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6562-92-1

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6562-92-1 Usage

Description

5-Chloromethyl-2,2,8-trimethyl-4H-1,3-dioxino[4,5-c]pyridine is a chemical compound with the molecular formula C11H15ClNO2. It is a derivative of pyridine and contains a chloromethyl group and a dioxin ring. 5-Chloromethyl-2,2,8-trimethyl-4H-1,3-dioxino[4,5-c]pyridine is characterized by its unique structure, which makes it a valuable intermediate in the synthesis of various complex organic molecules.

Uses

Used in Organic Synthesis:
5-Chloromethyl-2,2,8-trimethyl-4H-1,3-dioxino[4,5-c]pyridine is used as a reagent in organic synthesis for the preparation of various pharmaceuticals, agrochemicals, and fine chemicals. Its versatile structure allows for the creation of a wide range of compounds with diverse applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 5-Chloromethyl-2,2,8-trimethyl-4H-1,3-dioxino[4,5-c]pyridine is used as a key intermediate in the development of new drugs. Its unique structure contributes to the design and synthesis of novel therapeutic agents with potential applications in treating various diseases and conditions.
Used in Agrochemical Industry:
5-Chloromethyl-2,2,8-trimethyl-4H-1,3-dioxino[4,5-c]pyridine is also utilized in the agrochemical industry for the synthesis of various agrochemicals. Its role as an intermediate allows for the development of new compounds that can be used in agriculture to improve crop protection and yield.
Used in Fine Chemicals Production:
In the production of fine chemicals, 5-Chloromethyl-2,2,8-trimethyl-4H-1,3-dioxino[4,5-c]pyridine is employed as a valuable intermediate. Its unique structure enables the synthesis of specialty chemicals used in various industries, such as fragrances, dyes, and coatings.
Used in Antimicrobial and Anti-fungal Applications:
5-Chloromethyl-2,2,8-trimethyl-4H-1,3-dioxino[4,5-c]pyridine has been studied for its potential biological activities, including its antimicrobial and antifungal properties. This makes it a promising candidate for use in applications where control of microbial growth is necessary, such as in medical, food preservation, and water treatment industries.

Check Digit Verification of cas no

The CAS Registry Mumber 6562-92-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,6 and 2 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6562-92:
(6*6)+(5*5)+(4*6)+(3*2)+(2*9)+(1*2)=111
111 % 10 = 1
So 6562-92-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H14ClNO2/c1-7-10-9(8(4-12)5-13-7)6-14-11(2,3)15-10/h5H,4,6H2,1-3H3

6562-92-1SDS

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 5-(chloromethyl)-2,2,8-trimethyl-4H-[1,3]dioxino[4,5-c]pyridine

1.2 Other means of identification

Product number -
Other names 2-(3,4-dihydro-naphthalen-1-yl)-acetic acid ethyl ester

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:6562-92-1 SDS

6562-92-1Relevant articles and documents

INHIBITORS OF THE KYNURENINE PATHWAY

-

, (2014/12/12)

The present application provides novel inhibitors of indoleamine 2,3-dioxygenase-1 and/or indoleamine 2,3-dioxygenase-2 and/or tryptophan 2,3-dioxygenase, metabolites thereof, and phannaceutically acceptable salts or prodrugs thereof. Also provided are methods for preparing these compounds. A therapeutically effective amount of one or more of the compounds of formula (I) is useful in treating diseases resulting from dysregulation of the kynurenine pathway. Compounds of formula (I) act by inhibiting the enzymatic activity or expression of indoleamine 2,3-dioxygenase-1 and/or indoleamine 2,3-dioxygenase-2 and/or tryptophan 2,3-dioxygenase.

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