73219-92-8 Usage
Uses
Used in Pharmaceutical Industry:
3-BROMO-5-CHLORO-2,6-DIMETHOXYBENZOIC ACID is used as an intermediate in the synthesis of pharmaceuticals for its potential applications in the development of new drugs for various therapeutic purposes. Its pharmacological properties contribute to its significance in this field.
Used in Agrochemical Industry:
In the agrochemical industry, 3-BROMO-5-CHLORO-2,6-DIMETHOXYBENZOIC ACID serves as an intermediate, playing a crucial role in the synthesis of agrochemicals that are vital for agricultural applications.
Used in Dye Manufacturing:
3-BROMO-5-CHLORO-2,6-DIMETHOXYBENZOIC ACID is also utilized in the manufacturing of dyes, where its chemical properties are essential for creating a wide range of colorants used in various industries.
Used in Polymer Production:
3-BROMO-5-CHLORO-2,6-DIMETHOXYBENZOIC ACID is used in the manufacturing of polymers and other industrial products, highlighting its versatility and importance in diverse sectors.
Safety Note:
It is important to handle 3-BROMO-5-CHLORO-2,6-DIMETHOXYBENZOIC ACID with care and in accordance with proper safety protocols due to its potential health hazards.
Check Digit Verification of cas no
The CAS Registry Mumber 73219-92-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,2,1 and 9 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 73219-92:
(7*7)+(6*3)+(5*2)+(4*1)+(3*9)+(2*9)+(1*2)=128
128 % 10 = 8
So 73219-92-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H8BrClO4/c1-14-7-4(10)3-5(11)8(15-2)6(7)9(12)13/h3H,1-2H3,(H,12,13)/p-1
73219-92-8Relevant academic research and scientific papers
Potential Neuroleptic Agents. 2,6-Dialkoxybenzamide Derivatives with Potent Dopamine Receptor Blocking Activities
Florvall, Lennart,Oegren, Sven-Ove
, p. 1280 - 1286 (2007/10/02)
A series of some novel N-(1-ethyl-2-pyrrolidinylmethyl)benzamides was synthesized and tested for dopamine receptor blockade in vivo by the ability to block the apomorphine syndrome in the rat.Several compounds were considerably more potent than sulpiride as dopamine receptor blockers and displayed low liability to induce extrapyramidal side effects (catalepsy) in the rat.The blockade of dopamine receptor activity in vivo was mainly confined to the levorotatory isomers having the S absolute configuration.The structure-activity relationships are discussed.
2,6-Dialkoxybenzamides, intermediates, pharamaceutical compositions and methods for treatment of psychotic disorders
-
, (2008/06/13)
A compound of the formula, wherein R1 is an alkyl group with 1-3 carbon atoms, R2 and R3 are the same or different and each is hydrogen, chlorine or bromine; and pharmaceutically acceptable salts and optical isomers thereof; methods and intermediates for
