5803-67-8 Usage
Uses
Used in Pharmaceutical Industry:
2-CHLORO-1-(5,6,7,8-TETRAHYDRONAPHTHALEN-2-YL)ETHANONE is used as a building block in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs with potential therapeutic effects.
Used in Agrochemical Industry:
In the agrochemical sector, 2-CHLORO-1-(5,6,7,8-TETRAHYDRONAPHTHALEN-2-YL)ETHANONE serves as a key intermediate in the production of agrochemicals, aiding in the creation of effective pest control agents and other agricultural chemicals.
Used in Fine Chemicals Synthesis:
2-CHLORO-1-(5,6,7,8-TETRAHYDRONAPHTHALEN-2-YL)ETHANONE is utilized as a reagent in organic chemistry synthesis reactions, playing a crucial role in the formation of various fine chemicals with specific applications.
Used in Material Science:
2-CHLORO-1-(5,6,7,8-TETRAHYDRONAPHTHALEN-2-YL)ETHANONE may have potential uses in the development of new materials and chemical compounds, owing to its distinctive structure and properties that could contribute to advancements in material science.
Check Digit Verification of cas no
The CAS Registry Mumber 5803-67-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,0 and 3 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5803-67:
(6*5)+(5*8)+(4*0)+(3*3)+(2*6)+(1*7)=98
98 % 10 = 8
So 5803-67-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H13ClO/c13-8-12(14)11-6-5-9-3-1-2-4-10(9)7-11/h5-7H,1-4,8H2
5803-67-8Relevant academic research and scientific papers
N-(4-Substituted-thiazolyl)oxamic Acid Derivatives, a New Series of Potent, Orally Actve Antiallergy Agents
Hargrave, Karl D.,Hess, Friedrich K.,Oliver, James T.
, p. 1158 - 1163 (2007/10/02)
A series of N-(4-substituted-thiazolyl)oxamic acid derivatives were synthesized and tested for antiallergy activity in the rat PCA model.These compounds were conveniently prepared by treatment of the appropriate acetophenone with thiourea and iodine or by reaction of the chloroacetylbenzene with thiourea to give the corresponding aminothiazoles; subsequent condensation with ethyloxalyl chloride gave the thiazolyloxamates.Many of the analogues showed a 50percent inhibition at oxamic acid ethanolamine salt (61, PRH-836-EA), has been selected for further pharmacological evaluation.
