922507-01-5 Usage
Molecular structure
1H-Indole-2-carboxylic acid, 7-bromo-4-(phenylmethoxy)-1-(2-propyn-1-yl)-, ethyl ester has a complex molecular structure that includes an indole ring with various substituents.
Indole ring
The core structure of the compound is an indole ring, which is a bicyclic aromatic system consisting of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring.
Carboxylic acid substitution
The indole ring is substituted with a carboxylic acid group (-COOH) at position 2, which contributes to the compound's acidity and may be involved in hydrogen bonding and other interactions.
Bromine atom
A bromine atom (Br) is attached at position 7 of the indole ring, which may influence the compound's lipophilicity, electronic properties, and potential biological activity.
Propargyl substituent
A 1-(2-propyn-1-yl) group, which is an alkyne with a triple bond between the first and second carbon atoms, is present in the molecule. This group may be involved in click chemistry reactions and other applications.
Ethyl ester functional group
The carboxylic acid group is further functionalized as an ethyl ester (-COOEt), which may improve the compound's lipophilicity and membrane permeability.
Potential applications
1H-Indole-2-carboxylic acid, 7-bromo-4-(phenylmethoxy)-1-(2-propyn-1-yl)-, ethyl ester has potential applications in pharmaceutical research and development due to its unique structure and properties.
Biological activity
The compound's biological activity and potential therapeutic uses are not yet fully understood and require further research to explore its effects and potential applications.
Need for further research
To fully understand the potential uses and effects of 1H-Indole-2-carboxylic acid, 7-bromo-4-(phenylmethoxy)-1-(2-propyn-1-yl)-, ethyl ester, additional studies and investigations are necessary.
Check Digit Verification of cas no
The CAS Registry Mumber 922507-01-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,2,5,0 and 7 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 922507-01:
(8*9)+(7*2)+(6*2)+(5*5)+(4*0)+(3*7)+(2*0)+(1*1)=145
145 % 10 = 5
So 922507-01-5 is a valid CAS Registry Number.
922507-01-5Relevant articles and documents
Cyclization of free radicals at the C-7 position of ethyl indole-2-carboxylate derivatives: An entry to a new class of duocarmycin analogues
Al-Said, Naim H.,Shawakfeh, Khaled Q.,Abdullah, Wasim N.
, p. 1446 - 1457 (2005)
Aryl free-radicals generated at the C-7 position of ethyl indole-2-carboxylates bearing N-allyl and propargylic groups triggered intramolecular cyclizations to furnish a new class of Duocarmycin analogues, formal ethyl pyrrolo[3,2,1-ij]quinoline-2-carboxylate derivatives, through the less favorable 6-endo-trig cyclization mode.
