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l-Cyclohexy1-4,4,4-trifluoro- 3-(trifluoroMethyl)butane-l,3-diol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

923018-85-3

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923018-85-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 923018-85-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,3,0,1 and 8 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 923018-85:
(8*9)+(7*2)+(6*3)+(5*0)+(4*1)+(3*8)+(2*8)+(1*5)=153
153 % 10 = 3
So 923018-85-3 is a valid CAS Registry Number.
InChI:InChI=1S/C11H16F6O2/c12-10(13,14)9(19,11(15,16)17)6-8(18)7-4-2-1-3-5-7/h7-8,18-19H,1-6H2

923018-85-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-Butanediol, 1-cyclohexyl-4,4,4-trifluoro-3-(trifluoromethyl)-

1.2 Other means of identification

Product number -
Other names -

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:923018-85-3 SDS

923018-85-3Downstream Products

923018-85-3Relevant academic research and scientific papers

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).

Process for producing fluorine-containing diol and its derivatives

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Page/Page column 6, (2008/06/13)

A process for producing a fluorine-containing diol represented by the formula [2], includes reducing a hydroxy ketone represented by the formula [1], by hydrogen in the presence of a ruthenium catalyst. The ruthenium catalyst may be a solid-phase catalyst

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