23287-26-5 Usage
Description
METHYL 2-HYDROXY-3-METHYLBENZOATE, also known as Methyl 3-methylsalicylate, is an organic compound that serves as a crucial intermediate in various chemical syntheses. It is characterized by its unique chemical structure, which contributes to its diverse applications across different industries.
Uses
Used in Organic Synthesis:
METHYL 2-HYDROXY-3-METHYLBENZOATE is used as an important organic intermediate for the synthesis of various chemicals. Its versatile chemical structure allows it to be a key component in the production of a wide range of compounds.
Used in Pharmaceutical Industry:
METHYL 2-HYDROXY-3-METHYLBENZOATE is used as a vital raw material in the pharmaceutical sector. Its unique properties make it suitable for the development of new drugs and the improvement of existing ones.
Used in Agrochemicals:
In the agrochemical industry, METHYL 2-HYDROXY-3-METHYLBENZOATE is utilized as a key intermediate for the development of various agrochemical products, such as pesticides and fertilizers.
Used in Dyestuff Industry:
METHYL 2-HYDROXY-3-METHYLBENZOATE is employed in the dyestuff industry as a crucial raw material for the production of different types of dyes.
Used in Chemical Production:
METHYL 2-HYDROXY-3-METHYLBENZOATE is used to produce other chemicals, such as 2-(2-Hydroxy-3-methyl-phenyl)-propan-2-ol. The reaction occurs with the reagent Tetrahydrofuran, showcasing its versatility in chemical reactions and its importance in the synthesis of various compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 23287-26-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,2,8 and 7 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 23287-26:
(7*2)+(6*3)+(5*2)+(4*8)+(3*7)+(2*2)+(1*6)=105
105 % 10 = 5
So 23287-26-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H10O3/c1-6-4-3-5-7(8(6)10)9(11)12-2/h3-5,10H,1-2H3
23287-26-5Relevant articles and documents
Pd(OAc)2-catalyzed orthogonal synthesis of 2-hydroxybenzoates and substituted cyclohexanones from acyclic unsaturated 1,3-carbonyl compounds
Miyagi, Toshinori,Okada, Sho,Tada, Naoya,Sugihara, Masahiro,Kagawa, Natsuko,Takabatake, Tetsuhiko,Toyota, Masahiro
supporting information, p. 1653 - 1657 (2019/05/29)
A Pd-catalyzed orthogonal synthesis of substituted 2-hydroxybenzoates and substituted cyclohexanones was developed for the first time. The substituted 2-hydroxybenzoates were obtained from acyclic unsaturated 1,3-carbonyl compounds using a combination of catalytic Pd(OAc)2 and Cu(OAc)2. On the other hand, the substituted cyclohexanones were produced from similar substrates via catalytic Pd(OAc)2 and hydrogen chloride. Each transformation was clean, easy to work up, provided the desired compounds in good purities, and did not require column chromatography purification.
Microwave-Assisted Synthesis of Benzofuran-3(2H)-ones
Hu, Xiaojing,Lai, Huimin,Zhao, Fangfei,Hu, Shuyu,Sun, Qianqian,Fang, Lizhen
, p. 745 - 750 (2019/10/14)
A new method for the synthesis of benzofuran-3(2H)-ones under microwave conditions was developed. The reaction conditions were screened, and the scope of benzoate substrates was investigated. The results showed that our method could provide rapid access to these important dihydrobenzofuranones in 43% to 58% yields.
Gold promoted arylative cyclization of alkynoic acids with arenediazonium salts
Carrillo-Arcos, Ulises A.,Porcel, Susana
supporting information, p. 1837 - 1842 (2018/03/23)
Alkynoic acids derived from salicylic acid and analogues undergo arylative cyclization with arenediazonium salts promoted by gold in the absence of external ligands. The reaction is thermally induced and proceeds even in the absence of light. A difference in regioselectivity has been found compared with that observed in the cycloisomerization process of the same type of compounds.
