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2-Fluoro-5-Iodo-3-Picoline, with the molecular formula C6H4FIN2, is a specialized chemical compound that is most commonly known for its application in the domain of organic synthesis. It serves as an essential component in the formation of numerous other complex chemical substances. Due to its unique combination of fluorine and iodine atoms, 2-Fluoro-5-Iodo-3-Picoline demonstrates distinctive chemical behavior that is leveraged in different chemical reactions.

205245-17-6

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205245-17-6 Usage

Uses

Used in Organic Synthesis:
2-Fluoro-5-Iodo-3-Picoline is used as a key component in the synthesis of various complex chemical substances. Its distinctive chemical behavior, resulting from the combination of fluorine and iodine atoms, makes it a valuable asset in the creation of new compounds.
Used in Pharmaceutical Production:
2-Fluoro-5-Iodo-3-Picoline is used as a precursor in the production of pharmaceuticals. Its role in organic synthesis allows for the development of new drug molecules, contributing to advancements in medicine and healthcare. 2-FLUORO-5-IODO-3-PICOLINE is primarily utilized in laboratory settings, where its unique properties can be harnessed to create novel pharmaceutical agents.

Check Digit Verification of cas no

The CAS Registry Mumber 205245-17-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,5,2,4 and 5 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 205245-17:
(8*2)+(7*0)+(6*5)+(5*2)+(4*4)+(3*5)+(2*1)+(1*7)=96
96 % 10 = 6
So 205245-17-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H5FIN/c1-4-2-5(8)3-9-6(4)7/h2-3H,1H3

205245-17-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-fluoro-5-iodo-3-methylpyridine

1.2 Other means of identification

Product number -
Other names 2-Fluoro-5-iodo-3-picoline

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:205245-17-6 SDS

205245-17-6Downstream Products

205245-17-6Relevant academic research and scientific papers

TAU-PROTEIN TARGETING COMPOUNDS AND ASSOCIATED METHODS OF USE

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Paragraph 1007; 1008, (2021/02/12)

The present disclosure relates to bifunctional compounds, which find utility as modulators of tan protein. In particular, the present disclosure is directed to bifunctional compounds, which contain on one end a VHL or cereblon ligand which binds to the E3 ubiquitin ligase and on the other end a moiety which binds tan protein, such that tan protein is placed in proximity to the ubiquitin ligase to effect degradation (and inhibition) of tan. The present disclosure exhibits a broad range of pharmacological activities associated with degradation/inhibition of tan protein. Diseases or disorders that result from aggregation or accumulation of tan protein are treated or prevented with compounds and compositions of the present disclosure.

TAU-PROTEIN TARGETING PROTACS AND ASSOCIATED METHODS OF USE

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Paragraph 1293; 1294, (2018/05/24)

The present disclosure relates to bifunctional compounds, which find utility as modulators of tau protein. In particular, the present disclosure is directed to bifunctional compounds, which contain on one end a VHL or cereblon ligand which binds to the E3 ubiquitin ligase and on the other end a moiety which binds tau protein, such that tau protein is placed in proximity to the ubiquitin ligase to effect degradation (and inhibition) of tau. The present disclosure exhibits a broad range of pharmacological activities associated with degradation/inhibition of tau protein. Diseases or disorders that result from aggregation or accumulation of tau protein are treated or prevented with compounds and compositions of the present disclosure.

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