119340-97-5 Usage
Molecular structure
1H-Indole,4,6-dibromo-3-(methylsulfinyl)-2-(methylthio)-, (-)is a complex organosulfur compound with an indole ring as its core structure.
Substituents
The compound has two bromine atoms, a methylsulfinyl group, and a methylthio group attached to the indole ring.
Chirality
The compound exists in a chiral form, denoted as (-)-, which indicates its specific optical rotation properties.
Applications
1H-Indole,4,6-dibromo-3-(methylsulfinyl)-2-(methylthio)-, (-)is commonly used in organic chemistry research and drug discovery.
Unique features
The compound has unique structural features and potential pharmacological activities, making it an interesting subject for further studies.
Further research
More studies are needed to fully understand the biological effects and potential applications of 1H-Indole,4,6-dibromo-3-(methylsulfinyl)-2-(methylthio)-, (-)-.
Check Digit Verification of cas no
The CAS Registry Mumber 119340-97-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,3,4 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 119340-97:
(8*1)+(7*1)+(6*9)+(5*3)+(4*4)+(3*0)+(2*9)+(1*7)=125
125 % 10 = 5
So 119340-97-5 is a valid CAS Registry Number.
119340-97-5Relevant academic research and scientific papers
Tanaka, Jun'ichi,Higa, Tatsuo,Bernardinelli, Gerald,Jefford, Charles W.
, p. 7301 - 7310 (1989)
Six new polybromoindoles (9-14) have been isolated from the red alga Laurencia brongniartii.Two were optically active sulfoxides, the itomanindole A (12) and B (13) and one was a bisindole (14).The structures of 12 and 14 were elucidated by X-ray analysis.The sulfoxides 12 and 13 were readily converted with diazomethane to the corresponding N-methyl derivatives.Treatment with acetic anhydryde at room temperature gave the same indolenine (24) as the major product.
