71653-64-0 Usage
Description
2-(DIFLUOROMETHOXY)BENZALDEHYDE is an organic compound that serves as a crucial intermediate in the synthesis of various chemical compounds. It is characterized by the presence of a difluoromethoxy group attached to a benzene ring, with an aldehyde functional group. This unique structure endows it with versatile reactivity and makes it a valuable building block in the production of pharmaceuticals, agrochemicals, and dyestuffs.
Uses
Used in Pharmaceutical Industry:
2-(DIFLUOROMETHOXY)BENZALDEHYDE is used as an intermediate for the preparation of pharmaceuticals. Its unique structure allows it to be a key component in the synthesis of various drug molecules, contributing to the development of new medications with improved therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 2-(DIFLUOROMETHOXY)BENZALDEHYDE is utilized as a starting material for the synthesis of agrochemicals. Its involvement in the production of these chemicals helps in the development of effective pesticides, herbicides, and other agricultural products that enhance crop protection and yield.
Used in Dye Industry:
2-(DIFLUOROMETHOXY)BENZALDEHYDE is employed as a raw material in the dye industry. Its chemical properties make it suitable for the synthesis of various dyes, which are used in a wide range of applications, including textiles, plastics, and printing inks.
Used in the Synthesis of 1,4-Dihydropyridine Derivatives:
2-(DIFLUOROMETHOXY)BENZALDEHYDE is used as a starting reagent in the synthesis of 4-(2-difluoromethoxyphenyl)-substituted 1,4-dihydropyridine 3,5-diesters. These compounds have potential applications in various fields, including pharmaceuticals and materials science.
Used in the Synthesis of Other Compounds:
2-(DIFLUOROMETHOXY)BENZALDEHYDE may also be used as a starting reagent in the synthesis of several other compounds, such as:
1. 2-[2-(DIFLUOROMETHOXY)BENZYLIDENE]METHYL ACETOACETATE
2. 3-(2-CYANOETHYL) 5-(2-PROPOXYETHYL) 4-[2-(DIFLUOROMETHOXY)PHENYL]-2,6-DIMETHYL-1,4-DIHYDRO-3,5-PYRIDINEDICARBOXYLATE
3. 2-PROPOXYETHYL 5-CYANO-4-[2-(DIFLUOROMETHOXY)PHENYL]-2-METHYL-6-THIOXO-1,4,5,6-TETRAHYDROPYRIDINE-3-CARBOXYLATE
4. METHYL 5-CYANO-4-(2-DIFLUOROMETHOXYPHENYL)-2-METHYL-6-THIOXO-1,4,5,6-TETRAHYDROPYRIDINE-3-CARBOXYLATE
These synthesized compounds can have various applications, depending on their specific properties and the industries they are tailored for.
Check Digit Verification of cas no
The CAS Registry Mumber 71653-64-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,6,5 and 3 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 71653-64:
(7*7)+(6*1)+(5*6)+(4*5)+(3*3)+(2*6)+(1*4)=130
130 % 10 = 0
So 71653-64-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H6F3NOS/c10-9(11,12)5-1-2-7-6(3-5)13-8(14)4-15-7/h1-3H,4H2,(H,13,14)
71653-64-0Relevant articles and documents
SYNTHESIS OF DIFLUOROMETHYL ETHERS AND SULFIDES
-
Paragraph 0076; 0078-0082, (2014/07/22)
The synthesis of difluoromethyl ethers and sulfides with a simple, non-ozone- depleting reagent is described. The difluoromethylation of phenols with this reagent occurs at room temperature within minutes with exceptional functional group tolerance. The mild conditions makes possible tandem processes for the conversion of aryl boronic acids, aryl halides and arenes to difluoromethyl ethers. Mechanistic studies support a reaction pathway involving nucleophilic attack of the phenolate to difluorocarbene.
Pharmaceutical uses for fluoroalkoxybenzylamino derivatives of nitrogen containing heterocycles
-
, (2008/06/13)
The present invention relates to methods of treating various CNS and other disorders by adminstering fluoroalkoxybenzylamino derivatives of nitrogen containing heterocyclic compounds, and specifically, by administering compounds of the formula wherein Q,
FLUOROALKOXYBENZYLAMINO DERIVATIVES OF NITROGEN CONTAINING HETEROCYCLES
-
, (2008/06/13)
The present invention relates to novel fluoroalkoxybenzylamino derivatives of nitrogen containing heterocyclic compounds, and specifically, to compounds of the formula STR1 wherein Q, X 1, x. sup.2 and X 3 are as defined below. These novel compounds are u
