840538-48-9 Usage
Chemical Family
The compound belongs to the indole family.
Structural Characterization
It is characterized by the presence of a 3-iodo and a 4-(phenylmethoxy) group on the indole ring.
Potential Applications
The compound has potential applications in organic synthesis and medicinal chemistry.
Biological Activities
Indole derivatives have been found to exhibit a wide range of biological activities, including antimicrobial, anticancer, and anti-inflammatory properties.
Influence on Reactivity
The presence of the iodine and phenylmethoxy groups in 1H-Indole, 3-iodo-4-(phenylmethoxy)- may influence its reactivity and interactions with other molecules.
Value in Synthesis
The compound is a valuable building block for the synthesis of new drug candidates or bioactive compounds.
Further Research
Further research and exploration of its properties and applications may lead to the development of novel pharmaceuticals or other valuable products.
Check Digit Verification of cas no
The CAS Registry Mumber 840538-48-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,0,5,3 and 8 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 840538-48:
(8*8)+(7*4)+(6*0)+(5*5)+(4*3)+(3*8)+(2*4)+(1*8)=169
169 % 10 = 9
So 840538-48-9 is a valid CAS Registry Number.
840538-48-9Relevant academic research and scientific papers
INDOLE DERIVATIVES AS ALPHA-1 -ANTITRYPSIN MODULATORS FOR TREATING ALPHA-1 -ANTITRYPSIN DEFICIENCY (AATD)
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Paragraph 00234; 00316; 00350, (2021/10/11)
Indole derivatives as alpha-l-antitrypsin modulators for treating alpha-l-antitrypsin deficiency (AATD).
Indole-glucosides as novel sodium glucose co-transporter 2 (SGLT2) inhibitors. Part 2
Zhang, Xiaoyan,Urbanski, Maud,Patel, Mona,Cox, Geoffrey G.,Zeck, Roxanne E.,Bian, Haiyan,Conway, Bruce R.,Beavers, Mary Pat,Rybczynski, Philip J.,Demarest, Keith T.
, p. 1696 - 1701 (2007/10/03)
A series of indole-O-glucosides and C-glucosides was synthesized and evaluated in SGLT1 and SGLT2 cell-based functional assays. Compounds 2a and 2o were identified as potent SGLT2 inhibitors and screened in ZDF rats.
