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1192813-41-4

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1192813-41-4 Usage

General Description

2-(difluoromethoxy)-5-nitropyridine is a chemical compound that contains a pyridine ring with a difluoromethoxy group at position 2 and a nitro group at position 5. It is an aromatic nitro compound and is used as a building block in the synthesis of various pharmaceuticals and agrochemicals. The difluoromethoxy group provides increased lipophilicity and metabolic stability to the molecule, making it useful in drug design and development. The nitro group can undergo various chemical reactions, making this compound versatile for the creation of different chemical structures. Overall, 2-(difluoromethoxy)-5-nitropyridine has potential applications in the pharmaceutical and agrochemical industries due to its unique chemical properties.

Check Digit Verification of cas no

The CAS Registry Mumber 1192813-41-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,2,8,1 and 3 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1192813-41:
(9*1)+(8*1)+(7*9)+(6*2)+(5*8)+(4*1)+(3*3)+(2*4)+(1*1)=154
154 % 10 = 4
So 1192813-41-4 is a valid CAS Registry Number.

1192813-41-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(difluoromethoxy)-5-nitropyridine

1.2 Other means of identification

Product number -
Other names 2-difluoromethoxy-5-nitro-pyridine

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:1192813-41-4 SDS

1192813-41-4Relevant articles and documents

5-HETEROARYL SUBSTITUTED INDAZOLE-3-CARBOXAMIDES AND PREPARATION AND USE THEREOF

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Paragraph 0750; 0751, (2019/09/06)

Indazole compounds for treating various diseases and pathologies are disclosed. More particularly, the present disclosure concerns the use of an indazole compound or analogs thereof, in the treatment of disorders characterized by the activation of Wnt pathway signaling (e.g., tendinopathy, dermatitis, psoriasis, morphea, ichthyosis, Raynaud's syndrome, Darier's disease, scleroderma, cancer, abnormal cellular proliferation, angiogenesis, Alzheimer's disease, lung disease, and osteoarthritis), the modulation of cellular events mediated by Wnt pathway signaling, as well as neurological conditions/disorders/diseases linked to overexpression of DYRK1A.

Tricyclic Compounds As mPGES-1 Inhibitors

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Page/Page column 34, (2012/05/07)

The present invention relates to tricyclic compounds of formula (I) or pharmaceutically acceptable salt thereof as mPGES-1 inhibitors. These compounds are inhibitors of the microsomal prostaglandin E synthase-1 (mPGES-1) enzyme and are therefore useful in the treatment of pain and/or inflammation from a variety of diseases or conditions, such as asthma, osteoarthritis, rheumatoid arthritis, acute or chronic pain and neurodegenerative diseases.

QUINUCLIDINE COMPOUNDS AS ALPHA-7 NICOTINIC ACETYLCHOLINE RECEPTOR LIGANDS

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Page/Page column 140, (2011/05/11)

The disclosure provides compounds of formula I, including their salts, as well as compositions and methods of using the compounds. The compounds are ligands for the nicotinic 7 receptor and may be useful for the treatment of various disorders of the central nervous system, especially affective and neurodegenerative disorders.

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