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68892-13-7

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68892-13-7 Usage

General Description

1-Phenyldecane-1,3-dione is a complex chemical compound that is classified under the category of Acetophenones. It is also known by its IUPAC name, 1-phenyldecane-1,3-dione. Its molecular formula is ?C17H24O2, has a molecular weight of 260.38, and a monoisotopic mass of 260.180. The chemical's structure carries two carbonyl groups at each end of a long decane chain, with a phenyl group attached to one end. It usually appears as a clear, colorless liquid and is widely utilized in the pharmaceutical industry and chemical research sectors due to its vital chemical properties. It is typically used as an organic intermediate compound during various types of chemical reactions. However, it is necessary to handle and store this chemical compound with care as it may pose certain health risks if not properly managed.

Check Digit Verification of cas no

The CAS Registry Mumber 68892-13-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,8,9 and 2 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 68892-13:
(7*6)+(6*8)+(5*8)+(4*9)+(3*2)+(2*1)+(1*3)=177
177 % 10 = 7
So 68892-13-7 is a valid CAS Registry Number.
InChI:InChI=1/C16H22O2/c1-2-3-4-5-9-12-15(17)13-16(18)14-10-7-6-8-11-14/h6-8,10-11H,2-5,9,12-13H2,1H3

68892-13-7SDS

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-phenyldecane-1,3-dione

1.2 Other means of identification

Product number -
Other names 1(phenyl)-1,3decanedione

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:68892-13-7 SDS

68892-13-7Downstream Products

68892-13-7Relevant articles and documents

Synthesis of Unnatural 2-Substituted Quinolones and 1,3-Diketones by a Member of Type III Polyketide Synthases from Huperzia serrata

Wang, Juan,Wang, Xiao-Hui,Liu, Xiao,Li, Jun,Shi, Xiao-Ping,Song, Yue-Lin,Zeng, Ke-Wu,Zhang, Le,Tu, Peng-Fei,Shi, She-Po

supporting information, p. 3550 - 3553 (2016/08/16)

A curcuminoids, benzalacetone-, and quinolone-producing type III polyketide synthase (HsPKS3) from Huperzia serrata uniquely catalyzes the formation of unnatural 2-substituted quinolones and 1,3-diketones via head-to-head condensation of two completely different substrates. The broad range of substrate tolerance of HsPKS3 facilitates accessing structurally diverse 2-substituted quinolones and 1,3-diketones.

Biosynthesis of 2-Alkyl-4(1H)-Quinolones in Pseudomonas aeruginosa: Potential for Therapeutic Interference with Pathogenicity

Pistorius, Dominik,Ullrich, Angelika,Lucas, Simon,Hartmann, Rolf W.,Kazmaier, Uli,Mueller, Rolf

body text, p. 850 - 853 (2012/02/04)

-

Process for base-promoted condensation reactions and base reagent therefor

-

, (2008/06/13)

A method for the preparation of 1,3-diketones is disclosed wherein the method comprises the steps of:(A) mixing an alkali metal base with a hindered alcohol in an aromatic hydrocarbon solvent;(B) boiling the mixture and azeotropically distilling water formed by the reaction between the base and the alcohol, whereby a solution of a hindered alkali metal alkoxide is formed in situ in the solvent;(C) mixing an ester with the solution of the hindered alkali metal alkoxide in the aromatic hydrocarbon solvent; and then(D) adding a ketone to the mixture.

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