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2,5-Cyclohexadien-1-one, 4-butyl-4-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

66270-58-4

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66270-58-4 Usage

Structure

It is a cyclic enone, containing a double bond and a carbonyl group within a ring structure.

Uses

Flavoring Agent: Commonly used in the food and beverage industry for flavor enhancement.
Perfumes: Utilized in the production of perfumes and aromatic products due to its pleasant scent.
Pharmaceuticals: Potential applications in pharmaceuticals for drug development.

Caution

Handling this chemical requires caution due to potential hazardous properties.

Check Digit Verification of cas no

The CAS Registry Mumber 66270-58-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,2,7 and 0 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 66270-58:
(7*6)+(6*6)+(5*2)+(4*7)+(3*0)+(2*5)+(1*8)=134
134 % 10 = 4
So 66270-58-4 is a valid CAS Registry Number.

66270-58-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-butyl-4-methylcyclohexa-2,5-dien-1-one

1.2 Other means of identification

Product number -
Other names 4-methyl-4-n-butyl-cyclohexadiene-2,5-one-1

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:66270-58-4 SDS

66270-58-4Relevant academic research and scientific papers

On the mechanism of the dimethyldioxirane oxidation of σ(H) adducts (Meisenheimer complexes) generated from nitroarenes and carbanions

Adam, Waldemar,Makosza, Mieczyslaw,Zhao, Cong-Gui,Surowiec, Marek

, p. 1099 - 1101 (2000)

The mechanism of the novel dimethyldioxirane (DMD) oxidation of σ(H) adducts (Meisenheimer complexes) generated from nitroarenes and carbanions was elucidated. The proposed mechanism, which is akin to that of the oxidative Nef reaction, is supported by the isolation of the cyclohexadienone intermediate and the lack of a primary kinetic isotopic effect. Protic solvents (H2O, MeOH) enhance the reactivity of DMD through intermolecular hydrogen bonding.

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