314760-17-3 Usage
Bicyclic ring structure
Characteristic of indole compounds
Methoxy group at the 4th position
A methyl group attached to an oxygen atom
Nitroso group at the 7th position
A nitrogen atom bonded to an oxygen atom
Potential reactivity
The nitroso group is known for its reactivity in various chemical reactions
Valuable intermediate
Useful for the synthesis of other organic compounds
Applications in pharmaceutical and material science
Due to its unique structure and reactivity, it has potential uses in these fields.
Check Digit Verification of cas no
The CAS Registry Mumber 314760-17-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,4,7,6 and 0 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 314760-17:
(8*3)+(7*1)+(6*4)+(5*7)+(4*6)+(3*0)+(2*1)+(1*7)=123
123 % 10 = 3
So 314760-17-3 is a valid CAS Registry Number.
314760-17-3Relevant articles and documents
Effects of aromatic substituents on the photocleavage of 1-acyl-7-nitroindolines
Papageorgiou, George,Corrie, John E.T
, p. 8197 - 8205 (2000)
Photolysis of 1-acyl-7-nitroindolines in aqueous solution gives a carboxylic acid and a 7-nitrosoindole. These compounds are useful as photolabile precursors of carboxylic acids, particularly neuroactive amino acids. The effect of electron-donating substituents at the 4-position has been explored for its effect on photolysis efficiency. 4-Methoxy substitution improved the photolysis efficiency >2-fold but the 4-dimethylamino analogue was essentially inert. A 5-alkyl substituent, that blocks unwanted nitration at this position, reduced the beneficial effect of the 4-methoxy group. (C) 2000 Elsevier Science Ltd.
