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4-(2-hydroxy-3,5-dimethyl-phenyl)-4-oxo-butanoic acid is a complex organic compound with the molecular formula C12H14O4. It is characterized by a 4-oxobutanoic acid backbone, which is a four-carbon chain with a carbonyl group at the fourth position. The phenyl ring attached to this backbone is substituted with a hydroxyl group at the 2-position and two methyl groups at the 3 and 5 positions, respectively. This chemical structure gives the compound unique properties and potential applications in various fields, such as pharmaceuticals or chemical research. The compound's specific arrangement of functional groups and substituents may influence its reactivity, solubility, and other physical and chemical characteristics, making it a subject of interest for further study and development.

7356-03-8

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7356-03-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7356-03-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,5 and 6 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7356-03:
(6*7)+(5*3)+(4*5)+(3*6)+(2*0)+(1*3)=98
98 % 10 = 8
So 7356-03-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H14O4/c1-7-5-8(2)12(16)9(6-7)10(13)3-4-11(14)15/h5-6,16H,3-4H2,1-2H3,(H,14,15)

7356-03-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(2-hydroxy-3,5-dimethylphenyl)-4-oxobutanoic acid

1.2 Other means of identification

Product number -
Other names 4-(2-Hydroxy-3,5-dimethyl-phenyl)-4-oxo-buttersaeure

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 -
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More Details:7356-03-8 SDS

7356-03-8Relevant academic research and scientific papers

Photochemical Versus Aluminium Chloride-Catalyzed Fries Rearrangement of Aryl Hydrogen Succinates. Synthesis of 2(3H)-Furanones

Fillol, Luis,Martinez-Utrilla, Roberto,Miranda, Miguel A.,Morera, Isabel M.

, p. 863 - 870 (2007/10/02)

The photochemical and aluminium chloride-catalyzed Fries rearrangement of a series of aryl hydrogen succinates 3 a-f to the corresponding 4-oxoacids 1 a-f are compared.Both approaches are complementary: the photochemical process is more general and becomes the method of choice for the succinoylation of phenols supporting alkoxy or hydroxy substituents, while the classical rearrangement is superior in the presence of alkyl or halogen substituents.These results are applied to the preparation of the 2(3H)-furanones 2 a-f. - Keywords: Fries rearrangement; Photo-Fries rearrangement; Aryl hydrogen succinates; 4-Oxoacids; 2(3H)-Furanones.

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