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(5-Bromo-4-Methylpyridin-3-yl)Methanol, also known as 5-bromonicotinaldehyde, is a chemical compound characterized by the molecular formula C7H8BrNO. It is a white to off-white solid with a molecular weight of 202.05 g/mol. (5-BroMo-4-Methylpyridin-3-yl)Methanol is recognized for its unique chemical properties and structure, making it a valuable building block in various fields.

351458-17-8

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351458-17-8 Usage

Uses

Used in Organic Synthesis:
(5-Bromo-4-Methylpyridin-3-yl)Methanol is used as a building block in organic synthesis for the creation of various biologically active molecules. Its unique structure allows it to be a key component in the formation of complex organic compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (5-Bromo-4-Methylpyridin-3-yl)Methanol is utilized as an intermediate for the synthesis of pharmaceutical drugs. Its properties contribute to the development of new medications with potential therapeutic applications.
Used in Agrochemical Production:
(5-Bromo-4-Methylpyridin-3-yl)Methanol is also used as an intermediate in the production of agrochemicals. Its role in this industry is crucial for the synthesis of compounds that can be used in agricultural applications to improve crop yields and protect plants from pests.
Used in Dye Manufacturing:
In the dye industry, (5-Bromo-4-Methylpyridin-3-yl)Methanol serves as an intermediate, contributing to the development of new dyes with specific color properties and applications in various sectors, including textiles and printing.
Used in Material Science:
(5-Bromo-4-Methylpyridin-3-yl)Methanol has potential applications in the development of new materials due to its unique chemical characteristics. It can be incorporated into the design and synthesis of advanced materials with specialized properties for use in different industries.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (5-Bromo-4-Methylpyridin-3-yl)Methanol is explored for its potential to contribute to the discovery and design of new drugs. Its structural features make it a promising candidate for the development of pharmaceutical agents with novel mechanisms of action.

Check Digit Verification of cas no

The CAS Registry Mumber 351458-17-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,1,4,5 and 8 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 351458-17:
(8*3)+(7*5)+(6*1)+(5*4)+(4*5)+(3*8)+(2*1)+(1*7)=138
138 % 10 = 8
So 351458-17-8 is a valid CAS Registry Number.

351458-17-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name (5-bromo-4-methylpyridin-3-yl)methanol

1.2 Other means of identification

Product number -
Other names 3-Pyridinemethanol,5-bromo-4-methyl

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:351458-17-8 SDS

351458-17-8Relevant articles and documents

SYNTHESIS OF 5-BROMO-4-METHYL-PYRIDIN-3-YLMETHYL)-ETHYL-CARBAMIC ACID TERT-BUTYL ESTER

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Page/Page column 11-12, (2010/11/08)

The present invention relates to novel synthetic methods for the preparation of intermediates of 3{5-[3-(4,6-Difluoro-1H-benzoimidazol-2-yl)-1H-indazol-5-yl]-4-methyl-pyridin-3-ylmethyl}-ethyl-amine.

Indazolecarboxamide derivatives, preparation and use thereof as CDK1, CDK2 and CDK4 inhibitors

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Page/Page column 15, (2008/06/13)

Compound corresponding to general formula (I): [image] in which, R1 represents a hydrogen or halogen atom, an NH2, NHR2, NHCOR2, NO2, CN, CH2NH2 and CH2NHR2; or alternatively R1 represents an optionally substituted phenyl or an optionally substituted heteroaromatic group; Ar represents an optionally substituted phenyl group or an optionally substituted heteroaromatic group; n represents 0, 1, 2 or 3; in the form of a base, of an addition salt with an acid, of a hydrate or of a solvate. Application in therapy.

Indazole compounds, pharmaceutical compositions, and methods for mediating or inhibiting cell proliferation

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, (2008/06/13)

Indazole compounds that modulate and/or inhibit cell proliferation, such as the activity of protein kinases are described. These compounds and pharmaceutical compositions containing them are capable of mediating, e.g., kinases-dependent diseases to modulate and/or inhibit unwanted cell proliferation. The invention is also directed to the therapeutic or prophylactic use of pharmaceutical compositions containing such compounds, and to methods of treating cancer as well as other disease states associated with unwanted angiogenesis and/or cellular proliferation, such as diabetic retinopathy, neovascular glaucoma, rheumatoid arthritis, and psoriasis, by administering effective amounts of such compounds.

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