86483-52-5 Usage
Description
(Z)-2-(2,4-DICHLORO-5-FLUORO-BENZOYL)-3-ETHOXY-ACRYLIC ACID ETHYL ESTER is a chemical compound featuring a molecular structure that includes a benzoyl group, a fluorine atom, two chlorine atoms, and an ethoxy group. This ethyl ester derivative is recognized for its potential pharmaceutical properties and is widely utilized in organic synthesis and drug development. Its unique molecular composition positions it as a significant building block in the field of organic chemistry, with possible applications in the development of innovative materials and technologies.
Uses
Used in Pharmaceutical Industry:
(Z)-2-(2,4-DICHLORO-5-FLUORO-BENZOYL)-3-ETHOXY-ACRYLIC ACID ETHYL ESTER is used as a key intermediate for the production of various pharmaceuticals. Its unique molecular structure contributes to the development of new drugs with potential therapeutic benefits.
Used in Agrochemical Industry:
In the agrochemical industry, (Z)-2-(2,4-DICHLORO-5-FLUORO-BENZOYL)-3-ETHOXY-ACRYLIC ACID ETHYL ESTER is used as a crucial component in the synthesis of different agrochemicals, such as pesticides and herbicides, due to its potential to enhance their effectiveness and target-specific action.
Used in Organic Chemistry:
(Z)-2-(2,4-DICHLORO-5-FLUORO-BENZOYL)-3-ETHOXY-ACRYLIC ACID ETHYL ESTER serves as an important building block in organic chemistry, facilitating the synthesis of complex organic molecules and contributing to the advancement of chemical research and development.
Used in Material Science and Technology Development:
This chemical compound may also have potential applications in the development of new materials and technologies, thanks to its unique chemical properties, which could lead to innovative solutions in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 86483-52-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,4,8 and 3 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 86483-52:
(7*8)+(6*6)+(5*4)+(4*8)+(3*3)+(2*5)+(1*2)=165
165 % 10 = 5
So 86483-52-5 is a valid CAS Registry Number.
86483-52-5Relevant articles and documents
ANTIVIRAL AND ANTIMICROBIAL COMPOUNDS
-
, (2014/03/25)
Disclosed are guanidine and biguanidine derivatives which have anti-viral and antibacterial activity. Also disclosed are pharmaceutical compositions containing such compounds as an active ingredient, and anti-viral and anti-bacterial methods utilizing such compounds. Methods of treating infections using the guanidine and biguanidine derivatives are also disclosed.
Synthesis and antibacterial activity of 1-(substituted pyrrolyl)-7- (substituted amino)-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acids
Liu,Guo
, p. 3469 - 3473 (2007/10/02)
Seventeen quinolone compounds characterized by having a fluorine atom at the 6-position, a substituted amino at the 7-position, and a substituted pyrrolyl at the 1-position were synthesized for the first time. The in vitro antibacterial activities of thes
Synthesis and Structure-Activity Relationships of Novel Arylfluoroquinolone Antibacterial Agents
Chu, Daniel T. W.,Fernandes, Prabhavathi B.,Claiborne, Akiyo K.,Pihuleac, Eva,Nordeen, Carl W.,et al.
, p. 1558 - 1564 (2007/10/02)
A series of novel arylfluoroquinolones has been prepared.These derivatives are characterized by having a fluorine atom at the 6-position, substituted amino groups at the 7-position, and substituted phenyl groups at the 1-position.Structure-activity relationship (SAR) studies indicate that the in vitro antibacterial potency is greatest when the 1-substituent is either p-fluorophenyl or p-hydroxyphenyl and the 7-substituent is either 1-piperazinyl, 4-methyl-1-piperazinyl, or 3-amino-1-pyrrolidinyl.The electronic and spatial properties of the 1-substituent, as well as the steric bulk, play important roles in the antimicrobial potency in this class of antibacterials.As a result of this study, compounds 45 and 41 were found to possess excellent in vitro potency and in vivo efficacy.
