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1,5-Cyclohexadiene-1-carboxaldehyde, 4,4-dimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

97997-08-5

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97997-08-5 Usage

Physical state

Highly reactive and flammable liquid

Uses

a. Chemical intermediate in the synthesis of various organic compounds
b. Production of fragrances and flavors
c. Manufacturing of pharmaceuticals and other fine chemicals

Hazardous properties

a. Potential for causing irritation to the skin
b. Potential for causing irritation to the eyes
c. Potential for causing irritation to the respiratory system

Safety precautions

Handle with care due to its hazardous properties

Check Digit Verification of cas no

The CAS Registry Mumber 97997-08-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,9,9 and 7 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 97997-08:
(7*9)+(6*7)+(5*9)+(4*9)+(3*7)+(2*0)+(1*8)=215
215 % 10 = 5
So 97997-08-5 is a valid CAS Registry Number.

97997-08-5Relevant articles and documents

A General Method for the Preparation of γ-Substituted Cyclohexenals and Cycloheptenals

Jones, Tood K.,Denmark, Scott E.

, p. 4037 - 4045 (2007/10/02)

A general procedure for the preparation of γ-substituted or β'-unsaturated cycloalkenals is described.Starting from 2-cycloalkenones substituents may be introduced as nucleophiles by 1,4-addition followed by trapping of the regiospecifically generated enolate (86-92percent).Peracid oxidation of the enol silane derivative produces an α-hydroxy ketone which, after protection (70-93percent), is homologated to an enol ether by a Horner-Wittig reaction.Mild hydrolysis of the labile vinylogous acetal produces the aldehydes in good yields (62-75percent).Advantages of this method in comparison to known procedures are discussed as are other unsuccessful approaches to this substitution pattern.

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