108665-99-2 Usage
Derivative of indole
A heterocyclic aromatic organic compound based on the indole structure, with modifications to its chemical structure.
Tert-butyl group
A 1-methylethyl group attached to the indole ring, which is a bulky, non-reactive alkyl group.
Phenylsulfonyl group
A phenyl group (a ring of six carbon atoms with a double bond) attached to a sulfonyl group (a sulfur atom double-bonded to two oxygen atoms) that is attached to the indole ring.
Reactive functional group
The phenylsulfonyl group can participate in various synthetic transformations, making it a useful component in chemical reactions.
Potential applications
1H-Indole, 3-(1-methylethyl)-2-(phenylsulfonyl)may have possible uses in organic synthesis and pharmaceutical research.
Further study needed
More research is required to fully understand the properties and potential applications of this chemical compound.
Check Digit Verification of cas no
The CAS Registry Mumber 108665-99-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,6,6 and 5 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 108665-99:
(8*1)+(7*0)+(6*8)+(5*6)+(4*6)+(3*5)+(2*9)+(1*9)=152
152 % 10 = 2
So 108665-99-2 is a valid CAS Registry Number.
108665-99-2Relevant academic research and scientific papers
Unusual Reactions of Magnesium Indolates with Benzenesulfonyl Chloride
Wenkert, Ernest,Moeller, Peter D. R.,Piettre, Serge R.,McPhail, Andrew T.
, p. 3404 - 3409 (2007/10/02)
Grignard reagents from N-unsubstituted indoles and benzenesulfonyl chloride undergo reaction such as to produce unstable intermediates of β-chlorination and α-sulfonylation, which are transformed into oxindoles or substituted indoles.In the same reaction, yuehchukene (the naturally occurring dehydroprenylindole dimer) is converted into a spirooxindole, containing a strained four-membered ring, which is changed into a spirooxindole isomer with ring expansion on mild acid treatment.
