40359-59-9 Usage
General Description
2-(3-chlorobenzyloxy)benzaldehyde is a chemical compound with a formula of C14H11ClO2. It is a benzaldehyde derivative with a chlorobenzyloxy group attached to the second position of the benzene ring. 2-(3-CHLOROBENZYLOXY)BENZALDEHYDE is commonly used in organic synthesis for the production of pharmaceuticals, dyes, and other fine chemicals. It is also known for its potent antifungal and antibacterial properties, making it a valuable ingredient in the development of new medications and antimicrobial agents. Additionally, 2-(3-chlorobenzyloxy)benzaldehyde is used in the manufacturing of fragrance and flavor compounds due to its aromatic characteristics and strong odor.
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 articles and documents
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.
