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1,6-Naphthyridin-5(1H)-one,2,3,4,6-tetrahydro-(9CI), also known as 2,3,4,6-tetrahydro-1,6-naphthyridin-5(1H)-one, is a heterocyclic compound with a molecular formula of C9H9NO. It is a derivative of pyridine and features a six-membered ring fused to a pyridine ring. 1,6-Naphthyridin-5(1H)-one,2,3,4,6-tetrahydro-(9CI) has a wide range of industrial and research applications, making it a valuable building block in the synthesis of pharmaceuticals and agricultural chemicals. Its unique structure and properties also contribute to its use in the development of new materials and as a reagent in organic chemical reactions. Furthermore, it is a subject of interest in scientific research for potential new applications in diverse fields.

155057-98-0

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155057-98-0 Usage

Uses

Used in Pharmaceutical Industry:
1,6-Naphthyridin-5(1H)-one,2,3,4,6-tetrahydro-(9CI) is used as a building block in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs with potential therapeutic properties.
Used in Agricultural Chemicals Industry:
In the agricultural chemicals industry, 1,6-Naphthyridin-5(1H)-one,2,3,4,6-tetrahydro-(9CI) is utilized as a component in the creation of new agrochemicals, potentially enhancing crop protection and yield.
Used in Material Science:
1,6-Naphthyridin-5(1H)-one,2,3,4,6-tetrahydro-(9CI) is employed in the development of new materials due to its unique structural and chemical properties, which may offer novel functionalities and improvements in existing materials.
Used as a Reagent in Organic Chemical Reactions:
1,6-Naphthyridin-5(1H)-one,2,3,4,6-tetrahydro-(9CI) serves as a reagent in various organic chemical reactions, facilitating specific transformations and syntheses that are otherwise challenging to achieve.
Used in Scientific Research:
In the realm of scientific research, 1,6-Naphthyridin-5(1H)-one,2,3,4,6-tetrahydro-(9CI) is explored for its potential new applications across diverse fields, driven by its distinctive structure and properties that may lead to innovative discoveries and technologies.

Check Digit Verification of cas no

The CAS Registry Mumber 155057-98-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,0,5 and 7 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 155057-98:
(8*1)+(7*5)+(6*5)+(5*0)+(4*5)+(3*7)+(2*9)+(1*8)=140
140 % 10 = 0
So 155057-98-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H10N2O/c11-8-6-2-1-4-9-7(6)3-5-10-8/h3,5,9H,1-2,4H2,(H,10,11)

155057-98-0SDS

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 2,3,4,6-tetrahydro-1H-1,6-naphthyridin-5-one

1.2 Other means of identification

Product number -
Other names 1,2,3,4-TETRAHYDRO-1,6-NAPHTHYRIDIN-5-OL

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:155057-98-0 SDS

155057-98-0Downstream Products

155057-98-0Relevant articles and documents

Ready access to 7,8-dihydro- and 1,2,3,4-tetrahydro-1,6-naphthyridine-5(6H) -ones from simple pyridine precursors

Showalter, H. D. Hollis

, p. 1311 - 1317 (2007/10/03)

Short pathways are described for the synthesis of a representative example of each of the 7,8-dihydro- and 1,2,3,4-tetrahydro-1,6-naphthyridine-5(6H)-one ring systems from simple pyridine precursors. An attempted synthesis of the related 4,6-dihydro-1,6-naphthyridin-5(1H)-one ring system from a common intermediate was unsuccessful.

Dihydro- and tetrahydronaphthyridines

-

, (2008/06/13)

This invention concerns novel dihydro- and tetrahydronaphthyridines useful for enhancing the lethal effects on tumor cells to treatment causing DNA-damaging activity as with ionizing radiation or with a chemotherapeutic agent.

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