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3,4,4,4-TETRAFLUORO-3-TRIFLUOROMETHYL-1-BUTYNE, with the molecular formula C6H2F7, is a highly fluorinated and substituted alkyne. It features both fluorine and trifluoromethyl functional groups, making it a versatile and important intermediate in organic synthesis.

24690-53-7

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24690-53-7 Usage

Uses

Used in Pharmaceutical Industry:
3,4,4,4-TETRAFLUORO-3-TRIFLUOROMETHYL-1-BUTYNE is used as a building block in the synthesis of pharmaceuticals due to its high reactivity and ability to participate in various chemical reactions, contributing to the development of complex organic compounds for medicinal applications.
Used in Agrochemical Industry:
Similarly, in the agrochemical sector, 3,4,4,4-TETRAFLUORO-3-TRIFLUOROMETHYL-1-BUTYNE serves as a key intermediate for the production of agrochemicals, leveraging its unique structure and properties to create effective compounds for agricultural use.

Check Digit Verification of cas no

The CAS Registry Mumber 24690-53-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,6,9 and 0 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 24690-53:
(7*2)+(6*4)+(5*6)+(4*9)+(3*0)+(2*5)+(1*3)=117
117 % 10 = 7
So 24690-53-7 is a valid CAS Registry Number.
InChI:InChI=1/C5HF7/c1-2-3(6,4(7,8)9)5(10,11)12/h1H

24690-53-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4,4,4-tetrafluoro-3-(trifluoromethyl)but-1-yne

1.2 Other means of identification

Product number -
Other names 3,3-bis(trifluoromethyl)-3-fluoro-propyne

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:24690-53-7 SDS

24690-53-7Upstream product

24690-53-7Downstream Products

24690-53-7Relevant academic research and scientific papers

Reaction of organylxenonium(II)salts, [RXe][Y], with organyl iodides, R'I, in anhydrous HF: Scope and limitation of a new synthetic approach to iodonium salts, [RR'I][Y]

Frohn, Hermann-Josef,Bardin, Vadim V.

experimental part, p. 2616 - 2620 (2012/05/31)

Perfluoroalkynylxenonium salts, [RXe][BF4] (R = CF 3C≡C, (CF3)22CFC≡C), reacted with organyl iodides, R'I (R' = 3-FC6H4, C6F 5, CF2 ≡CF, CF3CH2; no reaction with R' = CF3CF2CF2)in anhydrous HF to yield the corresponding asymmetric polyfluorinated iodonium salts, [RR'I][Y]. The action of the arylxenonium salt, [C6F5Xe]-[BF4], and the cycloalkenylxenonium salt, [cyclo-1,4-C6F7Xe]-[AsF6], on 4-FC6H4I gave [C6F5(4-FC 6H4)I][BF4] and [cyclo-1,4-C 6F7(4-FC6H4)I][AsF6], respectively, besides the symmetric iodonium salt, [(4-FC6H4)2 2I][Y]. But the aryl-, as well as the cycloalkenylxenonium salt, did not react with C6F5I, CF2 =CFI, and CF 3CH2I.

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