320-72-9 Usage
Description
3,5-Dichlorosalicylic acid is a bio-active drug characterized by its white crystalline powder form. It is known for its interaction with a model transport protein, bovine serum albumin, and has been identified as a potential inhibitor of human 20α-hydroxysteroid dehydrogenase.
Uses
Used in Pharmaceutical Industry:
3,5-Dichlorosalicylic acid is used as a bio-active compound for its potential role in inhibiting human 20α-hydroxysteroid dehydrogenase, which can be significant in the development of treatments for various medical conditions.
Used in Chemical Industry:
3,5-Dichlorosalicylic acid is used as an intermediate in the production of dyes, leveraging its chemical properties to contribute to the synthesis of a range of dye products.
Used in Medicine:
3,5-Dichlorosalicylic acid is utilized as a pharmaceutical intermediate, playing a crucial role in the development of new medicines that can address specific health concerns.
Safety Profile
Poison by
intraperitoneal route. When heated to
decomposition it emits toxic fumes of Cl-.
Check Digit Verification of cas no
The CAS Registry Mumber 320-72-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,2 and 0 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 320-72:
(5*3)+(4*2)+(3*0)+(2*7)+(1*2)=39
39 % 10 = 9
So 320-72-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H4Cl2O3/c8-3-1-4(7(11)12)6(10)5(9)2-3/h1-2,10H,(H,11,12)/p-1
320-72-9Relevant articles and documents
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Datta
, p. 2037 (1919)
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Sodium lauryl sulfate-catalyzed oxidative chlorination of aromatic compounds
Mahajan, Tanu,Kumar, Lalit,Dwivedi, K.,Agarwal, D. D.
, p. 3655 - 3663,9 (2020/08/31)
Chlorination of commercially important aromatic compounds using sodium chloride as chlorine source and sodium periodate as oxidant in acidic medium catalyzed by sodium lauryl sulfate (SLS) led to the chloro-substituted aromatics in good yields and purity. Addition of sodium lauryl sulfate led to increased chlorination rate, better yield, excellent purity, and better quality of end product. The advantages of the present method are greater yield, excellent purity, and shorter reaction time at room temperature. Also dichlorinated product can be obtained by increasing the amount of sodium chloride and sodium periodate at slightly higher temperature (40C).
Acyl derivatives of 2-aminobenzimidazole and their fungicide activity
Pilyugin,Sapozhnikov,Sapozhnikova
, p. 738 - 743 (2007/10/03)
Procedures have been developed for the preparation of methyl 2-benzimidazolylcarbamate, 2-acetylaminobenzimidazole, 2- benzoylaminobenzimidazole, 2-(3,5-dibromo-2-hydroxybenzoylamino)benzimidazole, 1-(3,6-dichloro-2-methoxybenzoyl)-2-aminobenzimidazole, 2-(3,5-dichloro-2- hydroxybenzoylamino)benzimidazole, 2-(3,5-dichloro-2-methoxybenzoylamino) benzimidazole, and 1-(3,5,6-trichloro-2-methoxybenzoyl)-2-aminobenzimidazole. The synthesized compounds have been tested for fungicide activity.
