89-45-2 Usage
Description
2-(Sulfooxy)benzoic acid is a benzoic acid derivative characterized by the presence of a sulfooxy group attached to the benzene ring. 2-(Sulfooxy)benzoic acid exhibits acetylcholinesterase inhibitory properties, making it a potential candidate for various applications in different industries.
Uses
Used in Pharmaceutical Industry:
2-(Sulfooxy)benzoic acid is used as a pharmaceutical agent for its acetylcholinesterase inhibitory properties. This characteristic makes it a promising candidate for the development of drugs targeting neurological disorders, such as Alzheimer's disease, where acetylcholinesterase inhibition can help improve cognitive function and memory.
Used in Agrochemical Industry:
In the agrochemical industry, 2-(Sulfooxy)benzoic acid can be utilized as a precursor in the synthesis of various agrochemicals, such as pesticides and herbicides. Its acetylcholinesterase inhibitory properties can be leveraged to develop compounds that target and control pests, thereby enhancing crop protection and yield.
Used in Chemical Research:
2-(Sulfooxy)benzoic acid serves as a valuable compound in chemical research, particularly in the study of benzoic acid derivatives and their potential applications. Researchers can explore its chemical properties, reactivity, and interactions with other molecules to develop new compounds and applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 89-45-2 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 8 and 9 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 89-45:
(4*8)+(3*9)+(2*4)+(1*5)=72
72 % 10 = 2
So 89-45-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H6O6S/c8-7(9)5-3-1-2-4-6(5)13-14(10,11)12/h1-4H,(H,8,9)(H,10,11,12)
89-45-2Relevant articles and documents
Intramolecular Catalysis of Sulphate Diester Hydrolysis by One and Two Carboxy Groups. The Hydrolysis of Aryl 2-Carboxyphenyl Sulphates
Drummond, Jeremy N.,Kirby, Anthony J.
, p. 579 - 584 (2007/10/02)
The hydrolysis of aryl 2-carboxyphenyl (salicyl) sulphates is subject to efficient nucleophilic catalysis by the neighbouring carboxylate group.The intermediate cyclic acyl sulphate can be trapped with hydroxylamine.The reaction of disalicyl sulphate is further catalysed by the second carboxy group, acting, rather inefficiently, as a general acid.
