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83067-94-1

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83067-94-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83067-94-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,0,6 and 7 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 83067-94:
(7*8)+(6*3)+(5*0)+(4*6)+(3*7)+(2*9)+(1*4)=141
141 % 10 = 1
So 83067-94-1 is a valid CAS Registry Number.

83067-94-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-oxo-1,4-dihydro-[1,5]naphthyridin-3-yl carboxylic acid ethyl ester

1.2 Other means of identification

Product number -
Other names 4-oxo-1,4-dihydro-[1,5]naphthyridine-3-carboxylic 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:83067-94-1 SDS

83067-94-1Relevant articles and documents

NAPHTHYRIDINONE DERIVATIVES AND THEIR USE IN THE TREATMENT, AMELIORATION OR PREVENTION OF A VIRAL DISEASE

-

, (2014/07/22)

The present invention relates to a compound having the general formula (V), optionally in the form of a pharmaceutically acceptable salt, solvate, polymorph, codrug, cocrystal, prodrug, tautomer, racemate, enantiomer, or diastereomer or mixture thereof, which are useful in treating, ameloriating or preventing a viral disease. Furthermore, specific combination therapies are disclosed.

Synthesis and structure-activity relationship studies of dihydronaphthyridinediones as a novel structural class of potent and selective PDE7 inhibitors

Gewald, Rainer,Rueger, Carla,Grunwald, Christian,Egerland, Ute,Hoefgen, Norbert

, p. 6652 - 6656 (2011/12/04)

The synthesis and SAR studies of a series of structurally novel inhibitors of PDE7 are discussed. The best compounds from the series display low nanomolar inhibitory activity and are selective versus other PDE isoenzymes.

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