88207-46-9 Usage
Indole derivative
A heterocyclic compound commonly found in natural products and pharmaceuticals The compound is based on the indole structure, which is a prevalent structure in many biologically active substances.
Bromophenyl group
A phenyl ring substituted with a bromine atom The presence of this group introduces a halogen atom into the molecule, which can influence reactivity and properties.
Phenylsulfonyl group
A phenyl ring attached to a sulfonyl group (-SO2-) This group imparts unique reactivity and properties to the compound, making it useful for various applications in organic synthesis and medicinal chemistry.
Potential applications
Organic synthesis, medicinal chemistry, drug discovery, and materials science The presence of the bromine and sulfonyl groups makes this compound a valuable building block for the development of new compounds with desired properties in various fields.
Unique reactivity and properties
Due to the presence of the bromine and sulfonyl groups, this compound may exhibit unique reactivity and properties that can be exploited for the development of new compounds with specific characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 88207-46-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,2,0 and 7 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 88207-46:
(7*8)+(6*8)+(5*2)+(4*0)+(3*7)+(2*4)+(1*6)=149
149 % 10 = 9
So 88207-46-9 is a valid CAS Registry Number.
88207-46-9Relevant articles and documents
Indole β-Nucleophilic Substitution. Part 7. β-Halogenation of Indoles. Attempted Intramolecular β-Nucleophilic Substitution of α-Arylindoles
Dalton, Lesley,Humphrey, Godfred L.,Cooper, Melanie M.,Joule, John A.
, p. 2417 - 2422 (2007/10/02)
Intramolecular β-nucleophilic substitution of 2-aryl-1-phenylsulphonylindoles could not be achieved.N-Arylsulphonylation of 2-arylindoles with arylsulphonyl halides using phase-transfer conditions is accompanied by 3-halogenation in some cases; the propor
