3470-49-3 Usage
Uses
Used in Chemical Synthesis:
5-Hydroxy-1-indanone is used as a starting material in the multi-step synthesis of 5H-indeno[1,2-c]pyridazin-5-one analogs. These analogs have potential applications in pharmaceutical and chemical industries.
Used in Pharmaceutical Industry:
5-Hydroxy-1-indanone may be used in the preparation of (5-hydroxy-indan-(1E)-ylidene)-acetic acid and 5-[2-(phenyl)ethoxy]-1-indanone. These compounds have potential applications as pharmaceutical agents, with potential therapeutic properties.
Used in Chemical Research:
5-Hydroxy-1-indanone is also used as a research compound in the field of organic chemistry. It can be used to study the reactivity and properties of various functional groups and to develop new synthetic methods and strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 3470-49-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,7 and 0 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3470-49:
(6*3)+(5*4)+(4*7)+(3*0)+(2*4)+(1*9)=83
83 % 10 = 3
So 3470-49-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H8O2/c10-7-2-3-8-6(5-7)1-4-9(8)11/h2-3,5,10H,1,4H2
3470-49-3Relevant academic research and scientific papers
Synthesis and evaluation of dimeric 1,2,3,4-Tetrahydro-naphthalenylamine and Indan-1-ylamine derivatives with mast cell-stabilising and anti-allergic activity
Barlow, James W.,Walsh, John J.
experimental part, p. 25 - 37 (2010/03/04)
In a continuation of our studies into 4-Amino-3,4-dihydro-2H-naphthalen-1-ones as novel modulators of allergic and inflammatory phenomena, we have extended our work to include dimeric analogues. Of these derivatives, the most promising activity was seen with tertiary amine 58a, which exhibited potent mast cell-stabilising activity in vitro against a variety of stimuli and also in vivo against passive cutaneous anaphylaxis.
3-NITROCYCLOALKENONES, SYNTHESIS AND USE AS REVERSE AFFINITY CYCLOALKYNONE EQUIVALENTS
Corey, E. J.,Estreicher, Herbert
, p. 603 - 606 (2007/10/02)
A partical synthesis of 3-nitrocycloalkenones and their utilization as dienophiles in the Diels-Alder reaction are discribed.The results demonstrate a reverse affinity equivalency between these β-nitro-enones and "cycloalkynones".
