180633-67-4 Usage
Molecular structure
The compound contains an indole ring, which is a tricyclic aromatic system consisting of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring. The indole ring is the central core of the molecule.
3-Iodo group
The presence of the 3-iodo group, which is a halogen atom, confers certain properties to the molecule, such as increased electronegativity and the ability to participate in certain chemical reactions.
6-Methoxymethoxy group
The methoxymethoxy group is an ether functional group consisting of an oxygen atom bonded to two alkyl groups (methoxy). This group is electron-donating and can influence the reactivity of the molecule.
1-Phenylsulfonyl group
The phenylsulfonyl group is a sulfonyl functional group consisting of a sulfur atom bonded to a phenyl ring. This group is electron-withdrawing and can influence the reactivity of the molecule.
Uses
1H-Indole, 3-iodo-6-(methoxymethoxy)-1-(phenylsulfonyl)is used in organic synthesis and pharmaceutical research as a building block for creating new compounds with potential biological activity. Its unique structure and functional groups make it a valuable intermediate for the synthesis of diverse compounds with a range of properties and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 180633-67-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,0,6,3 and 3 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 180633-67:
(8*1)+(7*8)+(6*0)+(5*6)+(4*3)+(3*3)+(2*6)+(1*7)=134
134 % 10 = 4
So 180633-67-4 is a valid CAS Registry Number.
180633-67-4Relevant articles and documents
A three-component coupling approach to the marine bis-indole alkaloids: Topsentin, deoxytopsentin and bromotopsentin
Achab, Said
, p. 5503 - 5506 (2007/10/03)
The total syntheses of three marine bis-indole alkaloids (1, 2, 4) of the topsentin family together with the synthesis of unnatural deoxybromotopsentin (33) are described. Key elements include, a 1,2-addition-oxidation sequence to construct the bis-hetero
