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24306-75-0

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24306-75-0 Usage

Abbreviation

TFPy-3-CHO

Physical State

Yellow liquid

Odor

Strong, pungent

Primary Use

Intermediate in pharmaceutical and agrochemical synthesis

Secondary Use

Building block in fine chemicals production

Reactivity

Highly reactive

Handling

Requires careful handling due to potential irritation to skin, eyes, and respiratory system

Safety Precautions

Must be stored and handled according to proper safety protocols

Hazardous Properties

Combustible

Check Digit Verification of cas no

The CAS Registry Mumber 24306-75-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,3,0 and 6 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 24306-75:
(7*2)+(6*4)+(5*3)+(4*0)+(3*6)+(2*7)+(1*5)=90
90 % 10 = 0
So 24306-75-0 is a valid CAS Registry Number.

24306-75-0SDS

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 2,4,5,6-tetrafluoropyridine-3-carbaldehyde

1.2 Other means of identification

Product number -
Other names 24,5,6-Tetrafluoropyridine-3-carboxaldehyde

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:24306-75-0 SDS

24306-75-0Downstream Products

24306-75-0Relevant articles and documents

Preparation and reactions of 2,3,4,6-tetrafluoropyridine and its derivatives

Coe, Paul L.,Rees, Anthony J.

, p. 45 - 60 (2007/10/03)

A reliable route to 2,3,4,6-tetrafluoropyridine has been established starting from the readily available 3,5-dichlorotrifluoropyridine by halogen exchange under controlled conditions to give 3-chlorotetrafluoropyridine and its subsequent hydrodechlorination using hydrogen over palladium on alumina at 250-270°C. The formation and reactions of the 3-lithio derivative have been studied with the aim of obtaining 3,4-disubstituted trifluoropyridines. Routes to such materials have been developed and their conversion to deazapurine derivatives as potential substrates for the generation of anti-sense nucleosides are reported.

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