34183-01-2 Usage
Description
Methanone, (2,4-dichlorophenyl)(4-hydroxyphenyl)-, also known as 2,4-dichloro-4''-hydroxybenzophenone, is an organic compound with a molecular structure that features a carbonyl group (C=O) bonded to a 2,4-dichlorophenyl group and a 4-hydroxyphenyl group. Methanone, (2,4-dichlorophenyl)(4-hydroxyphenyl)is characterized by its chemical properties and potential applications in various industries.
Uses
Used in Agricultural Industry:
Methanone, (2,4-dichlorophenyl)(4-hydroxyphenyl)is used as a key intermediate compound in the synthesis of herbicides for controlling specific weeds in rice fields. Specifically, it is utilized in the production of a herbicide compound that targets Echinochloa crus-galli, Scirpus hotarui, and Monochoria vaginalis. The application of this compound in herbicides helps improve the efficiency of weed control, leading to better crop yield and reduced competition for resources between the rice plants and the targeted weeds.
Preparation
Preparation by reaction of 2,4-dichlorobenzoyl chloride with phenol in the presence of aluminium chloride.
Check Digit Verification of cas no
The CAS Registry Mumber 34183-01-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,1,8 and 3 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 34183-01:
(7*3)+(6*4)+(5*1)+(4*8)+(3*3)+(2*0)+(1*1)=92
92 % 10 = 2
So 34183-01-2 is a valid CAS Registry Number.
34183-01-2Relevant articles and documents
Synthesis and structure-activity relationships of benzophenone hydrazone derivatives with insecticidal activity
Boeger, Manfred,Duerr, Dieter,Gsell, Laurenz,Hall, Roger G.,Karrer, Friedrich,Kristiansen, Odd,Maienfisch, Peter,Pascual, Alfons,Rindlisbacher, Alfred
, p. 191 - 202 (2007/10/03)
A broad range of benzophenone hydrazone derivatives was prepared and tested against selected chewing insect pests, allowing the analysis of structure-activity relationships. Good activity was found only when the aromatic rings were substituted at the 4-positions with an halogen atom and a triflate or perhaloalkoxy group. In contrast, a number of substituents on the hydrazone part led to active compounds, the best results being achieved with acyl-type substituents. The excellent laboratory and greenhouse activity of the best representatives was confirmed in semi-field trials against Spodoptera littoralis. ° 2001 Society of Chemical Industry.