5275-07-0 Usage
Uses
Used in Pharmaceutical Industry:
3-Pyridin-4-ylMethyl-1H-indole, 98+% C14H12N2, MW: 208.27 is used as a building block for the synthesis of various bioactive molecules in the pharmaceutical industry. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, 3-Pyridin-4-ylMethyl-1H-indole, 98+% C14H12N2, MW: 208.27 is utilized as a starting material for the synthesis of agrochemicals with potential applications in pest control and crop protection. Its versatility in chemical reactions enables the creation of novel compounds with improved efficacy and selectivity.
Used in Research Applications:
3-Pyridin-4-ylMethyl-1H-indole, 98+% C14H12N2, MW: 208.27 is also used in research applications for the investigation of its chemical properties and potential interactions with biological systems. Its high purity form makes it an ideal candidate for studying its reactivity and exploring its use in the development of new chemical entities.
Check Digit Verification of cas no
The CAS Registry Mumber 5275-07-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,7 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5275-07:
(6*5)+(5*2)+(4*7)+(3*5)+(2*0)+(1*7)=90
90 % 10 = 0
So 5275-07-0 is a valid CAS Registry Number.
5275-07-0Relevant academic research and scientific papers
NOVEL THIENOPYRROLE COMPOUNDS
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Page/Page column 41-42, (2011/07/06)
The invention provides a compound of Formula (I) pharmaceutically acceptable salts, pro-drugs, biologically active metabolites, stereoisomers and isomers thereof wherein the variable are defined herein. The compounds of the invention are useful for treati
A new efficient synthesis of 3-(4-pyridinyl)methylindoles
Zhou, Ping,Li, Yanfang,Meagher, Kristin L,Mewshaw, Richard G,Harrison, Boyd L
, p. 7333 - 7335 (2007/10/03)
A new efficient method for the preparation of 3-(4-pyridinyl)methylindoles has been developed. The new method involves coupling of indoles with 4-pyridinecarboxaldehyde to give 3-indolyl 4-pyridinyl methanols, which upon treatment with triethylsilane in the presence of trifluoroacetic acid afford 3-(4-pyridinyl)methylindoles in 64-76% overall yield.
Chemistry of indoles carrying basic functions. I. Transformation of hydroxyindolones into indoles
Moldvai, Istvan,Gacs-Baitz, Eszter,Szantay, Csaba
, p. 437 - 440 (2007/10/02)
3-Hydroxy-3--1H-indol-2-ones (1, 12) have been reduced with NaBH4/MeOH/t-BuOH.After acidic treatment, 2- and 3-substituted indoles (2, 11 and 13, 14, respectively) were obtained.The intermediates 3 and 4 of the rearrangenment were isolated and the effect of the pyridylmethyl groups on the rearrangenment has also been established.
