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1,7-naphthyridin-5(1H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

70730-36-8

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70730-36-8 Usage

Type of compound

Heterocyclic compound

Family

Naphthyridine family

Structure

Contains a nitrogen-containing ring

Applications

a. Building block in the synthesis of pharmaceuticals and organic compounds

Potential biological activities

antibacterial and antifungal properties
c. Investigated for use as an insecticide and herbicide

Importance

a. Unique structure
b. Potential applications in organic chemistry and drug development

Check Digit Verification of cas no

The CAS Registry Mumber 70730-36-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,7,3 and 0 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 70730-36:
(7*7)+(6*0)+(5*7)+(4*3)+(3*0)+(2*3)+(1*6)=108
108 % 10 = 8
So 70730-36-8 is a valid CAS Registry Number.

70730-36-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H-1,7-naphthyridin-5-one

1.2 Other means of identification

Product number -
Other names 5-Hydroxy-1,7-naphthyridin

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:70730-36-8 SDS

70730-36-8Upstream product

70730-36-8Downstream Products

70730-36-8Relevant academic research and scientific papers

PROPANAMINE DERIVATIVES AS SEROTONIN AND NOREPINEPHRINE REUPTAKE INHIBITORS

-

Page 37, (2010/02/07)

There is provided a heretoaryloxy/thio 3-substituted propanamine compound of formula (I) wherein A is selected from -O- and -S-; X is selected from phenyl optionally substituted with up to 5 substituents each independently selected from halo, C1-C4 alkyl and C1-C4 alkoxy, thienyl optionally substituted with up to 3 substituents each independently selected from halo and C1-C4 alkyl, and C2-C8 alkyl, C2-C8 alkenyl, C3-C8 cycloalkyl and C4-C8 cycloalkylalkyl, each of which may be optionally substituted with up to 3 substituents each independently selected from halo, C1-C4 alkyl, C1-C4 alkoxy, C1-C4 alkyl-S(O)n- where n is 0, 1 or 2, -CF3, -CN and -CONH2; Y is selected from dihydrobenzothienyl, benzothiazolyl, benzoisothiazolyl, quinolyl, isoquinolyl, naphthyridyl, and thienopyridyl, each of which may be optionally substituted with up to 4 or, where possible, up to 5 substituents each independently selected from halo, C1-C4 alkyl, C1-C4 alkoxy, C1-C4 alkyl-S(O)n- where n is 0, 1 or 2, nitro, acetyl, -CF3, -SCF3 and cyano; Z is selected from H, OR3 or F, wherein R3 is selected from H, C1-C6 alkyl and phenyl C1-C6 alkyl; R1 and R2 are each independently H or C1-C4 alkyl; and pharmaceutically acceptable salts thereof.

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