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5-(Bromomethyl)-1-methyl-1H-1,2,3-benzotriazole is a chemical compound characterized by the molecular formula C8H8N3Br. It is a derivative of benzotriazole, known for its utility as a corrosion inhibitor and UV stabilizer. The incorporation of a bromomethyl group in this molecule enhances its reactivity, allowing for nucleophilic substitution reactions that facilitate the introduction of the benzotriazole moiety into more complex organic structures. The presence of a methyl group and the benzotriazole scaffold also endows 5-(Bromomethyl)-1-methyl-1H-1,2,3-benzotriazole with the potential to function as a ligand in coordination chemistry, broadening its applications in the synthesis of metal complexes. This versatile chemical has a wide range of potential uses across various chemical and industrial processes.

499770-76-2

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499770-76-2 Usage

Uses

Used in Organic Synthesis:
5-(Bromomethyl)-1-methyl-1H-1,2,3-benzotriazole is utilized as a synthetic intermediate for the creation of more complex organic molecules. Its bromomethyl group is particularly useful for nucleophilic substitution reactions, allowing chemists to incorporate the benzotriazole moiety into larger molecular structures for various applications.
Used in Corrosion Inhibition:
In the chemical industry, 5-(Bromomethyl)-1-methyl-1H-1,2,3-benzotriazole serves as a corrosion inhibitor, protecting metal surfaces from degradation and extending the lifespan of equipment and structures.
Used in UV Stabilization:
5-(Bromomethyl)-1-methyl-1H-1,2,3-benzotriazole is also employed as a UV stabilizer in various applications, such as in the production of plastics and coatings, to prevent degradation caused by exposure to ultraviolet radiation.
Used in Coordination Chemistry:
5-(Bromomethyl)-1-methyl-1H-1,2,3-benzotriazole is used as a ligand in coordination chemistry, enabling the synthesis of metal complexes with potential applications in catalysis, materials science, and other specialized fields.
Used in Pharmaceutical and Agrochemical Industries:
5-(Bromomethyl)-1-methyl-1H-1,2,3-benzotriazole may also find use in the development of pharmaceuticals and agrochemicals, where the benzotriazole moiety can be incorporated into active molecules to enhance their properties or to create new therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 499770-76-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,9,9,7,7 and 0 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 499770-76:
(8*4)+(7*9)+(6*9)+(5*7)+(4*7)+(3*0)+(2*7)+(1*6)=232
232 % 10 = 2
So 499770-76-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H8BrN3/c1-12-8-3-2-6(5-9)4-7(8)10-11-12/h2-4H,5H2,1H3

499770-76-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(Bromomethyl)-1-methyl-1H-benzo[d][1,2,3]triazole

1.2 Other means of identification

Product number -
Other names 5-(Bromomethyl)-1-methyl-1H-1,2,3-benzotriazole

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:499770-76-2 SDS

499770-76-2Downstream Products

499770-76-2Relevant academic research and scientific papers

USE OF PYRROLO [2 , 3-B] PYRIDINES TO PREPARE A MEDICAMENT FOR TREATING PAIN

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Page/Page column 62-63, (2008/06/13)

There are provided according to the invention compounds of formula (I), in free or salt form, wherein R1, R2, R3, R4, R5, R6, Q, W, X, m, n and p are as described in the specification, process for preparing them, and their use in the manufacture of a medicament for the treatment of neuropathic pain.

ORGANIC COMPOUNDS

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Page/Page column 67-68, (2010/02/15)

There are provided according to the invention compounds of formula (I), in free or salt form, wherein R1, R2, R3, R4, R5, R6, Q, W, X, m, n and p are as described in the specification, process for preparing them, and their use as pharmaceuticals.

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