1259059-71-6 Usage
Uses
Used in Pharmaceutical Industry:
1-(2-chlorophenyl)-2-(1,2,3,4-tetrazol-2-yl)ethan-1-one is used as a building block for the synthesis of various pharmaceuticals due to its reactivity and versatility. 1-(2-chlorophenyl)-2-(1,2,3,4-tetrazol-2-yl)ethan-1-one's unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, 1-(2-chlorophenyl)-2-(1,2,3,4-tetrazol-2-yl)ethan-1-one is utilized as a key component in the creation of novel agrochemicals. Its chemical properties make it suitable for the development of pesticides, herbicides, and other agricultural products.
Used in Medicinal Chemistry Research:
1-(2-chlorophenyl)-2-(1,2,3,4-tetrazol-2-yl)ethan-1-one is employed as a subject of study in medicinal chemistry research. 1-(2-chlorophenyl)-2-(1,2,3,4-tetrazol-2-yl)ethan-1-one's potential biological activities, attributed to the presence of the 1,2,3,4-tetrazol-2-yl group, make it a promising candidate for the development of new therapeutic agents.
Overall, 1-(2-chlorophenyl)-2-(1,2,3,4-tetrazol-2-yl)ethan-1-one is a versatile and important chemical compound with various potential uses in the fields of chemistry, pharmaceutical science, and agrochemical development.
Check Digit Verification of cas no
The CAS Registry Mumber 1259059-71-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,9,0,5 and 9 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1259059-71:
(9*1)+(8*2)+(7*5)+(6*9)+(5*0)+(4*5)+(3*9)+(2*7)+(1*1)=176
176 % 10 = 6
So 1259059-71-6 is a valid CAS Registry Number.
1259059-71-6Relevant academic research and scientific papers
Method for preparing aryl 2-tetrazol-2-yl ketone with improved selectivity
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Page/Page column 11-12, (2020/04/26)
The present disclosure relates to a method for preparing aryl 2-tetrazol-2-yl ketone of the following Formula 1a with improved selectivity: wherein R1 and R2 are the same as defined herein.
METHOD FOR PREPARATION OF CARBAMIC ACID (R)-1-ARYL-2-TETRAZOLYL-ETHYL ESTER
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, (2011/05/05)
Disclosed is a method for the preparation of carbamic acid (R)-1-aryl-2-tetrazolyl-ethyl ester, comprising the enantioselective enzyme reduction of the corresponding arylketone and the carbamation of the resultant alcohol.
METHOD FOR PREPARATION OF CARBAMIC ACID (R)-1-ARYL-2-TETRAZOLYL-ETHYL ESTER
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Page/Page column 13, (2011/01/12)
Disclosed is a method for the preparation of carbamic acid (R)-1-aryl-2-tetrazolyl-ethyl ester, comprising the asymmetric reduction of arylketone and the carbamation of alcohol.
NEUROTHERAPEUTIC AZOLE COMPOUNDS
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Page/Page column 52-53, (2008/06/13)
Azole compounds containing carbamoyl group and pharmaceutically useful salts thereof are described. The compounds are effective anticonvulsants which are used in the treatment of disorders of the central nervous system, especially as anxiety, depression, convulsion, epilepsy, migraine, bipolar disorder, drug abuse, smoking, ADHD, obesity, sleep disorder, neuropathic pain, stroke, cognitive impairment, neurodegeneration, stroke and muscle spasm.
