73219-92-8 Usage
General Description
3-BROMO-5-CHLORO-2,6-DIMETHOXYBENZOIC ACID is a chemical compound that belongs to the class of benzoic acids. It is a white to light yellow crystalline powder with a molecular formula C9H8BrClO4. 3-BROMO-5-CHLORO-2,6-DIMETHOXYBENZOIC ACID is commonly used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and dyes. It has potential applications in the development of new drugs for various therapeutic purposes due to its pharmacological properties. The compound's unique structure and reactivity make it an important building block in organic synthesis. Additionally, it is used in the manufacturing of polymers and other industrial products. However, 3-BROMO-5-CHLORO-2,6-DIMETHOXYBENZOIC ACID should be handled 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 articles and documents
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.
