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374-41-4

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374-41-4 Usage

General Description

3,3,4,4,4-Pentafluorobutan-2-one is a chemical compound with the molecular formula C4F8O. It is a colorless liquid that is highly volatile and flammable. The compound is commonly used as a solvent and as a precursor for the production of other fluorinated compounds. It is also used in the synthesis of pharmaceuticals and agrochemicals. The compound has a wide range of industrial applications, including in the manufacture of plastics, polymers, and electronics. Due to its high reactivity and potential environmental and health hazards, 3,3,4,4,4-Pentafluorobutan-2-one should be handled with care and in accordance with appropriate safety measures and regulations.

Check Digit Verification of cas no

The CAS Registry Mumber 374-41-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,7 and 4 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 374-41:
(5*3)+(4*7)+(3*4)+(2*4)+(1*1)=64
64 % 10 = 4
So 374-41-4 is a valid CAS Registry Number.
InChI:InChI=1/C4H3F5O/c1-2(10)3(5,6)4(7,8)9/h1H3

374-41-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3,4,4,4-Pentafluorobutan-2-one

1.2 Other means of identification

Product number -
Other names 3,3,4,4,4-PENTAFLUOROBUTAN-2-ONE

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:374-41-4 SDS

374-41-4Relevant articles and documents

(Z) -Trifluoromethyl-Trisubstituted Alkenes or Isoxazolines: Divergent Pathways from the Same Allene

Liu, Chaolun,Rowland, Casey A.,Tius, Marcus A.,Yap, Glenn P. A.

supporting information, p. 7208 - 7212 (2020/10/02)

Because of a charge-dipole interaction involving nonbonding electron pairs on fluorine, protonation of trifluoromethyl allenes leads to tri- or tetrasubstituted alkenes with high (Z)-selectivity. Treatment of the same allenes with catalytic Au(I) initiates a reaction cascade that produces isoxazolines in high yield.

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