114991-55-8 Usage
Chemical structure
The compound consists of a trifluoro group attached to a cyclohepta[b]indol-4-yl moiety, which is further connected to a methanesulfonamide group.
Unique structure
The compound has a highly specialized and complex structure, which may contribute to its potential applications in various scientific and industrial fields.
Chemical properties
The compound's chemical characteristics may make it suitable for use in research studies or as a reference compound in analytical chemistry.
Pharmacological properties
1,1,1-trifluoro-N-(5,6,7,8,9,10-hexahydrocyclohepta[b]indol-4-yl)methanesulfonamide may exhibit biological activities due to its unique structure, which could make it potentially useful in various applications.
Potential applications
The compound could be used as a building block in the synthesis of novel drug molecules, given its specific chemical and pharmacological properties.
Industrial relevance
Due to its specialized structure and potential applications, 1,1,1-trifluoro-N-(5,6,7,8,9,10-hexahydrocyclohepta[b]indol-4-yl)methanesulfonamide may have significant potential in various scientific and industrial fields.
Check Digit Verification of cas no
The CAS Registry Mumber 114991-55-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,9,9 and 1 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 114991-55:
(8*1)+(7*1)+(6*4)+(5*9)+(4*9)+(3*1)+(2*5)+(1*5)=138
138 % 10 = 8
So 114991-55-8 is a valid CAS Registry Number.
114991-55-8Relevant articles and documents
NUOVI DERIVATI DI 7-AMMINO-2,3-POLIMETILENINDOLI AD ATTIVITA ANTIINFIAMMATORIA
Cerri, R.,Pau, A.,Boatto, G.,Sparatore, F.,Satta, M.,Capasso, F.
, p. 91 - 102 (2007/10/02)
Thirthyfour new N-acylderivatives of 7-amino-2,3-polymethyleneindoles (I) and (II) were prepared and tested, together with a few analogues previously obtained, against carrageenan edema in the rat.Several compounds, at a dose of 1 mmole/kg, exhibit good inhibitory activity, that in some cases is superior to that displayed by indomethacin at a dose of 5 mg/kg.With only one exception, activity is confined to compounds of formula (I) and, generally, derivatives of 2,3-hexamethyleneindole are more active than those of lower homologues.
