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1,8-Naphthyridin-2(1H)-one, 4-(4-Methylphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

127446-47-3

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127446-47-3 Usage

Medicinal Use

Treatment of rheumatoid arthritis, psoriatic arthritis, and ulcerative colitis

Mechanism of Action

Janus kinase (JAK) inhibitor

Enzyme Inhibition

Blocks certain enzymes involved in the immune system and inflammation

Effect on Inflammatory Conditions

Reduces symptoms and progression of the diseases

Pharmaceutical Form

Tablet

Prescription

Typically prescribed by a healthcare professional

Chronic Inflammatory Disease Management

Used for managing chronic inflammatory diseases

Check Digit Verification of cas no

The CAS Registry Mumber 127446-47-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,4,4 and 6 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 127446-47:
(8*1)+(7*2)+(6*7)+(5*4)+(4*4)+(3*6)+(2*4)+(1*7)=133
133 % 10 = 3
So 127446-47-3 is a valid CAS Registry Number.

127446-47-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(4-methylphenyl)-1H-1,8-naphthyridin-2-one

1.2 Other means of identification

Product number -
Other names -

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:127446-47-3 SDS

127446-47-3Downstream Products

127446-47-3Relevant academic research and scientific papers

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

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