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Diacetic acid 5-methyl-6-oxo-2,4-cyclohexadien-1-ylidene ester, also known as 5-methyl-6-oxo-2,4-cyclohexadien-1-ylidene diacetate, is a chemical compound with the molecular formula C10H10O5. It is a derivative of diacetic acid, featuring a cyclohexadienyl ring with a methyl group at the 5-position and a carbonyl group at the 6-position. Diacetic acid 5-methyl-6-oxo-2,4-cyclohexadien-1-ylidene ester is characterized by its conjugated diene system and the presence of two acetate ester groups. It is an organic compound that can be used in the synthesis of various chemical products, particularly in the field of organic synthesis and pharmaceuticals. Due to its reactivity and structural features, it may have potential applications in the development of new drugs or as an intermediate in the production of other complex molecules.

7218-17-9

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7218-17-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7218-17-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,1 and 8 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7218-17:
(6*7)+(5*2)+(4*1)+(3*8)+(2*1)+(1*7)=89
89 % 10 = 9
So 7218-17-9 is a valid CAS Registry Number.

7218-17-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6,6-diacetoxy-2-methyl-2,4-cyclohexadienone

1.2 Other means of identification

Product number -
Other names 5-methyl-6-oxocyclohexa-2,4-diene-1,1-diyl diacetate

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:7218-17-9 SDS

7218-17-9Relevant academic research and scientific papers

Experimental and computational studies on the [3,3]- and [3,5]-sigmatropic rearrangements of acetoxycyclohexadienones: A non-ionic mechanism for acyl migration

Sharma, Shikha,Rajale, Trideep,Cordes, David B.,Hung-Low, Fernando,Birney, David M.

supporting information, p. 14438 - 14447 (2013/10/21)

Flash vacuum pyrolysis studies of substituted 6-acetoxy-2,4- cyclohexadienones (3 and 10) from 300 to 500 C provide strong experimental evidence that direct [3,5]-sigmatropic rearrangements in these molecules are favored over the more familiar [3,3]-sigma

A solvolytic C-C cleavage reaction of 6-acetoxycyclohexa-2,4-dienones: Mechanistic implications for the intradiol catechol dioxygenases

Eley,Crowley,Bugg

, p. 2091 - 2097 (2007/10/03)

6-Acetoxycyclohexa-2,4-dienones are found to undergo a rapid reaction in methanol/water under mildly basic conditions to give an acyclic ketoester as the major product for 6-phenyl and 6-methyl substrates. Reaction monitoring by UV spectroscopy indicates

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