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(isoquinolin-4-yl)methanol is a chemical compound belonging to the class of isoquinoline alkaloids, derived from isoquinoline, a nitrogen-containing heterocyclic compound. It exhibits diverse biological activities, such as antifungal, antibacterial, and antiviral properties, and holds potential in the pharmaceutical industry for various applications.

73048-60-9

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73048-60-9 Usage

Uses

Used in Pharmaceutical Industry:
(isoquinolin-4-yl)methanol is used as a compound with diverse biological activities for its antifungal, antibacterial, and antiviral properties, making it a promising candidate for the development of new drugs and therapies.
Used in Organic Synthesis:
(isoquinolin-4-yl)methanol is used as a precursor in organic synthesis, contributing to the creation of new chemical compounds and materials.
Used in Drug Development:
(isoquinolin-4-yl)methanol is used as a building block in the development of new drug candidates, leveraging its potential biological activities and chemical properties to design innovative pharmaceuticals.

Check Digit Verification of cas no

The CAS Registry Mumber 73048-60-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,0,4 and 8 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 73048-60:
(7*7)+(6*3)+(5*0)+(4*4)+(3*8)+(2*6)+(1*0)=119
119 % 10 = 9
So 73048-60-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H9NO/c12-7-9-6-11-5-8-3-1-2-4-10(8)9/h1-6,12H,7H2

73048-60-9Relevant academic research and scientific papers

INHIBITORS OF MLH1 AND/OR PMS2 FOR CANCER TREATMENT

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Paragraph 00519-00520, (2021/12/28)

The present invention relates to compounds of Formula (I) that target the MLH1 and/or PMS2 proteins that are components of the DNA Mismatch Repair (MMR) process: Formula (I) wherein R1, R2, R3, R4, R6

Highly selective recognition of a-chiral primary organoammonium ions by C3-symmetric peptide receptors

Schnopp, Markus,Haberhauer, Gebhard

experimental part, p. 4458 - 4467 (2010/02/16)

A straightforward synthesis of C3-symmet:ric, imidazole-containing, macrocyclic peptides with different binding arms is presented, The chirality of the backbone and the selection of adequate receptor arms make these systems highly selective receptors for α-chiral primary organoammonium ions. Furthermore, the receptors have the ability to discriminate between enantiomeric guests with selectivity ratios of up to 87:13, The binding constants and the selectivity ratios were estimated by standard 1H NMR titration techniques in CDCl3.

Farnesyl protein transferase inhibitors

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, (2008/06/13)

Disclosed are compounds of the formula: wherein R8represents a cyclic moiety to which is bound an imodazolylalkyl group; R9represents a carbamate, urea, amide or sulfonamide group; and the remaining substituents are as defined herein. Also disclosed is a method of treating cancer and a method of inhibiting farnesyl protein transferase using the disclosed compounds.

Azastilbenes. 1. Synthesis, Characterization, and Structure

Vansant, J.,Smets, G.,Declercq, J. P.,Germain, G.,Meerssche, M. Van

, p. 1557 - 1565 (2007/10/02)

The synthesis of several symmetric and asymmetric azastilbenes is described, and their spectral characteristics (NMR, mass, UV, IR) are given.Four of them are new compounds, namely, 1,2-di(4-isoquinolyl)ethylene, 1-(3-pyridyl)-2-(2-pyrazinyl)ethylene, 1-(

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