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56309-94-5

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56309-94-5 Usage

Description

Ketoketal, a white solid, is a versatile chemical compound that serves as an intermediate in various industries due to its unique chemical properties. It is known for its ability to be synthesized into a range of products, making it a valuable component in the development of pharmaceuticals and liquid crystals.

Uses

Used in Pharmaceutical Industry:
Ketoketal is used as a pharmaceutical intermediate for its ability to be transformed into various medicinal compounds. Its chemical structure allows for the creation of drugs that can target specific health conditions, making it an essential component in the development of new pharmaceuticals.
Used in Liquid Crystal Industry:
In the liquid crystal industry, Ketoketal is utilized as an intermediate for the production of liquid crystals. These liquid crystals are widely used in display technologies, such as televisions, computer monitors, and smartphones, due to their unique optical properties. The versatility of Ketoketal in this application contributes to the advancement of display technology and the development of high-quality screens.

Flammability and Explosibility

Notclassified

Check Digit Verification of cas no

The CAS Registry Mumber 56309-94-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,3,0 and 9 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 56309-94:
(7*5)+(6*6)+(5*3)+(4*0)+(3*9)+(2*9)+(1*4)=135
135 % 10 = 5
So 56309-94-5 is a valid CAS Registry Number.

56309-94-5 Well-known Company Product Price

  • Brand
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  • Packaging
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  • Alfa Aesar

  • (H55069)  Ketoketal, 97%   

  • 56309-94-5

  • 5g

  • 261.0CNY

  • Detail
  • Alfa Aesar

  • (H55069)  Ketoketal, 97%   

  • 56309-94-5

  • 25g

  • 972.0CNY

  • Detail

56309-94-5SDS

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 8-(4-Oxocyclohexyl)-1,4-Dioxaspiro[4.5]Decane

1.2 Other means of identification

Product number -
Other names 4-(1,4-dioxaspiro[4.5]decan-8-yl)cyclohexan-1-one

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:56309-94-5 SDS

56309-94-5Relevant articles and documents

SALT, ACID GENERATOR, RESIST COMPOSITION, AND METHOD FOR PRODUCING RESIST PATTERN

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Paragraph 0220, (2020/09/01)

PROBLEM TO BE SOLVED: To provide a salt capable of producing a resist pattern with a good mask error factor (MEF), and a resist composition containing the salt. SOLUTION: The salt represented by formula (I), an acid generator, and the resist composition containing the same are provided. [In the formula, Q1 and Q2 each represent a fluorine atom, a perfluoroalkyl group or the like; R1 and R2 each represent a hydrogen atom, a fluorine atom, a perfluoroalkyl group or the like; z represents an integer of 0-6; X1 represents *-CO-O-, *-O-CO-, *-O-CO-O- or *-O-; L1 represents a single bond or a saturated hydrocarbon group; A1 represents an optionally substituted divalent alicyclic hydrocarbon group; Ra represents an optionally substituted alicyclic hydrocarbon group, and -CH2- contained in the group may be substituted with -O-, -S-, -SO2- or -CO-, provided that at least one -CH2- contained in the alicyclic hydrocarbon group is substituted with -O- or -CO-; and Z+ represents an organic cation.] SELECTED DRAWING: None COPYRIGHT: (C)2020,JPOandINPIT

METHOD FOR PRODUCING 4,4'-BICYCLOHEXANEDIONE MONOKETAL

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Page/Page column 9-11, (2010/11/24)

Disclosed is a method for producing a 4,4'-bicyclohexanedione monoketal represented by the general formula (2) with high yield by a simple operation. In this method, 4,4'-bicyclohexanedione and a diol are reacted in the liquid phase in the presence of an acid catalyst while precipitating a 4,4'-bicyclohexanedione monoketal produced thereby.

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