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1,4-Hexanedione, 3,3,5-trimethyl-1-phenyl-, also known as 3,3,5-Trimethyl-1-phenylhexane-1,4-dione, is an organic compound with the chemical formula C15H22O2. It is a colorless liquid with a molecular weight of 234.33 g/mol. 1,4-Hexanedione, 3,3,5-trimethyl-1-phenyl- is characterized by its unique structure, featuring a hexanedione backbone with three methyl groups attached to the third carbon and a phenyl group connected to the first carbon. It is primarily used as a synthetic intermediate in the production of various chemicals, pharmaceuticals, and fragrances. Due to its reactive ketone groups, it can participate in various chemical reactions, such as condensation, reduction, and oxidation. However, it is important to handle 1,4-Hexanedione, 3,3,5-trimethyl-1-phenyl- with care, as it may have potential health hazards and should be stored away from heat and open flames.

66388-84-9

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66388-84-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66388-84-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,3,8 and 8 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 66388-84:
(7*6)+(6*6)+(5*3)+(4*8)+(3*8)+(2*8)+(1*4)=169
169 % 10 = 9
So 66388-84-9 is a valid CAS Registry Number.

66388-84-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3,5-Trimethyl-1-phenylhexan-1,4-dion

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

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More Details:66388-84-9 SDS

66388-84-9Relevant academic research and scientific papers

Oxovanadium-Induced Oxidative Desilylation for the Selective Synthesis of 1,4-Diketones

Fujii Takashi,Hirao, Toshikazu,Ohshiro, Yoshiki

, p. 5823 - 5826 (2007/10/02)

Silyl enol ethers underwent the VO(OR)Cl2-induced homo- or cross-coupling giving 1,4-diketones selectively via one-electron oxidative desilylation.

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