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6-CHLORO-1,7-NAPHTHYRIDIN-2(1H)-ONE is a chloro-substituted heterocyclic compound with the molecular formula C11H7ClN2O. It features a naphthyridine core and a ketone functional group, making it a valuable building block in the synthesis of pharmaceuticals and agrochemicals. Its potential biological activities and applications in the development of anti-infective and anti-cancer agents highlight its significance in the field of medicinal chemistry.

93493-68-6

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93493-68-6 Usage

Uses

Used in Pharmaceutical Industry:
6-CHLORO-1,7-NAPHTHYRIDIN-2(1H)-ONE is used as a key intermediate in the synthesis of various pharmaceuticals for its potential biological activities. It plays a crucial role in the development of new drugs, particularly in the field of anti-infective and anti-cancer agents, due to its unique chemical structure and properties.
Used in Agrochemical Industry:
In the agrochemical industry, 6-CHLORO-1,7-NAPHTHYRIDIN-2(1H)-ONE is utilized as a precursor in the production of agrochemicals with potential pesticidal or herbicidal properties. Its chemical structure allows for the creation of compounds that can effectively target and control pests or weeds, contributing to improved crop protection and yield.
Used in Organic Synthesis:
6-CHLORO-1,7-NAPHTHYRIDIN-2(1H)-ONE serves as an important intermediate in organic synthesis for the production of other valuable chemicals. Its versatility in chemical reactions enables the synthesis of a wide range of compounds with diverse applications, including specialty chemicals, dyes, and other industrial products.

Check Digit Verification of cas no

The CAS Registry Mumber 93493-68-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,4,9 and 3 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 93493-68:
(7*9)+(6*3)+(5*4)+(4*9)+(3*3)+(2*6)+(1*8)=166
166 % 10 = 6
So 93493-68-6 is a valid CAS Registry Number.

93493-68-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-chloro-1H-1,7-naphthyridin-2-one

1.2 Other means of identification

Product number -
Other names 6-chloranyl-1H-1,7-naphthyridin-2-one

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:93493-68-6 SDS

93493-68-6Downstream Products

93493-68-6Relevant academic research and scientific papers

PESTICIDALLY ACTIVE HETEROCYCLIC DERIVATIVES WITH SULFUR CONTAINING SUBSTITUENTS

-

, (2021/07/10)

Compounds of the formula (I) wherein the substituents are as defined in claim 1. Furthermore, the present invention relates to agrochemical compositions which comprise compounds of formula (I), to preparation of these compositions, and to the use of the compounds or compositions in agriculture or horticulture for combating, preventing or controlling animal pests, including arthropods and in particular insects, nematodes, molluscs or representatives of the order Acarina.

A General Approach to the Synthesis of 1,6-, 1,7-, and 1,8-Naphthyridines

Turner, James A.

, p. 4744 - 4750 (2007/10/02)

A new three-step procedure for pyridine annulation is described and illustrated with efficient syntheses of various 1,6-, 1,7-, and 1,8-naphthyridin-2-ones as well as 6-chloroquinolin-2-one.The regiospecific ortho metalation and subsequent formylation of

Naphthyridinyloxy(or thio)phenoxy propanoic acids, derivatives thereof and methods of herbicidal use

-

, (2008/06/13)

Novel 2-naphthyridinyloxy(or thio)phenoxy propanoic acid compounds of the formula STR1 wherein STR2 represents a 6 membered nitrogen containing an aromatic ring which forms a 1,5-, 1,6-, 1,7- or 1,8-naphthyridinyl moiety with the adjoining pyridine ring,

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