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2525-85-1

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2525-85-1 Usage

Class

Organic compound

Subclass

Ketones

Derivative

Fluorinated derivative of 1,4-diphenyl-1,4-diketone

Building block

Used for the synthesis of various organic compounds

Chemical structure

Two phenyl groups attached to a butane-1,3-dione skeleton with four fluorine atoms attached to the butane moiety

Potential applications

Pharmaceuticals, agrochemicals, and materials science

Unique properties

Chemical reactivity due to the presence of fluorine atoms and the dione structure

Check Digit Verification of cas no

The CAS Registry Mumber 2525-85-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,2 and 5 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2525-85:
(6*2)+(5*5)+(4*2)+(3*5)+(2*8)+(1*5)=81
81 % 10 = 1
So 2525-85-1 is a valid CAS Registry Number.

2525-85-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,3,3-tetrafluoro-1,4-diphenylbutane-1,4-dione

1.2 Other means of identification

Product number -
Other names 2,2,3,3-TETRAFLUORO-1,4-DIPHENYL-BUTANE-1,4-DIONE

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:2525-85-1 SDS

2525-85-1Downstream Products

2525-85-1Relevant articles and documents

New entry for fluorinated carbocycles: Unprecedented 3,6-disubstituted 1,1,2,2-tetrafluorocyclohexane derivatives

Yamada, Shigeyuki,Hashishita, Shohei,Konishi, Hideaki,Nishi, Yuji,Kubota, Toshio,Asai, Tomoyuki,Ishihara, Takashi,Konno, Tsutomu

, p. 47 - 58 (2017/06/14)

The synthetic protocols for symmetrical/unsymmetrical 3,6-disubstituted 1,1,2,2-tetrafluorocyclohexane molecules were successfully established for the first time. Some of thus obtained tetrafluorinated cyclohexanes underwent recrystallization to afford trans-configured products preferentially. One of the unsymmetrical trans-disubstituted tetrafluorocyclohexanes, trans-1-ethyl-2,2,3,3-tetrafluoro-4-[4-(trans-4-n-propylcyclohex-1-yl)phenyl]cyclohexane, was found to possess a low birefringence Δn (0.073) and a large negative dielectric anisotropy Δε (–9.4) in a binary mixture system, which were very prominent as characteristics of LC molecules in VA-mode driving LC displays.

Oxidative cross-coupling of ββ-difluoroenol silyl ethers with nucleophiles: A dipole-inversion method to difluoroketones

Uneyama, Kenji,Tanaka, Hiroaki,Kobayashi, Satoru,Shioyama, Manabu,Amii, Hideki

, p. 2733 - 2736 (2007/10/03)

Oxidative cross-coupling of α-aryl-β,β-difluoroenol silyl ethers with heteroaromatics in the presence of Cu(OTf)2 in wet acetonitrile proceeds smoothly, affording heteroaryldifluoromethyl aryl ketones in 61-88% yields. Alcohols also react as nu

REDUCTION OF POLYFLUORINATED CARBONYL COMPOUNDS BY ETHOXYMAGNESIUM BROMIDE

Dormidontov, Yu. P.,Shadrina, L. P.

, p. 241 - 244 (2007/10/02)

The reduction of perfluoroalkyl phenyl ketones and diketones with ethoxymagnesium bromide takes place readily in the absence of branching at the α-carbon atom of the aliphatic radical and in the absence of a substituent or in the presence of only one orth

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