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Decanoyl fluoride, also known as decanoyl trifluoromethyl ether or decanoyl fluoride, is a chemical compound with the molecular formula C10H19FO. It is a colorless liquid with a density of 0.87 g/cm3 and a boiling point of 200°C. Decanoyl fluoride is an acylating agent, which means it can transfer an acyl group (in this case, the decanoyl group) to another molecule, often in the presence of a catalyst. Decanoyl fluoride is used in organic synthesis, particularly in the preparation of esters, amides, and other derivatives of carboxylic acids. It is also employed in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals due to its reactivity and stability.

334-47-4

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334-47-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 334-47-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,3 and 4 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 334-47:
(5*3)+(4*3)+(3*4)+(2*4)+(1*7)=54
54 % 10 = 4
So 334-47-4 is a valid CAS Registry Number.

334-47-4SDS

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 decanoyl fluoride

1.2 Other means of identification

Product number -
Other names Decanoylfluoride

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:334-47-4 SDS

334-47-4Relevant academic research and scientific papers

Rhodium-catalyzed interconversion between acid fluorides and thioesters controlled using heteroatom acceptors

Arisawa, Mieko,Yamada, Toru,Yamaguchi, Masahiko

supporting information; experimental part, p. 6090 - 6092 (2011/01/04)

A rhodium complex catalyzed the equilibrium acyl transfer reaction between acid fluorides and thioesters. In the presence of fluoride or thiolate acceptors, the reaction could be shifted to either product. RhH(PPh 3)4-dppe catalyzed the reaction of acid fluorides and diorgano disulfides in the presence of triphenylphosphine giving thioesters, which was accompanied by triphenylphosphine difluoride. The same complex catalyzed the reaction of aryl thioesters and hexafluorobenzene giving acid fluorides, which was accompanied by 1,4-di(arylthio)-2,3,5,6- tetrafluorobenzenes.

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