922507-06-0 Usage
Indole ring
A five-membered aromatic ring system with a nitrogen atom at one position.
Carboxyl group
A functional group consisting of a carbonyl group (C=O) and a hydroxyl group (-OH) bonded to the same carbon atom.
Bromine atom
A halogen atom with the element symbol Br, providing a bromo substituent to the molecule.
Chloroalkene group
A vinyl group (CH=CH2) with a chlorine atom attached, providing a chlorinated alkenyl substituent to the molecule.
Phenylmethoxy group
A phenyl ring (a six-membered aromatic ring system with delocalized pi electrons) bonded to a methoxy group (-OCH3).
Ethyl ester functional group
A functional group consisting of an ethoxy group (-OCH2CH3) bonded to a carbonyl group (C=O).
Pharmaceutical and chemical research use
The compound is used as a building block for the synthesis of various bioactive molecules.
Specific chemical properties and reactivity
The compound has unique chemical properties and reactivity due to its complex structure, making it valuable for the development of new drugs and materials.
Check Digit Verification of cas no
The CAS Registry Mumber 922507-06-0 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 6 respectively.
Calculate Digit Verification of CAS Registry Number 922507-06:
(8*9)+(7*2)+(6*2)+(5*5)+(4*0)+(3*7)+(2*0)+(1*6)=150
150 % 10 = 0
So 922507-06-0 is a valid CAS Registry Number.
922507-06-0Relevant 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.
