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2,3-difluoroisonicotinonitrile is a heterocyclic chemical compound with the molecular formula C6H2F2N2. It is a derivative of isonicotinonitrile and is an important building block in the synthesis of various pharmaceutical and agrochemical products. This colorless, solid compound has a slightly sweet smell and is soluble in organic solvents such as ethanol, acetone, and dimethyl sulfoxide.

1210041-67-0

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1210041-67-0 Usage

Uses

Used in Pharmaceutical Industry:
2,3-difluoroisonicotinonitrile is used as a reagent for the production of various pharmaceuticals. It serves as a key intermediate in the synthesis of drugs, contributing to the development of new medications.
Used in Agrochemical Industry:
2,3-difluoroisonicotinonitrile is used as a reagent in the production of agrochemicals. It plays a crucial role in the synthesis of pesticides and other agricultural chemicals, enhancing crop protection and yield.
Used in Organic Synthesis:
2,3-difluoroisonicotinonitrile is used as a reagent in organic synthesis. Its versatility in chemical reactions makes it a valuable component in the creation of a wide range of organic compounds.
Used in Chemical Industry:
Due to its low toxicity and wide applicability, 2,3-difluoroisonicotinonitrile is an important intermediate in the chemical industry. It is utilized in various chemical processes to produce a broad spectrum of products.

Check Digit Verification of cas no

The CAS Registry Mumber 1210041-67-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,0,0,4 and 1 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1210041-67:
(9*1)+(8*2)+(7*1)+(6*0)+(5*0)+(4*4)+(3*1)+(2*6)+(1*7)=70
70 % 10 = 0
So 1210041-67-0 is a valid CAS Registry Number.

1210041-67-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-difluoroisonicotinonitrile

1.2 Other means of identification

Product number -
Other names 2,3-difluoropyridine-4-carbonitrile

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:1210041-67-0 SDS

1210041-67-0Downstream Products

1210041-67-0Relevant academic research and scientific papers

3-ARYL AND HETEROARYL SUBSTITUTED 5-TRIFLUOROMETHYL OXADIAZOLES AS HISTONE DEACETYLASE 6 (HDAC6) INHIBITORS

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Page/Page column 159, (2018/04/11)

The present invention is directed to substituted 5-trifluoromethyl oxadiazole compounds of generic formula (I) or a pharmaceutically acceptable salt thereof. In particular, the invention is directed to a class of aryl and heteroaryl substituted 5-trifluoromethyl oxadiazole compounds of formula I which may be useful as HDAC6 inhibitors for treating cellular proliferative diseases, including cancer, neurodegenerative diseases, such as schizophrenia and stroke, as well as other diseases.

3- HETEROARYL SUBSTITUTED 5-TRIFLUOROMETHYL OXADIAZOLES AS HISTONE DEACETYLASE 6 (HDAC6) INHIBITORS

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Page/Page column 42, (2018/04/11)

The present invention is directed to substituted 5-trifluoromethyl oxadiazole compounds of generic formula (I) (I) or a pharmaceutically acceptable salt thereof. In particular, the invention is directed to a class of heteroaryl substituted 5-trifluoromethyl oxadiazole compounds of formula I which may be useful as HDAC6 inhibitors for treating cellular proliferative diseases, including cancer, neurodegenerative diseases, such as schizophrenia and stroke, as well as other diseases.

Pyridines substituted with five different elements

Vonkieseritzky, Fredrik,Lindstrm, Johan

experimental part, p. 63 - 66 (2010/04/26)

By stepwise and regioselective installation of functional groups, we have synthesized and characterized two pyridines, 3-fluoro-5-iodo-2-(methylthio)-6-(trimethylsilyl)isonicotinonitrile and 3-fluoro-5-iodo-2-methoxy-6-(trimethylsilyl)isonicotinonitrile,

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