1415638-13-9 Usage
Description
(5-bromo-1-methyl-1H-pyrazol-4-yl)methanol, also known as 5-bromo-1-methyl-1H-pyrazole-4-carbinol, is a chemical compound characterized by its molecular formula C6H7BrN2O. This white to off-white crystalline powder serves as a crucial building block in the synthesis of a wide range of pharmaceuticals and agrochemicals. As a derivative of pyrazole—a five-membered heterocyclic compound with nitrogen atoms in the ring—the addition of a bromine atom and a methyl group to the pyrazole ring significantly enhances the compound's biological and chemical properties. This enhancement renders (5-bromo-1-methyl-1H-pyrazol-4-yl)methanol a valuable asset in drug discovery and development, with its versatile reactivity and potential applications making it a noteworthy component in the field of medicinal chemistry and organic synthesis.
Uses
Used in Pharmaceutical Industry:
(5-bromo-1-methyl-1H-pyrazol-4-yl)methanol is used as a key intermediate for the development of various pharmaceuticals due to its unique chemical structure and reactivity. Its ability to be incorporated into the synthesis of a broad spectrum of drugs makes it a valuable asset in the creation of novel therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, (5-bromo-1-methyl-1H-pyrazol-4-yl)methanol is utilized as a building block for the synthesis of agrochemicals, such as pesticides and herbicides. Its chemical properties allow for the development of effective compounds that can protect crops and enhance agricultural productivity.
Used in Medicinal Chemistry Research:
(5-bromo-1-methyl-1H-pyrazol-4-yl)methanol is employed as a research compound in medicinal chemistry, where it is investigated for its potential to contribute to the development of new drugs and therapeutic agents. Its unique structure and reactivity make it an attractive candidate for exploring novel chemical pathways and interactions with biological targets.
Used in Organic Synthesis:
As a versatile reagent in organic synthesis, (5-bromo-1-methyl-1H-pyrazol-4-yl)methanol is used to create a variety of complex organic molecules. Its unique functional groups and reactivity enable the formation of diverse chemical products, which can be applied in various industries, including pharmaceuticals, materials science, and specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 1415638-13-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,5,6,3 and 8 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1415638-13:
(9*1)+(8*4)+(7*1)+(6*5)+(5*6)+(4*3)+(3*8)+(2*1)+(1*3)=149
149 % 10 = 9
So 1415638-13-9 is a valid CAS Registry Number.
1415638-13-9Relevant articles and documents
Access and modulation of substituted 1-methyl-1,6-dihydropyrazolo[3,4-c]pyrazoles
Ostache, Nicu-Cosmin,Hiebel, Marie-Aude,F?naru, Adriana-Lumini?a,Allouchi, Hassan,Guillaumet, Gérald,Suzenet, Franck
, p. 9756 - 9765 (2021/03/16)
Despite the pharmacological potential of the pyrazolo[3,4-c]pyrazoles, only a few methods of preparation and direct functionalization of this moiety have been described. We report herein a convenient design of new pyrazolo[3,4-c]pyrazoles with a high therapeutic impact. The effective chosen strategy consists of hydrazine condensations and C-N Ullmann-type cross-coupling reactions with microwave activation. Moreover, chemoselective bromination of the newly formed bipyrazoles followed by Suzuki-Miyaura cross-coupling reactions allowed the synthesis of a variety of modulated heterobicycles.
