40359-59-9 Usage
Uses
Used in Pharmaceutical Industry:
2-(3-CHLOROBENZYLOXY)BENZALDEHYDE is used as an intermediate in organic synthesis for the production of pharmaceuticals. Its unique structure and properties make it a valuable component in the development of new medications.
Used in Dye Industry:
In the dye industry, 2-(3-CHLOROBENZYLOXY)BENZALDEHYDE is used as a precursor in the synthesis of various dyes. Its chemical properties contribute to the creation of dyes with specific color characteristics and stability.
Used in Fine Chemicals Production:
2-(3-CHLOROBENZYLOXY)BENZALDEHYDE is utilized in the production of other fine chemicals, where its unique chemical structure and reactivity are essential for the synthesis of high-quality specialty chemicals.
Used in Antimicrobial Agents Development:
2-(3-CHLOROBENZYLOXY)BENZALDEHYDE is used as an active ingredient in the development of new antimicrobial agents due to its potent antifungal and antibacterial properties. Its ability to inhibit the growth of various microorganisms makes it a valuable component in creating effective medications and treatments.
Used in Fragrance and Flavor Compounds Manufacturing:
In the fragrance and flavor industry, 2-(3-CHLOROBENZYLOXY)BENZALDEHYDE is used for its aromatic characteristics and strong odor. It serves as a key component in the creation of various fragrances and flavor compounds, enhancing their sensory properties and appeal.
Check Digit Verification of cas no
The CAS Registry Mumber 40359-59-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,3,5 and 9 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 40359-59:
(7*4)+(6*0)+(5*3)+(4*5)+(3*9)+(2*5)+(1*9)=109
109 % 10 = 9
So 40359-59-9 is a valid CAS Registry Number.
InChI:InChI=1/C14H11ClO2/c15-13-6-3-4-11(8-13)10-17-14-7-2-1-5-12(14)9-16/h1-9H,10H2
40359-59-9Relevant academic research and scientific papers
Hydride transfer reactions of 5-(2-alkohybenzylidene) barbituric acids: Synthesis of 2,4,6-trioxoperhydropyrimidine-5-spiro-3′-chromanes
Krasnov, Konstantin A.,Dorovatovskii, Pavel V.,Zubavichus, Yan V.,Timofeeva, Tatiana V.,Khrustalev, Victor N.
, p. 542 - 549 (2017/01/12)
The thermal cyclization of 5-(2-phenoxymethylphenyl-methylene)barbituric acid and its derivatives affords 2,4,6-trioxoperhydropyrimidine-5-spiro-3′-chromanes. The reactions require no catalysts and proceed at temperatures from 118 to 240?°C depending on the substrate activity. These cyclization reactions are analogous to T-reactions of tertiary amines involving the hydride transfer.
Synthesis of heterocycles with MF/Al2O3 base-systems: 2-arylbenzofuranes and 2,3-diarylisoquinolin-1(2H)-ones
Hellwinkel,Goke
, p. 1135 - 1141 (2007/10/02)
2-Benzyloxybenzaldehydes, -acetophenones and -benzophenones substituted in the benzyl part with electron-withdrawing groups, cyclize easily to 2-arylbenzofuranes by using a standardized KF- or CsF-Al2O3 base system. An efficient one-pot synthesis for 2,3-diarylisoquinolin-1(2H)-ones is possible by reacting a variety of arene carbaldehyde anils with phthalides under the same reaction conditions.
