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(3-bromo-5-methylphenyl)methanol is a chemical compound that features a benzene ring with a bromine atom at the 3rd position and a methyl group at the 5th position. Additionally, it has a hydroxyl group (-OH) attached to the carbon atom next to the benzene ring. This structure endows the compound with unique properties, making it a valuable intermediate in various chemical processes.

648439-19-4

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648439-19-4 Usage

Uses

Used in Organic Synthesis:
(3-bromo-5-methylphenyl)methanol serves as a versatile building block in organic synthesis, contributing to the creation of a diverse array of chemical products. Its unique structure allows it to be a key component in the synthesis of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, (3-bromo-5-methylphenyl)methanol is utilized as an intermediate for the synthesis of various drugs. Its specific functional groups and structural features make it suitable for the development of new medicinal compounds with potential therapeutic applications.
Used in Agrochemical Production:
(3-broMo-5-Methylphenyl)Methanol also finds application in the agrochemical industry, where it is used in the synthesis of pesticides, herbicides, and other agricultural chemicals. Its role in these processes is crucial for the development of effective and targeted agrochemical products.
Used in Fragrance Production:
(3-bromo-5-methylphenyl)methanol is employed in the production of fragrances, where its unique aromatic properties contribute to the creation of distinct scents for various applications, including perfumes, cosmetics, and other scented products.
Used in Specialty Chemicals Manufacturing:
Furthermore, the compound is used in the manufacturing of specialty chemicals, which are tailored for specific industries and applications. Its versatility and functional groups make it an essential intermediate in the production of these specialized chemical products.

Check Digit Verification of cas no

The CAS Registry Mumber 648439-19-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,4,8,4,3 and 9 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 648439-19:
(8*6)+(7*4)+(6*8)+(5*4)+(4*3)+(3*9)+(2*1)+(1*9)=194
194 % 10 = 4
So 648439-19-4 is a valid CAS Registry Number.

648439-19-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-bromo-5-methylphenyl)methanol

1.2 Other means of identification

Product number -
Other names 3-bromo-5-methylbenzyl alcohol

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:648439-19-4 SDS

648439-19-4Relevant academic research and scientific papers

Method for preparation of aromatic alcohol by photocatalysis of aromatic aldehyde conversion

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Paragraph 0061-0063, (2020/04/17)

The invention relates to a method for preparation of aromatic alcohol by photocatalysis of aromatic aldehyde conversion. By means of a photocatalyst, under the conditions of illumination and inert gas, fatty alcohol is adopted as a proton donor for reduction reaction on aromatic aldehyde to obtain corresponding aromatic alcohol. Fatty alcohol is used as the proton donor, and light energy is used as the energy source to promote high-conversion-rate and high-selectivity synthesis of a series of aromatic alcohol compounds from aromatic aldehyde, the method has universal applicability, and is expected to realize industrial production; and the reaction process is green and environment-friendly, low in cost, easy to operate, short in reaction period, high in conversion rate and good in selectivity.

Insight into the complete substrate-binding pocket of ThiT by chemical and genetic mutations

Swier,Monjas,Ree?ing,Oudshoorn,Aisyah,Primke,Bakker,Van Olst,Ritschel,Faustino,Marrink,Hirsch,Slotboom

supporting information, p. 1121 - 1130 (2017/07/12)

Energy-coupling factor (ECF) transporters are involved in the uptake of micronutrients in bacteria. The transporters capture the substrate by high-affinity binding proteins, the so-called S-components. Here, we present the analysis of two regions of the s

PYRIDONE DERIVATIVES AS NON-NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITORS

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Page/Page column 80, (2010/04/03)

The present invention relates to 2-pyridone derivatives of Formula (I) or (IV) as herein described, compositions containing such compounds, synthetic processes for making such compounds, and therapeutic methods that include the administration of such comp

DUAL PHARMACOPHORES - PDE4-MUSCARINIC ANTAGONISTICS

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, (2009/10/09)

The present invention is directed to novel compounds of Formula's (I) - (VI), and pharmaceutically acceptable salts thereof, pharmaceutical compositions and their use in therapy, for example as inhibitors of phosphodiesterase type IV (PDE4) and as antagonists of muscarinic acetylcholine receptors (mAChRs), in the treatment of and/or prophylaxis of respiratory diseases, including inflammatory and/or allergic diseases such as chronic obstructive pulmonary disease (COPD), asthma, rhinitis (e.g. allergic rhinitis), atopic dermatitis or psoriasis.

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