4770-34-7 Usage
Uses
Used in Pharmaceutical Synthesis:
1-(6-hydroxyindolin-1-yl)ethanone is utilized as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs with potential therapeutic applications.
Used in Organic Chemistry Research:
As a building block, 1-(6-hydroxyindolin-1-yl)ethanone is used in the preparation of various organic compounds, facilitating the advancement of organic chemistry through the creation of novel molecules and materials.
Used in Biological Activity Studies:
1-(6-hydroxyindolin-1-yl)ethanone is employed in research to explore its potential biological activities, which may include pharmacological properties that could be harnessed for therapeutic purposes.
Check Digit Verification of cas no
The CAS Registry Mumber 4770-34-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,7 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4770-34:
(6*4)+(5*7)+(4*7)+(3*0)+(2*3)+(1*4)=97
97 % 10 = 7
So 4770-34-7 is a valid CAS Registry Number.
4770-34-7Relevant academic research and scientific papers
NEAR-INFRARED NERVE-SPARING FLUOROPHORES
-
, (2020/02/17)
Provided are far red to near-infrared nerve-sparing fluorescent compounds, compositions comprising them, and methods of their use in medical procedures.
NERVE-SPECIFIC FLUOROPHORE FORMULATIONS FOR DIRECT AND SYSTEMIC ADMINISTRATION
-
, (2020/03/02)
Nerve-specific fluorophore formulations for direct or systemic administration are described. The formulations can be used in fluorescence-guided surgery (FGS) to aid in nerve preservation during surgical interventions.
Photo-induced rearrangement of 1-ethoxy-2-phenylindole
Yamada, Koji,Somei, Masanori
, p. 2481 - 2484 (2007/10/03)
Photoirradiation of 1-ethoxy-2-phenylindole in methanol afforded 3- and 6-ethoxy-2-phenylindoles. The structural determination of the latter is carried out by direct comparison of its spectral data with those of the authentic 4-, 5-, 6-, and 7-ethoxy-2-phenylindoles, whose syntheses are also included.
