922507-03-7 Usage
Indole moiety
A five-membered aromatic ring system with a nitrogen atom at one end, contributing to potential biological activity and binding properties.
Carboxylic acid group
A functional group consisting of a carbonyl group (C=O) and a hydroxyl group (-OH) on the same carbon atom, contributing to acidity and potential binding properties.
Ethyl ester group
A functional group formed by the esterification of the carboxylic acid group with ethanol, contributing to reduced acidity and potential reactivity with nucleophiles.
Phenylmethoxy group
A phenyl ring substituted with a methoxy group (-OCH3), contributing to steric hindrance and potential electronic effects.
Chloro-propenyl group
A propenyl group (a three-carbon chain with a double bond between the first two carbons) with a chlorine atom attached to the second carbon, contributing to potential reactivity and halogen bonding.
Iodine atom
A halogen atom attached to the phenyl ring, contributing to potential reactivity and the ability to participate in halogen bonding.
Biological activity
Potential for interaction with biological targets, such as enzymes or receptors, due to the presence of multiple functional groups and a complex structure.
Organic synthesis
May be used as a building block for more complex molecules due to the presence of reactive functional groups.
Handling and use
Specific properties, uses, and potential hazards should be thoroughly researched and understood before handling or using this chemical in any capacity.
Check Digit Verification of cas no
The CAS Registry Mumber 922507-03-7 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 3 respectively.
Calculate Digit Verification of CAS Registry Number 922507-03:
(8*9)+(7*2)+(6*2)+(5*5)+(4*0)+(3*7)+(2*0)+(1*3)=147
147 % 10 = 7
So 922507-03-7 is a valid CAS Registry Number.
922507-03-7Relevant 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 (2007/10/03)
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.
