formation of the olefin was explained by competition between the two processes in the transformation of the reaction intermediate, taking place by SN1 and E1 mechanisms.
