73178-79-7 Usage
Uses
Used in Pharmaceutical Synthesis:
2-BIPHENYL-3'-CHLORO-CARBOXYLIC ACID is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with specific therapeutic properties, making it valuable in the pharmaceutical industry.
Used in Agrochemical Production:
In the agrochemical industry, 2-BIPHENYL-3'-CHLORO-CARBOXYLIC ACID serves as an essential building block for the creation of new agrochemicals. Its reactivity and ability to form complex structures enable the development of innovative products with improved efficacy and selectivity in crop protection.
Used in Dye and Pigment Manufacturing:
2-BIPHENYL-3'-CHLORO-CARBOXYLIC ACID is employed as an intermediate in the production of dyes and pigments. Its chemical properties allow for the synthesis of a wide range of colorants used in various applications, such as textiles, plastics, and printing inks.
Used in Medicinal Chemistry Research:
2-BIPHENYL-3'-CHLORO-CARBOXYLIC ACID is utilized as a subject of interest in medicinal chemistry research. Its potential pharmacological and biological activities make it a promising candidate for the development of new therapeutic agents and the exploration of novel chemical space in drug discovery.
Check Digit Verification of cas no
The CAS Registry Mumber 73178-79-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,1,7 and 8 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 73178-79:
(7*7)+(6*3)+(5*1)+(4*7)+(3*8)+(2*7)+(1*9)=147
147 % 10 = 7
So 73178-79-7 is a valid CAS Registry Number.
73178-79-7Relevant academic research and scientific papers
Reactions of 1,5-Dichloroanthrachinone with Nucleophiles
Ruediger, Edward H.,Kaldas, Magdy L.,Ghandi. Sham S.,Fedryna, Cristi,Gibson, Martin S.
, p. 1974 - 1978 (2007/10/02)
Reactions of 1,5-dichloroanthraquinone (1) with various nucleophiles were examined to evaluate possibilities for selective substitution. 1-Amino-5-chloroanthraquinone was obtained from 1 by reaction with (a) sodium azide in dimethyl sulfoxide and (b ammonia in the presence of potassium fluoride, but 1 with potassium in ammonia gave 3-chlorobenzoic acid.Conditions were found for preferential substitution in reactions of 1 with (c) 4-toluidine, (d) hexamethylphosphoric triamide, and (e) N-methylformamide.Reagent e is preferred for making 1-chloro-5-(methylamino)anthraquinone, though this compound predominates in mixtures produced when d is used.Potassium hydroxide in 2-ethoxyethanol converts 1 to the corresponding mono- and diethers of 1,5-dihydroxyanthraquinone, while sodium hydrosulfide and 1 give bis(5-chloroanthraquinonyl)sulfide.
