6781-42-6 Usage
Description
1,3-Diacetylbenzene, also known as δ-diketone, is an organic compound that has been found to induce neuropathological changes in the rodent central and peripheral nervous systems. It is characterized by its unique chemical structure, which makes it a valuable compound in various applications.
Uses
1. Used in Organic Synthesis:
1,3-Diacetylbenzene is used as an important raw material and intermediate for the preparation of polyhydroxylated analogs in the field of organic synthesis. Its unique chemical properties allow it to serve as a key component in the creation of various complex organic molecules.
2. Used in Pharmaceutical Industry:
1,3-Diacetylbenzene is used as a starting material for the synthesis of various pharmaceutical compounds. Its ability to induce neuropathological changes in rodents makes it a potential candidate for the development of drugs targeting the central and peripheral nervous systems.
3. Used in Chemical Research:
1,3-Diacetylbenzene is utilized as a research compound in the field of chemistry, particularly in the study of δ-diketone chemistry and its applications. Its unique properties and reactivity make it an interesting subject for further investigation and potential discovery of new chemical reactions and processes.
4. Used in Material Science:
1,3-Diacetylbenzene may also find applications in the development of new materials, such as polymers and composites, due to its chemical structure and properties. Its potential use in material science could lead to the creation of novel materials with specific properties tailored for various industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 6781-42-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,8 and 1 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6781-42:
(6*6)+(5*7)+(4*8)+(3*1)+(2*4)+(1*2)=116
116 % 10 = 6
So 6781-42-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H10O2/c1-7(11)9-4-3-5-10(6-9)8(2)12/h3-6H,1-2H3
6781-42-6Relevant articles and documents
Preparation method 1,3 - diacyl benzene
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Paragraph 0046; 0048; 0055-0058; 0062-0075, (2021/08/25)
The preparation method of 1-3 - diacyl benzene comprises the following steps: reacting m-phthalic aldehyde with an alkyl magnesium halide to form an intermediate as shown II. The intermediate shown in Formula II is subjected to an oxidation reaction under the action of an oxidant to generate III, 1 diacyl benzene as shown 3 . In-flight R1 . R2 Alkyl groups from the alkyl magnesium halides, respectively. The method has the advantages of simple process, safety, environmental protection, high target product yield, high purity and the like, and can realize large-scale industrial production.
Photoinduced Acetylation of Anilines under Aqueous and Catalyst-Free Conditions
Yang, Yu-Ming,Yan, Wei,Hu, Han-Wei,Luo, Yimin,Tang, Zhen-Yu,Luo, Zhuangzhu
, p. 12344 - 12353 (2021/09/02)
A green and efficient visible-light induced functionalization of anilines under mild conditions has been reported. Utilizing nontoxic, cost-effective, and water-soluble diacetyl as photosensitizer and acetylating reagent, and water as the solvent, a variety of anilines were converted into the corresponding aryl ketones, iodides, and bromides. With advantages of environmentally friendly conditions, simple operation, broad substrate scope, and functional group tolerance, this reaction represents a valuable method in organic synthesis.
Method for removing acyl group in diazo of aryl diazonium salt
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Paragraph 0052; 0074-0076; 0088, (2019/02/13)
The invention provides a method for removing an acyl group in diazo of an aryl diazonium salt. The method is characterized in that the aryl diazonium salt and its derivative and an ortho-dicarbonyl compound undergo an illumination reaction to obtain a corresponding arylacyl product. The method has the advantages of high yield of the product, no metal involvement, and simple process.