35112-27-7 Usage
Uses
Used in Insecticide Production:
Ethyl 2,5-dichlorobenzoate is used as an active ingredient in insecticides for its ability to effectively control and eliminate pests. Its chemical properties make it a suitable compound for formulating insecticidal products that protect crops and other areas from insect infestations.
Used in Perfumery:
In the perfume industry, Ethyl 2,5-dichlorobenzoate is used as a fragrance ingredient for its strong, sweet odor. It contributes to the overall scent profile of various perfumes and colognes, enhancing their appeal and longevity.
Used in Pharmaceutical Manufacturing:
Ethyl 2,5-dichlorobenzoate serves as an intermediate in the production of pharmaceuticals, aiding in the synthesis of various drugs and medications. Its chemical properties make it a valuable component in the development of new and improved pharmaceutical compounds.
Used in Chemical Synthesis:
As an intermediate in chemical synthesis, Ethyl 2,5-dichlorobenzoate is used for the production of other chemicals, including dyes, plastics, and resins. Its versatility in chemical reactions allows for the creation of a wide range of products across various industries.
Environmental Applications:
Ethyl 2,5-dichlorobenzoate is known for its low toxicity to aquatic organisms, making it a suitable compound for use in certain environmental applications where minimal ecological impact is desired. Its properties can be harnessed to develop products that are both effective and environmentally friendly.
Check Digit Verification of cas no
The CAS Registry Mumber 35112-27-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,1,1 and 2 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 35112-27:
(7*3)+(6*5)+(5*1)+(4*1)+(3*2)+(2*2)+(1*7)=77
77 % 10 = 7
So 35112-27-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H8Cl2O2/c1-2-13-9(12)7-5-6(10)3-4-8(7)11/h3-5H,2H2,1H3
35112-27-7Relevant academic research and scientific papers
Directed magnesiation of polyhaloaromatics using the tetramethylpiperidylmagnesium reagents TMP2Mg×2 LiCl and TMPMgCl×LiCl
Unsinn, Andreas,Rohbogner, Christoph J.,Knochel, Paul
supporting information, p. 1553 - 1560 (2013/06/27)
A convenient and efficient functionalization of polyhaloaromatics via regioselective magnesiation has been developed. Starting from simple, inexpensive but structurally challenging arenes, metallation by magnesium amide bases was achieved under mild conditions. The desired Grignard reagents were stable towards aryne formation, were obtained in good yields within short reaction times and could be reacted with a variety of typical electrophiles, providing attractive, functionalized building blocks in good to excellent yields. As an application we have prepared the antimicrobial natural product 2,6-dichloro-3-phenethylphenol isolated from the New Zealand liverwort Riccardia marginata. This synthesis involves a mixed bimetallic compound prepared via metallation of a phenylboronic acid pinacol ester derivative and subsequent selective cross-coupling. Copyright
Regio- and chemoselective C-H chlorination/bromination of electron-deficient arenes by weak coordination and study of relative directing-group abilities
Sun, Xiuyun,Shan, Gang,Sun, Yonghui,Rao, Yu
supporting information, p. 4440 - 4444 (2013/05/22)
It's all relative: A practical and efficient PdII-catalyzed regio- and chemoselective chlorination/bromination has been developed for the facile synthesis of a broad range of aromatic chlorides. The reaction demonstrates excellent reactivity, good functional-group tolerance, and high yields. A preliminary study was conducted to evaluate relative directing-group abilities of various functionalities. Copyright
