59794-34-2 Usage
Uses
Used in Pharmaceutical Industry:
3(2H)-Benzothiazoleacetic acid, 2-thioxois used as a key intermediate in the synthesis of various pharmaceuticals. It is particularly valuable in the development of drugs targeting specific biological pathways, such as those involved in inflammation, pain, and other diseases. Its unique chemical structure allows for the creation of novel drug candidates with improved efficacy and selectivity.
Used in Agrochemical Industry:
In the agrochemical industry, 3(2H)-Benzothiazoleacetic acid, 2-thioxois utilized in the synthesis of various agrochemicals, including pesticides and herbicides. Its incorporation into these products can enhance their effectiveness in controlling pests and weeds, leading to increased crop yields and improved agricultural productivity.
Used in Organic Synthesis:
3(2H)-Benzothiazoleacetic acid, 2-thioxoserves as a building block in the synthesis of other organic compounds with useful properties. Its unique structure and reactivity make it a valuable component in the creation of novel molecules with potential applications in various industries, such as materials science, pharmaceuticals, and agrochemicals.
Overall, 3(2H)-Benzothiazoleacetic acid, 2-thioxois a versatile and important chemical compound with a wide range of applications in different industries, particularly in the development of pharmaceuticals and agrochemicals, as well as in organic synthesis. Its unique properties and potential uses make it a valuable asset in the field of chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 59794-34-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,7,9 and 4 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 59794-34:
(7*5)+(6*9)+(5*7)+(4*9)+(3*4)+(2*3)+(1*4)=182
182 % 10 = 2
So 59794-34-2 is a valid CAS Registry Number.
59794-34-2Relevant academic research and scientific papers
A NEW ROUTE TO 2H-(1,2,4)TRIAZINO(3,4b)BENZOTHIAZOLE-3(4H)-ONE (4)
D'Amico, John J.,Bollinger, Frederic G.,Dahl, William E.
, p. 71 - 76 (2007/10/02)
The reaction of 3-(carbethoxymethyl)benzothiazoline-2-thione (1) with excess hydrazine in an aqueous medium at 25-30 deg or 95-100 deg C afforded the hydrazide (3) in 99percent yield and the titled heterocyclic compound (4) in 63percent yield, respectively.Under the same reaction conditions and replacing the above electrophile with 3-(carbethoxymethyl)-2-benzothiazoline furnished the hydrazide (5) in 45percent yield and a 6percent yield of 5 plus a high yield of a resinous mixture, respectively.Possible mechanism and supporting NMR and mass spectral data are discussed.
Synthesis of 2-Thioxo-3-benzothiazolineacetonitrile and Related Products
D'Amico, John J.,Suba, Lydia,Ruminski, Peter G.
, p. 1479 - 1482 (2007/10/02)
Attempts to thermally rearrange 2-benzothiazolylthioacetonitrile (1) to the titled compound 8 failed.The reaction of 3-chloromethyl-2-benzothiazolinethione with potassium cyanide in dimethylformamide (DMF) or dimethylsulfoxide (DMSO) at 25-30 deg C afforded 8 in 98percent yield.Whereas replacing the DMF or DMSO solvent with acetone furnished the unexpected sulfide 9 in 92percent yield.Substituting 3-chloromethyl-2-benzoxazolinethione as the electrophile in the same reaction gave the sulfide 10 in 95percent yield.Possible mechanisms and supporting nmr data are discussed.
