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10487-11-3

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10487-11-3 Usage

General Description

1,1,1,7,7,7-HEXAFLUORO-2,6-DIHYDROXY-2,6-BIS(TRIFLUOROMETHYLHEPTAN-4-ONE) is a chemical compound with a complex molecular structure. It contains six fluorine atoms and two hydroxyl groups, as well as a trifluoromethyl group and a heptan-4-one moiety. This chemical is used as a building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. It is also employed as a reagent in organic synthesis and as a solvent in various industries. The compound is known for its high stability and low reactivity, as well as its ability to modify the properties of other molecules in complex chemical reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 10487-11-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,8 and 7 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 10487-11:
(7*1)+(6*0)+(5*4)+(4*8)+(3*7)+(2*1)+(1*1)=83
83 % 10 = 3
So 10487-11-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H6F12O3/c10-6(11,12)4(23,7(13,14)15)1-3(22)2-5(24,8(16,17)18)9(19,20)21/h23-24H,1-2H2

10487-11-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,1,7,7,7-hexafluoro-2,6-dihydroxy-2,6-bis(trifluoromethyl)heptan-4-one

1.2 Other means of identification

Product number -
Other names 1,1,1,7,7,7-Hexafluor-2,6-bis(trifluormethyl)-2,6-dihydroxyheptan-4-on

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:10487-11-3 SDS

10487-11-3Relevant articles and documents

The cross-aldol reaction of hexafluoroacetone (HFA) with ketones catalyzed by an acid

Komata, Takeo,Matsunaga, Kei,Hirotsu, Yoshiki,Akiba, Shinya,Ogura, Katsuyuki

, p. 902 - 909 (2008/03/14)

The cross-aldol reactions of hexafluoroacetone (HFA) and ketones using an acid catalyst are reported. When concentrated sulfuric acid was employed as the catalyst, HFA reacted regioselectively with various ketones at 50-100 °C to give the aldol adducts (6) in good yields. The reaction is initiated by an acid-catalyzed transformation of the ketone into the corresponding enol that reacts with HFA. The obtained adducts (6) can be reduced with hydrogen under a Ru/C catalyst to lead to the corresponding fluorine-containing diols (13).

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