39533-43-2 Usage
Uses
Used in Organic Synthesis:
AMINO-BENZO[1,3]DIOXOL-5-YL-ACETIC ACID is used as a building block in organic synthesis for the creation of various chemical compounds. Its unique structure and functional groups facilitate the formation of new molecules with diverse properties.
Used in Pharmaceutical Development:
In the pharmaceutical industry, AMINO-BENZO[1,3]DIOXOL-5-YL-ACETIC ACID is used as a key intermediate in the development of new drugs and medicinal compounds. Its presence in these formulations is attributed to its potential to contribute to the therapeutic effects of the final product.
Used in Medicinal Chemistry Research:
AMINO-BENZO[1,3]DIOXOL-5-YL-ACETIC ACID is utilized as a subject of study in medicinal chemistry to explore its biological activities and understand its interactions with biological systems. This research is crucial for identifying its potential as a therapeutic agent and for uncovering new avenues for drug discovery.
Used in Pharmacology Studies:
In pharmacology, AMINO-BENZO[1,3]DIOXOL-5-YL-ACETIC ACID is employed to investigate its pharmacological properties, such as its mechanism of action, efficacy, and safety. This helps in assessing its suitability for clinical use and in determining the optimal conditions for its application in treatment regimens.
Check Digit Verification of cas no
The CAS Registry Mumber 39533-43-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,5,3 and 3 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 39533-43:
(7*3)+(6*9)+(5*5)+(4*3)+(3*3)+(2*4)+(1*3)=132
132 % 10 = 2
So 39533-43-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H9NO4/c10-8(9(11)12)5-1-2-6-7(3-5)14-4-13-6/h1-3,8H,4,10H2,(H,11,12)
39533-43-2Relevant academic research and scientific papers
8-hydroxy-7-substituted quinolines as anti-viral agents
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, (2008/06/13)
The present invention provides for 8-hydroxy-7-substituted quinoline compounds such as formula III These compounds are useful as anti-viral agents. Specifically, these compounds have anti-viral activity against the herpes virus, cytomegalovirus (CMV). Many of these compounds are also active against other herpes viruses, such as the varicella zoster virus, the Epstein-Barr virus, the herpes simplex virus and the human herpes virus type 8 (HHV-8).
A facile synthesis of substituted phenylglycines
Davies, Antony J.,Ashwood, Michael S.,Cottrell, Ian F.
, p. 1095 - 1102 (2007/10/03)
A convenient scaleable process for the preparation of substituted phenylglycines 2 by a modified Strecker reaction is described. Bisulfite- mediated addition of benzylamine and cyanide anion to substituted benzaldehydes 3 gave the aminonitriles 4 which were hydrolysed in two steps to the N-protected amino acid 1. Debenzylation using catalytic transfer hydrogenation gave the title compounds in good yield.
Orally Active Cephalosporins and Penicillins
Boehme, E. H. W.,Bambury, R. E.,Baumann, R. J.,Erickson, R. C.,Harrison, B. L.,et al.
, p. 405 - 412 (2007/10/02)
A number of orally active cephalosporins and penicillins with interesting biological activity were synthesized.Two of these, 7-glycyl>amino>deacetoxycephalosporanic acid and 7-amino>deacetoxycephalosporanic acid were considerably more active than cephalexin both in vitro and in vivo against staphylococcal and streptococcal infections.
