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92643-16-8

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92643-16-8 Usage

Description

6-BROMO-1-(CHLOROMETHYL)-2-METHOXYNAPHTHALENE is a chemical compound with a molecular formula of C11H9BrClO. It is a derivative of naphthalene, featuring a bromo, chloromethyl, and methoxy group. 6-BROMO-1-(CHLOROMETHYL)-2-METHOXYNAPHTHALENE is recognized for its reactivity in various organic reactions and serves as a valuable building block for synthesizing more complex organic compounds. Due to potential health and environmental risks, it is crucial to handle this chemical with care.

Uses

Used in Organic Synthesis:
6-BROMO-1-(CHLOROMETHYL)-2-METHOXYNAPHTHALENE is used as a key intermediate in organic synthesis for the creation of more complex organic compounds. Its unique structure, which includes a bromo and chloromethyl group along with a methoxy group, allows it to participate in a wide range of organic reactions, making it a versatile component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Research:
In the field of research, 6-BROMO-1-(CHLOROMETHYL)-2-METHOXYNAPHTHALENE is utilized as a model compound to study various organic reactions and mechanisms. Its reactivity and structural features make it an ideal candidate for exploring new synthetic pathways and developing innovative methodologies in organic chemistry.
Used in Pharmaceutical Industry:
6-BROMO-1-(CHLOROMETHYL)-2-METHOXYNAPHTHALENE is used as a building block in the pharmaceutical industry for the development of new drugs. Its ability to react in various organic reactions allows chemists to create diverse drug candidates with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, 6-BROMO-1-(CHLOROMETHYL)-2-METHOXYNAPHTHALENE is employed as a starting material for the synthesis of new agrochemicals. Its reactivity and structural features enable the development of novel compounds with improved pesticidal properties.
Used in Specialty Chemicals:
6-BROMO-1-(CHLOROMETHYL)-2-METHOXYNAPHTHALENE is used as a precursor in the production of specialty chemicals, such as dyes, fragrances, and other fine chemicals. Its unique structure and reactivity contribute to the creation of high-value products with specific applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 92643-16-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,6,4 and 3 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 92643-16:
(7*9)+(6*2)+(5*6)+(4*4)+(3*3)+(2*1)+(1*6)=138
138 % 10 = 8
So 92643-16-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H10BrClO/c1-15-12-5-2-8-6-9(13)3-4-10(8)11(12)7-14/h2-6H,7H2,1H3

92643-16-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-BROMO-1-(CHLOROMETHYL)-2-METHOXYNAPHTHALENE

1.2 Other means of identification

Product number -
Other names (6-Brom-1-chlormethyl-[2]naphthyl)-methyl-aether

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:92643-16-8 SDS

92643-16-8Relevant articles and documents

(PIPERIDIN-3-YL)(NAPHTHALEN-2-YL)METHANONE DERIVATIVES AND RELATED COMPOUNDS AS INHIBITORS OF THE HISTONE DEMETHYLASE KDM2B FOR THE TREATMENT OF CANCER

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Page/Page column 133, (2016/08/10)

The present invention relates to (piperidin-3-yl)(naphthalen-2-yl) methanone derivatives and related compounds as inhibitors of one or more histone demethylses, such as KDM2b. The invention also provides pharmaceutically acceptable compositions comprising

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