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3-(2,3,4-Trimethylbenzoyl)propionsaeure, also known as 3-(2,3,4-trimethylbenzoyl)propionic acid, is a chemical compound with the molecular formula C13H16O4. It is a derivative of propionic acid, featuring a 2,3,4-trimethylbenzoyl group attached to the third carbon of the propionic acid backbone. 3-(2,3,4-Trimethylbenzoyl)propionsaeure is characterized by its aromatic ring structure, with three methyl groups (CH3) attached to the benzene ring, which influences its chemical properties and reactivity. It is often used in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds due to its unique structure and functional groups. The compound's properties, such as its solubility and stability, can be influenced by the presence of the trimethylbenzoyl group, making it a valuable building block in organic synthesis.

1082-77-5

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1082-77-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1082-77-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,8 and 2 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1082-77:
(6*1)+(5*0)+(4*8)+(3*2)+(2*7)+(1*7)=65
65 % 10 = 5
So 1082-77-5 is a valid CAS Registry Number.

1082-77-5Downstream Products

1082-77-5Relevant academic research and scientific papers

SCHWEFELVERBINDUNGEN DES ERDOELS XV. METHYL-5,6,7,8-TETRAHYDRODINAPHTHOTHIOPHENE UND METHYLDINAPHTHOTHIOPHENE

Boberg, Friedrich,Jachiewicz, Adam,Garming, Alfons

, p. 1 - 12 (2007/10/02)

A one pot synthesis gives methyl-5,6,7,8-tetrahydrodinaphthothiophenes (7) from methyl-1,2,3,4-tetrahydronaphthalen-1-ones (1) by bromination and sulfurization.Tetrahydro compounds 7 have been dehydrogenated to corresponding dinaphthothiophenes 8.Proofs for the constitutions are nmr data of 7, 8 and the independent synthesis of one compound 8.A reaction mechanism with 1,4-dithiine intermediates is discussed. Key words: Alkyl-1,2,3,4-tetrahydronaphthalen-1-ones; alkyl-5,6,7,8-tetrahydrodinaphthothiophenes; alkyldinaphthothiophenes; dehydrogenation with o-chlorobenzoquinone.

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