108861-47-8 Usage
Heterocyclic aromatic organic compound
1H-Indole is a compound with a ring structure containing both carbon and nitrogen atoms, which gives it aromatic properties.
Derivative of indole
The compound is derived from the indole structure by attaching additional functional groups to the ring.
Sulfonyl groups
The compound contains sulfonyl (-SO2-) groups attached to the 4-position and the 1-position of the indole ring, which can impart acidity and reactivity to the molecule.
Methylphenyl group
A methylphenyl (-C6H4CH3) group is attached to the 1-position of the indole ring, which can influence the compound's solubility and stability.
Unique chemical properties
The presence of the sulfonyl and methylphenyl groups gives the compound unique chemical properties, such as reactivity and solubility, that can be useful in various applications.
Potential applications
The compound has potential applications in fields such as pharmaceuticals, agrochemicals, and materials science due to its unique properties.
Synthesis through multi-step organic reactions
The compound can be synthesized through a series of chemical reactions, including sulfonation and alkylation of the indole ring, to attach the desired functional groups.
Check Digit Verification of cas no
The CAS Registry Mumber 108861-47-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,8,6 and 1 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 108861-47:
(8*1)+(7*0)+(6*8)+(5*8)+(4*6)+(3*1)+(2*4)+(1*7)=138
138 % 10 = 8
So 108861-47-8 is a valid CAS Registry Number.
108861-47-8Relevant articles and documents
A FACILE SYNTHESIS OF 4-(SULFONYLMETHYL)INDOLES FROM 4-OXO-4,5,6,7-TETRAHYDROINDOLE: FORMAL TOTAL SYNTHESIS OF 6,7-SECOAGROCLAVINE
Hatanaka, Naoto,Ozaki, Osamu,Matsumoto, Masakatsu
, p. 3169 - 3172 (2007/10/02)
A facile and short procedure for 4-(sulfonylmethyl)indole synthesis from 4-oxo-4,5,6,7-tetrahydroindole is developed and formal total synthesis of 6,7-secoagroclavine is completed to prove the versatility of this sulfone.
