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5-chloro-2-(difluoroMethoxy)pyridine is a pyridine derivative with the molecular formula C6H3ClF2NO. It features a chlorine atom at the 5th position and two difluoromethoxy groups at the 2nd position, making it a versatile intermediate in various chemical syntheses.

1214323-40-6

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1214323-40-6 Usage

Uses

Used in Pharmaceutical Industry:
5-chloro-2-(difluoroMethoxy)pyridine is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
5-chloro-2-(difluoroMethoxy)pyridine also serves as an intermediate in the production of agrochemicals, contributing to the development of pesticides and other agricultural products to enhance crop protection and yield.
Used in Dye Manufacturing:
5-chloro-2-(difluoroMethoxy)pyridine is utilized in the manufacturing of dyes, where its specific chemical properties contribute to the creation of a range of colorants for different industries.
Used as a Solvent in Organic Synthesis:
Due to its solubility and reactivity properties, 5-chloro-2-(difluoroMethoxy)pyridine is employed as a solvent in organic synthesis, facilitating various chemical reactions in research and industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1214323-40-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,4,3,2 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1214323-40:
(9*1)+(8*2)+(7*1)+(6*4)+(5*3)+(4*2)+(3*3)+(2*4)+(1*0)=96
96 % 10 = 6
So 1214323-40-6 is a valid CAS Registry Number.

1214323-40-6SDS

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 5-Chloro-2-(difluoromethoxy)pyridine

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:1214323-40-6 SDS

1214323-40-6Relevant articles and documents

Use of fluoroform as a source of difluorocarbene in the synthesis of N-CF2H heterocycles and difluoromethoxypyridines

Thomoson, Charles S.,Wang, Linhua,Dolbier, William R.

, p. 34 - 39 (2015/03/04)

Fluoroform is used as a source of difluorocarbene to convert various N-, O-, and C-nucleophiles to their difluoromethylated derivatives. Imidazole, benzimidazole, benztriazole, hydroxypyridines, and their derivatives underwent reaction at moderate temperatures and atmospheric pressure, using potassium hydroxide as base in a two-phase (water/acetonitrile) process to provide moderate to good yields of the respective products. Nitrophenols required addition of a co-solvent (methanol) to obtain good yields of products.

HETEROCYCLIC COMPOUNDS AND THEIR USE AS INHIBITORS OF PI3K ACTIVITY

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Page/Page column 226, (2012/01/15)

Substituted bicyclic heteroaryls and compositions containing them, for the treatment of general inflammation, arthritis, rheumatic diseases, osteoarthritis, inflammatory bowel disorders, inflammatory eye disorders, inflammatory or unstable bladder disorders, psoriasis, skin complaints with inflammatory components, chronic inflammatory conditions, including but not restricted to autoimmune diseases such as systemic lupus erythematosis (SLE), myestenia gravis, rheumatoid arthritis, acute disseminated encephalomyelitis, idiopathic thrombocytopenic purpura, multiples sclerosis, Sjoegren's syndrome and autoimmune hemolytic anemia, allergic conditions including all forms of hypersensitivity, The present invention also enables methods for treating cancers that are mediated, dependent on or associated with p110 activity, including but not restricted to leukemias, such as Acute Myeloid leukaemia (AML) Myelo-dysplastic syndrome (MDS) myelo-proliferative diseases (MPD) Chronic Myeloid Leukemia (CML) T-cell Acute Lymphoblastic leukaemia ( T-ALL) B-cell Acute Lymphoblastic leukaemia (B-ALL) Non Hodgkins Lymphoma (NHL) B-cell lymphoma and solid tumors, such as breast cancer.

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