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1,1,1-trifluorodecane-2,4-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

332-82-1

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332-82-1 Usage

Family

Alpha-diketones

Functional groups

Two carbonyl groups

Usage

a. Precursor in the synthesis of pharmaceuticals and agrochemicals
b. Building block in the production of dyes and pigments

Reactivity

High level of reactivity

Chemical transformations

Known to undergo various chemical transformations

Importance

Versatile and important compound in the field of organic chemistry

Check Digit Verification of cas no

The CAS Registry Mumber 332-82-1 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 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 332-82:
(5*3)+(4*3)+(3*2)+(2*8)+(1*2)=51
51 % 10 = 1
So 332-82-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H15F3O2/c1-2-3-4-5-6-8(14)7-9(15)10(11,12)13/h2-7H2,1H3

332-82-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,1-trifluorodecane-2,4-dione

1.2 Other means of identification

Product number -
Other names 1,1,1-Trifluor-decan-2,4-dion

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:332-82-1 SDS

332-82-1Downstream Products

332-82-1Relevant academic research and scientific papers

Keto-enol and enol-enol tautomerism in trifluoromethyl-β-diketones

Sloop, Joseph C.,Bumgardner, Carl L.,Washington, Gary,Loehle, W. David,Sankar, Sabapathy S.,Lewis, Adam B.

, p. 780 - 786 (2008/03/27)

The keto-enol (K?E) and enol-enol (E?E) equilibria of a variety of trifluoromethyl-β-diketones were investigated using 1H, 13C, 19F NMR spectroscopy, infrared spectroscopy and ultraviolet-visible spectrophotometry in nonpolar solvents. In general, NMR, IR and UV spectral evidence indicates that trifluoromethyl-β-diketones exist as mixtures of two chelated cis-enol forms in nonpolar media. Infrared spectroscopy and ultraviolet spectrophotometry show the E?E equilibrium lies in the direction of the enol form which maximizes conjugation in most cases. Exceptions are noted and discussed.

Synthesis of fluorinated heterocycles

Sloop, Joseph C.,Bumgardner, Carl L.,Loehle, W. David

, p. 135 - 147 (2007/10/03)

Selected 1,3-diketones having a trifluoromethyl group and/or a fluorine in the 2-position were condensed with aromatic hydrazines, hydroxylamine, urea, thiourea, guanidine, and substituted anilines producing pyrazoles, isoxazoles, pyrimidines, and quinolines, respectively, in yields ranging from 27 to 87%.

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