85590-94-9 Usage
Uses
Used in Chemical Synthesis:
N-(6-acetyl-1,3-benzodioxol-5-yl)-2-chloroacetamide is used as a synthetic intermediate for the preparation of various organic compounds. Its chloroacetamide functional group allows for a wide range of chemical reactions, making it a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Drug Development:
Due to the potential biological activity of the benzodioxole moiety, N-(6-acetyl-1,3-benzodioxol-5-yl)-2-chloroacetamide is used as a lead compound in drug discovery. It may serve as a starting point for the development of new therapeutic agents targeting a variety of diseases and conditions. N-(6-acetyl-1,3-benzodioxol-5-yl)-2-chloroacetamide's structure can be further modified to optimize its pharmacological properties, such as potency, selectivity, and bioavailability.
Used in Pharmaceutical Industry:
N-(6-acetyl-1,3-benzodioxol-5-yl)-2-chloroacetamide is used as an active pharmaceutical ingredient (API) for the development of new drugs. Its unique structure and potential biological activity make it a candidate for the treatment of various medical conditions. N-(6-acetyl-1,3-benzodioxol-5-yl)-2-chloroacetamide can be formulated into different dosage forms, such as tablets, capsules, or injectables, to ensure optimal therapeutic efficacy.
Used in Research and Development:
In the field of research and development, N-(6-acetyl-1,3-benzodioxol-5-yl)-2-chloroacetamide is used as a research tool to study the structure-activity relationships of benzodioxole-containing compounds. It can help scientists understand the molecular mechanisms underlying the biological activity of these compounds and guide the design of more effective and safer drugs.
Check Digit Verification of cas no
The CAS Registry Mumber 85590-94-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,5,9 and 0 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 85590-94:
(7*8)+(6*5)+(5*5)+(4*9)+(3*0)+(2*9)+(1*4)=169
169 % 10 = 9
So 85590-94-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H10ClNO4/c1-6(14)7-2-9-10(17-5-16-9)3-8(7)13-11(15)4-12/h2-3H,4-5H2,1H3,(H,13,15)
85590-94-9Relevant academic research and scientific papers
ANTAGONISTS OF T2R54 AND COMPOSITIONS AND USES THEREOF
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Page/Page column 77; 115, (2020/02/29)
The present disclosure generally provides compounds that antagonize certain T2R taste receptors, including related uses, methods, and compositions for the reduction of bitter taste and/or the enhancement of sweet taste. In certain aspects, the disclosure provides flavored articles or flavored compositions comprising such compounds, as well as uses of such compounds to reduce the bitter taste and/or enhance the sweet taste of such flavored articles or flavored compositions.
THE SYNTHESIS OF SOME COMPLEX QUINAZOLINE DERIVATIVES CONTAINING ONE OR TWO QUINAZOLINE RINGS AND CARRYING AMINO, ACYLAMINO, ESTER AND/OR CARBAMATE FUNCTIONAL GROUPS IN THEIR SIDE CHAINS
Bertha, F.,Fetter, J.,Lempert, K.,Moeller, J.
, p. 213 - 224 (2007/10/02)
The scope of the Bischler synthesis has been extented to the synthesis of complex quinazoline derivatives 3b-3d, 5a-5f, 6a, 6b, 7 and 8.Reductive cleavage of the C-N bond of all 4-(N-monosubstituted aminomethyl)quinazolines tested took place on treatment with ethanol in the presence of acids or bases.
